C-P8XLChondrial Therapeutics
protein replacement therapy, intracellular delivery, fusion proteins
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C-P8XLC-P8XLprotein replacement therapy, intracellular delivery, fusion proteins
0-100 chain-logic scale · 15 dimensions · scored on public evidence
The goal of this clinical trial is to evaluate the safety and tolerability of nomlabofusp (CTI-1601) in adolescents and children with Friedreich's ataxia (FRDA).
An open label study designed to evaluate the safety, PK, PD, and clinical effects of long-term daily administration of CTI-1601 enrolling adolescent and adult patients with FRDA who have participated in a prior clinical study of CTI-1601 as well as children (age 2 years and older), adolescents and adults with FRDA who have not participated in a prior clinical study of CTI-1601.
To evaluate the safety and tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of subcutaneous (SC) administration of CTI-1601 over 28 days in subjects with Friedreich's ataxia (FRDA).
To examine range of tissue frataxin (FXN) concentrations, specific ribonucleic acids, other proteins and specialized lipids in the buccal cells, blood, and skin cells of normal healthy volunteers without Friedreich's ataxia (FRDA).
To evaluate the safety and tolerability of multiple ascending doses of CTI-1601 in participants with Friedreich's ataxia
To test the variability of specific ribonucleic acid (RNA) and proteins as well as frataxin levels in samples of blood and buccal cells taken directly from patients with Friedreich's ataxia (FRDA) in order to confirm potential new biomarkers of disease in patients with FRDA.
To evaluate the safety and tolerability of single ascending doses of CTI-1601 in participants with Friedreich's ataxia
Joseph Truitt – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Care
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Larimar seeks 2026 votes and higher share authorization | LRMR Proxy Statement --> STOCK TITAN Login Sign up Login Sign up 0 HOME --> NEWS FEED Stock News Live Stock News Today Trending News AI news FDA Approvals Clinical Trials Crypto News Merger & Acquisitions Earnings Offerings IPO News Stock Splits Top News - Gainers Top News - Losers SEC FILINGS SEC Filings Live SEC Filings Today Form 4 - Insider Trading 8-K - Material Events 10-K - Annual Reports 10-Q - Quarterly Reports DEF 14A - Proxy Statements S-1 - IPO Registration S-3 - Shelf Registration STOCKS All Stock Themes AI Stocks Crypto St … holders to vote at its virtual 2026 Annual Meeting on May 19, 2026, including a proposal to amend its charter to increase authorized common stock from 115,000,000 to 215,000,000 shares. Stockholders will also vote on electing three Class III directors through 2029, advisory approvals of executive compensation and its voting frequency, ratifying PricewaterhouseCoopers as auditor for 2026, and a potential adjournment if there are insufficient votes for the share increase. The p … Designation, alignment under the START pilot program toward a Biologics License Application using skin FXN as a surrogate endpoint, and positive long‑term open‑label data. It also notes two underwritten equity offerings in 2025–2026 raising roughly $65.0 million and $107.6 million in net proceeds, director and executive pay structures with a high proportion of at‑risk, performance‑based compensation, and a largely independent, six‑member staggered board with separate chair an … ndment Proposed authorized common stock 215,000,000 shares Charter amendment in Proposal 5 Shares outstanding 103,882,937 shares Common stock outstanding as of March 25, 2026 record date July 2025 equity offering 21,562,500 shares; $65.0 million net Underwritten public offering of common stock February 2026 equity offering 23,000,000 shares; $107.6 million net Underwritten public offering of common stock 2025 audit and related fees $801,000 PwC audit and all other fees for fi … 5 corporate goals Key Terms Breakthrough Therapy Designation, Biologics License Application, performance-based restricted stock units, broker non-vote, +2 more 6 terms Breakthrough Therapy Designation regulatory "In February 2026, we announced the FDA granted Breakthrough Therapy Designation to nomlabofusp for the treatment of adults and children
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Chondrial Therapeutics Announces Development Milestone — Cure FA Foundation Home 2016 Gala Our Story About What is FA? CURE FA Mission-Vision CHOP/UPENN FA Center of Excellence Cure FA Foundation Strategies Cure FA Board of Directors Contact News Partners FARA Chondrial Therapeutics Take Action Home 2016 Gala Our Story About What is FA? CURE FA Mission-Vision CHOP/UPENN FA Center of Excellence Cure FA Foundation Strategies Cure FA Board of Directors Contact News Partners FARA Chondrial Therapeutics Take Action Rudolph McCormick June 20, 2016 Chondrial Therapeutics Announces Development M … ondrial Therapeutics. Their goal is to enable an Investigational New Drug (IND) application, advance TAT-Frataxin into Phase I trials, and ultimately deliver a therapy for this debilitating orphan disease. FA is a rare inherited disease that causes nervous system damage and movement problems. Usually beginning in childhood, it leads to impaired muscle coordination that worsens over time. “We are excited about being selected into this prestigious program”, said Steven Pl
Drug developed at IU enters clinical trial Skip to main content Indiana University School of Medicine Indiana University School of Medicine Menu Expertise Toggle Sub-navigation Alzheimer's Disease Indiana Health Precision Health Initiative Musculoskeletal Health Traumatic Brain Injury Global Health LGBTQ+ Health Education Toggle Sub-navigation MD Program Graduate Medical Education Graduate Degrees Dual Degrees Health Professions Programs Continuing Education Point of Care Ultrasound Medical Library Mental Health Services Research Toggle Sub-navigation Our Impact Centers Institutes Clinical … ion Faculty Giving Global Health Indiana Health Research Findings Past Releases Submit News Media Coverage Media Relations Contacts Faculty Drug developed at IU enters clinical trial Dec 30, 2019 Lab Details 16 A drug molecule that was developed in an Indiana University School of Medicine laboratory has just been administered to its first round of patients. Chondrial Therapeutics Inc., a clinical-stage biotechnology company co-founded by IU School of Medicine Professor of Ped … 02 [email protected] Contact Us Additional resources Popular Topics MD Admissions Residency Programs PhD Fact Sheet Alumni MedNet Contact Indiana University School of Medicine 340 West 10th Street Fairbanks Hall, Suite 6200 Indianapolis, IN 46202-3082 317-274-8157 [email protected] Social media Facebook Facebook Instagram Instagram LinkedIn LinkedIn Twitter Twitter Indiana University School of Medicine Accessibility Help Privacy Policy Copyright © 2026 The Trustees of Indian
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Chondrial Therapeutics Announces Dosing of First Patients in Phase 1 Clinical Program of CTI-1601 for Treatment of Friedreich’s Ataxia - Friedreich's Ataxia Research Alliance Skip to main content Accessibility Search Understanding FA What is Friedreich’s ataxia? Signs and Symptoms Journey to an FA Diagnosis Genetics of FA Treating and Managing FA Newly Diagnosed What You Need to Know Connect with Others in the Community Managing FA Clinical Management Guidelines Assembling a Care Team Treatment for FA Approved Treatments For Healthcare Professionals Terms to Know (Glossary) Research Grant … ts For Healthcare Professionals Terms to Know (Glossary) Research Grant Program Grant Application Process Grant Types FARA Funded Grants Grant Priorities Opportunities for Young Investigators Research Resources Research and Drug Development Tools Scientific Conferences Regulatory Interactions Research Initiatives FA Global Clinical Consortium FARA Directed Research Institutional Supported Programs Drug Development Pipeline Participate in Research Clinical Trial Finder Underst … 601 that can be redeemed to receive a priority review of a subsequent marketing application. Additional information on the trial can be found on www.clinicaltrials.gov using the identifier NCT04176991. About Friedreich’s Ataxia Friedreich’s ataxia (FA) is a debilitating, life-shortening, progressive rare genetic disease that affects multiple body systems, particularly the brain and heart. It is the most common ataxia and is caused by a deficiency of a key protein, frataxin, w … You should not place undue reliance on these forward-looking statements, which apply only as of the date of this communication. Chondrial expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in its expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based . Media Contact: Krystle Gibbs Ten Bridge … ; Press FARA Store Policies Terms and Conditions Informed Stay Informed Captcha Submit If you are human, leave this field blank. Follow us © 2026 . Friedreich's Ataxia Research Alliance. Accessibility Sitemap Cookie Preferences Site by Rouge
Chondrial Therapeutics — Cure FA Foundation Home 2016 Gala Our Story About What is FA? CURE FA Mission-Vision CHOP/UPENN FA Center of Excellence Cure FA Foundation Strategies Cure FA Board of Directors Contact News Partners FARA Chondrial Therapeutics Take Action Home 2016 Gala Our Story About What is FA? CURE FA Mission-Vision CHOP/UPENN FA Center of Excellence Cure FA Foundation Strategies Cure FA Board of Directors Contact News Partners FARA Chondrial Therapeutics Take Action Partners FARA Chondrial Therapeutics Normal 0 false false false EN-US X-NONE X-NONE Chondrial Therapeutics LLC
Fighting Friedreich’s ataxia: A pediatric cardiologist’s journey of innovation and collaboration | Friedreich's Ataxia Research Alliance (FARA) LinkedIn respects your privacy LinkedIn and 3rd parties use essential and non-essential cookies to provide, secure, analyze and improve our Services, and to show you relevant ads (including professional and job ads ) on and off LinkedIn. Learn more in our Cookie Policy . Select Accept to consent or Reject to decline non-essential cookies for this use. You can update your choices at any time in your settings . Accept Reject Agree & Join LinkedIn By
#IARC 2017 - FA Clinical Trial Possible Next Step for Chondrial's Protein Replacement Therapy Skip to content Newsletter Search Search for: Search Toggle navigation Search for: Search About FA Toggle menu: About FA What is FA? Causes Symptoms Diagnosis Life expectancy Treatments Approved treatment: Skyclarys Experimental Treatments Non-drug Treatments Living with Toggle menu: Living with Living with FA Exercise and physiotherapy Diet Occupational therapy Speech therapy Adaptive equipment Late-onset FA Mental health Support and resources Community Toggle menu: Community Perspectives Defini
XML 24 R15.htm IDEA: XBRL DOCUMENT v3.22.2.2 Related Party Transactions 9 Months Ended Sep. 30, 2022 Related Party Transactions [Abstract]   Related Party Transactions 9. Related Party Transactions In November 2016, the Company entered into a consulting agreement with Mark Payne, M.D (the “Consulting Engagement”). Dr. Payne was a director of Chondrial Therapeutics, Inc. ("Chondrial") at that time. Chondrial was the name of the Company prior to its merger with Zafgen in May 2020. Dr. Payne was, and continues to be, a full-time employee of IU and one of the inventors of the lice
Scientific Advisory Board – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisor
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Nomlabofusp_beta – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board C
Mark Payne, MD – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Car
Leadership – Page 2 – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisor … sity of Pennsylvania and her MD from Jefferson Medical College. She completed a residency in internal medicine and a fellowship in nephrology. Posts navigation Newer posts Search for: Recent Comments Archives Categories No categories Meta Log in Entries feed Comments feed WordPress.org © 2026 Larimar Therapeutics, Inc. All rights reserved. LARIMAR and LARIMAR THERAPEUTICS are trademarks of Larimar Therapeutics, Inc. Terms of Use Privacy Policy Site Credits
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#eoyph | Larimar Therapeutics Inc. LinkedIn respects your privacy LinkedIn and 3rd parties use essential and non-essential cookies to provide, secure, analyze and improve our Services, and to show you relevant ads (including professional and job ads ) on and off LinkedIn. Learn more in our Cookie Policy . Select Accept to consent or Reject to decline non-essential cookies for this use. You can update your choices at any time in your settings . Accept Reject Agree & Join LinkedIn By clicking Continue to join or sign in, you agree to LinkedIn’s User Agreement , Privacy Policy , and Cookie Policy … Dr. Carole Ben-Maimon as an Entrepreneur Of The Year® 2020 Greater Philadelphia award winner! Stay tuned as Dr. Ben-Maimon advances to the Entrepreneur Of The Year® US virtual awards event in November. #EOYPH 36 4 Comments Like Comment Share Copy LinkedIn Facebook X Greg Griesemer 5y Report this comment Congrats Carole, well deserved! Like Reply 1 Reaction Denis B. 5y Report this comment Absolutely deserving, congrats Carole. Like Reply 1 Reaction Nicole Matz 5y Rep
Carole Ben-Maimon, MD – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Bo … sity of Pennsylvania and her MD from Jefferson Medical College. She completed a residency in internal medicine and a fellowship in nephrology. Back to Board of Directors > © 2026 Larimar Therapeutics, Inc. All rights reserved. LARIMAR and LARIMAR THERAPEUTICS are trademarks of Larimar Therapeutics, Inc. Terms of Use Privacy Policy Site Credits
Press Release Distribution and Management Accessibility: Skip TopNav Latest News and Press Releases Want to stay updated on the latest news? Sign into Reader Account Create Reader Account June 26, 2026 16:05 ET | Source: Larimar Therapeutics Larimar Therapeutics Announces Investor Event on the Nomlabofusp Program for Friedreich’s Ataxia Webcast on Monday, June 29, 2026, at 7:45 am ET BALA CYNWYD, Pa., June 26, 2026 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (Larimar) (Nasdaq: LRMR), a clinical-stage biotechnology company... May 14, 2026 07:00 ET | Source: Larimar Therapeutics Larima … Reports First Quarter 2026 Financial and Business Update Intending to initiate rolling BLA seeking accelerated approval with submission of nonclinical and clinical modules in June 2026; submission of the final modules including the CMC module expected in... April 30, 2026 16:05 ET | Source: Larimar Therapeutics Larimar Therapeutics Publishes Cross-Species Findings Supporting Skin as a Surrogate for the Measurement of Frataxin in Tissues Clinically Relevant to Friedreich’s At
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Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar Therapeutics Shares New Phase 1 and Phase 2 Data on Nomlabofusp at ICAR 2024 Products Data Feature Plans Request Demo Sign Up for Free Larimar Therapeutics Shares New Phase 1 and Phase 2 Data on Nomlabofusp at ICAR 2024 3 December 2024 Larimar Therapeutics , a clinical-stage biotechnology company, recently showcased data from their Phase 1 and Phase 2 studies of nomlabofusp at the International Congress for Ataxia Research (ICAR) in London. The studies involved 61 adults with Friedreich’s ataxia (FA) and examined the effects of subcutaneous administration of nomlabofusp in doses rangin … ed approval using FXN levels as a novel surrogate endpoint. The company aims to submit a Biologics License Application (BLA) by the second half of 2025, with a program update anticipated in mid-December 2024. Dr. Rusty Clayton, Larimar's Chief Medical Officer, expressed satisfaction with the consistency of the relationships between tissue FXN levels and disease characteristics in FA patients across their studies. The data supports the dose prediction modeling used to select a
Larimar Therapeutics Reports First Quarter 2025 Financial Results - The Globe and Mail Home Canada Business Investing Life Opinion World Politics Personal Finance Culture Sports More More Latest in More Real Estate Drive Watchlist For You Events Find clarity in the chaos. Subscribe now and save 70% Subscribe Digital access Digital + home delivery TSX 0.19 % S&P 500 -0.12 % DOW -0.13 % NASDAQ -0.31 % Oil -3.98 % Dollar 0.08 % Gold 0.82 % tsx movers: BB-T + 8.28 % CNQ-T + 0.18 % HIVE-T + 7.09 % KEEL-T + 3.02 % This section contains press releases and other materials from third parties (inclu … dback and recommendations in line with our current approach, we are on track to submit our planned Biologics License Application (BLA) by the end of 2025 to seek accelerated approval,” said Carole Ben-Maimon, MD, President, and Chief Executive Officer of Larimar. “We continue to have frequent communication with the FDA via our START pilot program participation including interactions regarding the adequacy of the safety data set required to support BLA submission. In mid-2025 … as an RLSE to support approval will be a matter of review in a future marketing application. FDA recommended focusing on assessments of skin FXN concentrations and acknowledged that submitted data appear to support a relationship between increased FXN concentrations in skin cells and relevant tissues such as the heart, dorsal root ganglion, and skeletal muscle. FDA also acknowledged that the nonclinical studies we submitted were performed at relevant human doses. FDA suggeste … ential sites in the U.S., Europe, U.K., Canada, and Australia. Larimar plans to submit the BLA submission seeking accelerated approval by the end of 2025 to seek accelerated approval. First Quarter 2025 Financial Results As of March 31, 2025, the Company had cash, cash equivalents and marketable securities totaling $157.5 million. The Company reported a net loss for the first quarter of 2025 of $29.3 million, or $0.46 per share, compared to a net loss of $14.7 million, or $0. … nstitute Contact us Address and Phone Number Standards Editors Staff SecureDrop Submit an article Reader services Account Settings Customer Support Subscriptions Member Benefits Privacy Settings About us Company information Work at The Globe Accessibility Editorial Code of Conduct Sustainability Licensing & Permissions Election Advertising Re
Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
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Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
FARA - Larimar Therapeutics Reports Positive Top-line Data... Facebook Log In FARA's Post FARA February 12, 2024 · Shared with Public Larimar Therapeutics Reports Positive Top-line Data from Phase 2 Dose Exploration Study from 25 mg and 50 mg Cohorts of Nomlabofusp in Patients with Friedreich’s Ataxia: -Nomlabofusp was generally well tolerated following repeated subcutaneous injections in patients in the 25 and 50 mg cohorts with no serious adverse events -Dose dependent increases in frataxin levels were observed in skin and buccal cells -Open Label Extension (OLE) study initiated in Janu … n levels as a novel surrogate endpoint to support a potential Biologics License Application (“BLA”) submission for accelerated approval targeted for 2H 2025 The company management will host a webcast and conference call today, February 12, 2024 at 8:00 a.m. ET. Click here to read the full press release: https://bit.ly/49bTrlc Click here to access the webcast: https://bit.ly/48mkp8Q All reactions: 82 15 shares Like Comment
Interim observations from a long-term open label study evaluating daily nomlabofusp administration in patients with Friedreich’s ataxia - MDA Clinical & Scientific Conference 2026 and tags on every page of your site. --> Register Now --> Home MDA Conference 2026 Registration Rates Agenda Location & Venue Our Sponsors CE Media Information Sponsorships & Exhibits Sponsorship Levels Event Sponsorships Marketing Sponsorships Exhibit Information Patient Advocacy Pavilion Abstracts 2026 Abstract Guidelines 2026 Abstract Library 2025 Abstract Library 2024 Abstract Library 2023 Abstract … Demand Conference About Us About The MDA Conference About MDA Awards MDA Legacy Award for Achievement in Clinical Research The MDA Donavon Decker Community Impact in Research Award MDA Research Momentum Award Future Conferences Contact Us Home MDA Conference 2026 Registration Rates Agenda Location & Venue Our Sponsors CE Media Information Sponsorships & Exhibits Sponsorship Levels Event Sponsorships Marketing Sponsorships Exhibit Information Patient Advocacy Pavilio … Demand Conference About Us About The MDA Conference About MDA Awards MDA Legacy Award for Achievement in Clinical Research The MDA Donavon Decker Community Impact in Research Award MDA Research Momentum Award Future Conferences Contact Us Interim observations from a long-term open label study evaluating daily nomlabofusp administration in patients with Friedreich’s ataxia Topic: Clinical Trials Poster Number: 419 O Author(s): Russell Clayton, DO, Larimar Therapeutics Inc., Er
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Publications – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Caree
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Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scient
Larimar details progress on FA drug nomlabofusp | LRMR Annual Report (10-K) --> STOCK TITAN Login Sign up Login Sign up 0 HOME --> NEWS FEED Stock News Live Stock News Today Trending News AI news FDA Approvals Clinical Trials Crypto News Merger & Acquisitions Earnings Offerings IPO News Stock Splits Top News - Gainers Top News - Losers SEC FILINGS SEC Filings Live SEC Filings Today Form 4 - Insider Trading 8-K - Material Events 10-K - Annual Reports 10-Q - Quarterly Reports DEF 14A - Proxy Statements S-1 - IPO Registration S-3 - Shelf Registration STOCKS All Stock Themes AI Stocks Crypto Stock … y offering added $107.6 million in net proceeds, which together are expected to fund operations into the second quarter of 2027. Positive None. Negative None. Insights Biotech pipeline and regulatory strategy analyst neutral High-option FA program, clear milestones, but still binary risk. Larimar Therapeutics centers on nomlabofusp, a frataxin protein replacement for Friedreich’s ataxia. The program benefits from Orphan, Fast Track, Breakthrough Therapy, PRIME and ILAP design … eding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐ Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company” and “emerging growth company̶ … and completion of clinical trials, the timing of a potential Biologics License Application (“BLA”) submission to the FDA or similar applications to be submitted to other countries for accelerated approval, including our ability to supply to the FDA or to regulatory authorities in other countries all required data for the FDA to review and accept an accelerated application, or any other product candidates that we may develop in the future; • the difficulties … ation and labeling under any such approval; • how long we can continue to fund our operations with our existing cash, cash equivalents and marketable securities and our estimates regarding future results of operations, financial position, research and development costs, capital requirements and our access and needs for additional financing;
Speaker Highlight: Tom Daniel, MD - Technology Summit at Scripps Research - The Scripps Research Institute Skip to the content Register 2026 Agenda 2025 Summit Recap Strategic Investment Committee FAQ Register 2026 Agenda 2025 Summit Recap Strategic Investment Committee FAQ Speaker Spotlight Tom Daniel, MD Board member, Scripps Research Throughout a multifaceted career, he has helped advance healthcare as a physician, researcher, educator and business leader. Tom brings more than 20 years of experience leading and building research and development organizations and leading investments in new c … zations and leading investments in new companies at the forefront of innovative application of science to healthcare. Recently he served as a Venture Partner at ARCH Venture Partners for five years following a decade as President of Global Research and Early Development at Celgene Corporation. He previously served in senior leadership roles at AmbRx, Amgen and Immunex. Tom was formerly a director at Juno, Epizyme, Sana, Larimar and Vir. He currently serves as board chair at L … Texas, Southwestern, he trained in molecular genetics at UTSW and completed his residency in Internal Medicine at Massachusetts General Hospital. True to his physician roots, thoughts of the countless patients awaiting the translation of scientific progress are never far from Daniel’s mind. “The most powerful inspiration for my early career was watching medical advances stay a half step ahead of my father’s cardiovascular disease, thereby sustaining his life for over 40 years
Larimar Therapeutics Inc (LRMR) News, Articles, Events & Latest Updates Use App Trending News Earnings All DIA 0.22% SPY 0.49% QQQ 1.56% Trending MSTR 4.02% BE 17.14% USO 1.78% SRPT 5.49% IBRX 10.14% CRML 6.91% CAPR 12.17% ARDX 7.59% FUBO 20.03% LCID 13.09% MSTR 4.02% BE 17.14% USO 1.78% SRPT 5.49% IBRX 10.14% CRML 6.91% CAPR 12.17% ARDX 7.59% FUBO 20.03% LCID 13.09% Feed News Sentiment Earnings Fundamentals Info home Symbol LRMR news Exchange: NASDAQ · Updated 05:14 PM EDT LRMR Larimar Therapeutics Inc $3.76 $0.16 (4.57%) Today · Closed $3.66 $0.10 (2.73%) After Hours 4 , 9 4 8 4 , 9 4 8
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--> Larimar Therapeutics Welcomes Dr. Jeffery Sherman - LRMR | BioPha --> Login Start Free Trial Catalyst Calendar FDA Calendar Track key readouts and FDA decision dates in biotech and pharma. BPW Portfolio Bio Hedge Fund Shots and more... Historical FDA Calendar Review past FDA decisions and clinical readouts. Market Movers Track today's biotech market movers Biotech Earning Calendar Stay updated on biotech earnings. Historical PDUFA Dates Review past PDUFA dates and decisions. PDUFA Calendar Stay ahead of upcoming PDUFA dates Conference Calendar Keep up with biotech events. IPO Upcoming & … p; past IPOs. Bio Pharma Screener Catalyst Sync™ Track biotech catalysts. Hedge Fund Screener Analyze hedge fund holdings. Company Screener Holistic company & pipeline analysis. All Stocks Holdings Explore hedge fund stock data. Heat-Map Market size & sector heat map. Inside Trades Monitor insider trading. Biotech Analyst Ratings Biotech analyst ratings & price targets M&A Tracker Track M&A deals and acquisition targets Resources News Latest biotech news. … iversity of Medicine and Science and completed an internal medicine internship, residency, and chief medical residency at Northwestern University. His fellowship training was at the University of California, San Francisco, where he was also a research associate at the Howard Hughes Medical Institute. About Larimar Therapeutics Larimar Therapeutics, Inc. (Nasdaq: LRMR), is a clinical-stage biotechnology company focused on developing treatments for complex rare diseas
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Tietosuojavalintasi guce guce Tietosuojasi on meille tärkeää Tietosuojavalintojasi käytetään kaikissa Yahoo-konsernin tarjoamissa sivustoissa ja sovelluksissa. Yahoo käyttää evästekäytännöstämme ."> Evästeet Evästeiden (sekä vastaavien tekniikoiden, esimerkiksi verkkotallennuksen) avulla verkkosivustojen sovellusten ylläpitäjät voivat tallentaa ja lukea laitteesi tietoja. Lue lisää evästekäytännöstämme . evästeitä seuraaviin tarkoituksiin: tarjotaksemme sivustomme ja sovelluksemme sinulle todentaaksemme käyttäjät, estääksemme roskapostia ja väärinkäytöksiä sekä toteuttaaksemme tietoturvatoimia
Francis Michael Conway, CPA – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advis
Board of Directors – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board … iversity of Medicine and Science and completed an internal medicine internship, residency, and chief medical residency at Northwestern University. His fellowship training was at the University of California, San Francisco, where he was also a research associate at the Howard Hughes Medical Institute. Joseph Truitt currently serves as the Chief Executive Officer (CEO) and Board Director of iECURE, Inc. Mr. Truitt previously was CEO of BioSpecifics Technologies Corp., which was … Arbor. Peter Barrett, PhD, joined Atlas Venture, an early-stage venture capital fund, in 2002, and currently serves as a Partner in the Life Sciences Group. Previously, from 1998 to 2002, he was a Co-founder, Executive Vice President and Chief Business Officer of Celera Genomics. Prior to Celera, from 1979 to 1998, Dr. Barrett held senior management positions at Perkin-Elmer Corporation, most recently serving as Vice President, Corporate Planning and Business Development. Dr. … ness School and is the Faculty Chair of the Key Advisory Board of the Blavatnik Fellowship Program. Dr. Barrett holds a B.S. in chemistry from Lowell Technological Institute (now known as the University of Massachusetts, Lowell) and a Ph.D. in analytical chemistry from Northeastern University. He also completed Harvard Business School’s Management Development Program. Jonathan Leff is a Partner on the Therapeutics team at Deerfield and Chairman of the Deerfield Institute, and … sity of Pennsylvania and her MD from Jefferson Medical College. She completed a residency in internal medicine and a fellowship in nephrology. Search for: Recent Comments Archives Categories No categories Meta Log in Entries feed Comments feed WordPress.org © 2026 Larimar Therapeutics, Inc. All rights reserved. LARIMAR and LARIMAR THERAPEUTICS ar
Leadership – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers … or the commercial launch of tab-cel® and played a key role in Biologics License Application (BLA) activities. Her scope of work included oversight of vendors, case management, database strategy and implementation, safety data exchange agreements, PV inspection readiness, and staff training. Earlier in her career, Dr. Saad spent several years at Johnson & Johnson, progressing to the role of Americas PV Head. In that role, she was responsible for ensuring PV compliance acro … D team that contributed to more than 60 combined investigational new drug (IND) application, biologics license application (BLA), and marketing authorization application (MAA) filings. He also previously worked as Senior Director and Head, Bioanalytical Sciences and Immunogenicity at Janssen Research & Development. Earlier in his career, Dr. Shankar worked as a Director, Immune Response Assessment and Research at Centocor R&D (a wholly-owned subsidiary of Johnson & … cal Scientists (AAPS) and was previously awarded the AAPS Distinguished Service Award. He also received several leadership and innovation awards, including two of Johnson & Johnson’s top recognitions – the Philip B. Hoffman Research Scientist Award and the SPARK Innovation Award. He has an Executive MBA from Drexel University, a Master of Science from Oklahoma State University, and a PhD from the University of Kentucky. Mohamed Hamdani joined Larimar Therapeutics in
8-K 1 d936040d8k.htm 8-K 8-K UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, DC 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported): May 28, 2020 Larimar Therapeutics, Inc. (Exact name of registrant as specified in its charter) Delaware 001-36510 20-3857670 (State or other jurisdiction of incorporation or organization) (Commission File Number) (I.R.S. Employer Identificat … 148;) with the SEC within 30 days following the Closing (the “Registration Deadline”) to register the Shares and the Warrant Shares. If the Company fails to meet the Registration Deadline or maintain the effectiveness of the Registration Statement for the required effectiveness period, subject to certain permitted exceptions, the Company will be required to pay liquidated damages to the Purchasers. The Company also agreed, among other things, to indemnify the sellin … remain exercisable subject to the terms and conditions of the applicable option award agreement. Peter Barrett, Ph.D., Thomas O. Daniel, M.D. and Frank E. Thomas continued as directors of the Company after the Merger. Appointment of Directors In connection with the Merger, the size of the Board was decreased from eight to seven members. In accordance with the Merger Agreement, on May 28, 2020, effective immediately after the effective time of the Merger, the following in … May 2018. Dr. Barrett joined Atlas Venture, an early-stage venture capital fund, in 2002, and currently serves as a Partner in the Life Sciences Group. Previously, from 1998 to 2002, he was a Co-Founder, Executive Vice President and Chief Business Officer of Celera Genomics (“Celera”). Prior to Celera, from 1979 to 1998, Dr. Barrett held senior management positions at Perkin-Elmer Corporation, most recently serving as Vice President, Corporate Planning and … ness School and is the Faculty Chair of the Key Advisory Board of the Blavatnik Fellowship Program. Dr. Barrett holds a B.S. in chemistry from Lowell Technological Institute (now known as the University of Massachusetts, Lowell) and a Ph.D. in analytical chemistry from Northeastern University. He also completed Harvard Business School’s
Frank E. Thomas – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Ca
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Larimar Therapeutics Strategy and Business Model Skip to content Skip content FIND YOUR CONSULTANT JOIN OUR COMMUNITY Services Strategy Operations Organization Marketing Finance Sales Artificial Intelligence (AI) Interim/Fractional Executives Enterprise Resource Planning (ERP) Associate-level Support Board Recruiting Pro bono Industries Resources Locations Insights Podcast Blog Books by members Umbrex Presents PowerPoint Templates About What we do Consultant directory Press Contact For consultants Join our Community How to start your own practice Events Resources Podcast Members’ forum U … ur own practice Events Resources Podcast Members’ forum Umbrex Consulting Fellowship Consultant directory Services Strategy Operations Organization Marketing Finance Sales Artificial Intelligence (AI) Interim/Fractional Executives Enterprise Resource Planning (ERP) Associate-level Support Board Recruiting Pro bono Industries Resources Locations Insights Podcast Blog Books by members Umbrex Presents PowerPoint Templates About What we do Consultant directory Press Contact … ur own practice Events Resources Podcast Members’ forum Umbrex Consulting Fellowship Consultant directory FIND YOUR CONSULTANT JOIN OUR COMMUNITY Services Strategy Operations Organization Marketing Finance Sales Artificial Intelligence (AI) Interim/Fractional Executives Enterprise Resource Planning (ERP) Associate-level Support Board Recruiting Pro bono Industries Resources Locations Insights Podcast Blog Books by members Umbrex Presents PowerPoint Templates About What … ur own practice Events Resources Podcast Members’ forum Umbrex Consulting Fellowship Consultant directory Services Strategy Operations Organization Marketing Finance Sales Artificial Intelligence (AI) Interim/Fractional Executives Enterprise Resource Planning (ERP) Associate-level Support Board Recruiting Pro bono Industries Resources Locations Insights Podcast Blog Books by members Umbrex Presents PowerPoint Templates About What we do Consultant directory Press Contact … ur own practice Events Resources Podcast Members’ forum Umbrex Consulting Fellowship Consultant directory Company Profiles > Larimar Therapeutics Strategy and Business Model Larimar Therapeutics Strategy and Business Model Executive Overview Larimar Therapeutics is a clinical-stage biopharmaceutical company focused on Friedreich’s ataxia
Nomlabofusp (CTI-1601) - Friedreich's Ataxia Research Alliance Skip to main content Accessibility Search Understanding FA What is Friedreich’s ataxia? Signs and Symptoms Journey to an FA Diagnosis Genetics of FA Treating and Managing FA Newly Diagnosed What You Need to Know Connect with Others in the Community Managing FA Clinical Management Guidelines Assembling a Care Team Treatment for FA Approved Treatments For Healthcare Professionals Terms to Know (Glossary) Research Grant Program Grant Application Process Grant Types FARA Funded Grants Grant Priorities Opportunities for Young Inves … it secured up to $22.6 million in Series A financing with plans to file an IND application for CTI-1601 (TAT-FXN) with FDA in order to initiate Phase 1 clinical trials of the compound. Chondrial Therapeutics also received Orphan Drug Designation for CTI-1601. Clinical Development: Phase I In November 2019 , Chondrial Therapeutics began a first-in-human study of CTI-1601 (previously known as TAT-frataxin, now formally named nomlabofusp) , a Phase I single ascending dose (SAD) … s. The results may also support the US regulatory filing (the Biologics License Application or BLA submission) for approval of the drug. In May 2024 , the FDA lifted the remaining partial hold , allowing use of 50 mg in the OLE. On May 30, 2024 , Larimar was selected by the FDA to participate in the START Pilot Program , a milestone-driven initiative to accelerate therapies for rare diseases. Nomlabofusp was selected based on its potential benefit in FA and the program’s read … he FDA agreed with the modifications of the dose regime. Larimar is planning to submit a BLA by mid-2026 . News and Press Releases News | Apr 6, 2026 Webinar Recording: Larimar Therapeutics March 2026 Update FARA News, Industry News Read Story News | Feb 24, 2026 Larimar Therapeutics Announces FDA Breakthrough Therapy Designation for Nomlabofusp in FA and Reiterates Planned BLA Submission in June 2026 Industry News Read Story News | Sep 29, 2025 Larimar Therapeutics Announces … ; Press FARA Store Policies Terms and Conditions Informed Stay Informed Captcha Submit If you are human, leave this field blank. Follow us © 2026 . Friedreich's Ataxia Research Alliance. Accessibility Sitemap Cookie Preferences Site by Rouge
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FARA - Larimar Therapeutics, Inc. announced today,... Facebook Log In FARA's Post FARA February 24 · Shared with Public Larimar Therapeutics, Inc. announced today, February 24, 2026, that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD) to nomlabofusp, a frataxin (FXN) protein replacement therapy for the treatment of adults and children with Friedreich’s ataxia (FA). Additionally, after a recent Support for Clinical Trials Advancing Rare Disease Therapeutics (START) pilot program meeting with FDA, the Company announced continued alignment with … nably likely to predict clinical benefit to support a planned Biologics License Application (BLA) submission seeking accelerated approval. The planned BLA submission is targeted for June 2026. Breakthrough Therapy Designation is intended to expedite the development and regulatory review of a drug intended to treat a serious condition. Larimar reported that FDA is aligned with plans to have the global confirmatory Phase 3 study underway at the time of BLA submission. Larimar w
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Zafgen and Chondrial Therapeutics Complete Reverse Merger and Begin Operating as Larimar Therapeutics | News & Events | Goodwin Skip to main content Goodwin Expertise People Careers Legal Paralegal Science Advisor Global Operations Team Insights & Resources About Us Our Story The Goodwin Way Opportunity, Inclusion, and Belonging Pro Bono Firm Leadership Locations News & Events Alumni Press Release June 4, 2020 Zafgen and Chondrial Therapeutics Complete Reverse Merger and Begin Operating as Larimar Therapeutics Professionals Danielle M. Lauzon Mitchell S. Bloom Tevia K. Pollard Sara … va Launches AHZANTIVE® Aflibercept Biosimilar in Europe Alert June 22, 2026 SEC Proposal Could Eliminate Baby Shelf Restrictions and Expand ATM Program Access For Smaller Companies Alert June 18, 2026 Delaware is Enforcing Its Principal Place of Business Requirement: An Inaccurate Address Can Block Good Standing Certificates Insight June 18, 2026 Royalty Monetization in an Era of Drug Pricing Pressure: How the IRA is Affecting Royalty Monetizations Big Molecule Watch June 16,
EX-10.2 4 lrmr-ex10_2.htm EX-10.2 EX-10.2 IU Agreement No. 2022-0109 THIRD AMENDMENT TO LICENSE AGREEMENT   This Third Amendment (the “Third Amendment”) is made and entered into as of June 9, 2022 (the “Third Amendment Effective Date”) by and between:   The Trustees of Indiana University (“IU”), a body politic and corporate of the State of Indiana, having its principal offices at 107 S. Indiana Ave., Bloomington, IN 47405; and   Larimar Therapeutics, Inc. (“Larimar”), a corporation organized under the laws of Delaware, havi
FARA - A reminder to join Larimar Therapeutics for an... Facebook Log In FARA's Post FARA March 17 · Shared with Public A reminder to join Larimar Therapeutics for an informational webinar for people living with FA and their families on March 20 at 12 PM ET. Russell Clayton, DO, Chief Medical Officer at Larimar, will be sharing updates about the nomlabofusp clinical program including information about opportunities for children, adolescents, and adults to enroll in the open label study as well as the upcoming phase 3 study. Register at https://ow.ly/gx8650YiY9n All reactions: 16 1 comment
Larimar’s Stock Soars After FDA Grants Breakthrough Therapy Designation News Platform Pricing Trading Guides Trading 101 Blog Level 2 Quotes Trading Terminology Stop Limit Orders Relative Volume Market Makers Guide Margin Rate Explainer Pivot Points beginner guides How to Day Trade for a Living What to Look for Before Investing Short Selling Day Trading Essentials How To Buy Stocks Stock Split Guide Psychology of Trading Technical Analysis Fundamental Analysis day trading Stocks to Watch AI Penny Stocks Day Trading Scanners Paper Trading Guide Low Float Stocks Pattern Trader Rule How to's How … fast-tracking, which aligns with Larimar’s strategy to file a Biologics License Application in 2026 and potentially launch the product by 2027. The stock’s price movement reflects this enthusiasm, indicating a strong marketu need for breakthrough treatments in rare diseases. Each news piece strengthens investor perspectives, focusing on long-term value accumulation despite current losses. Conclusion Larimar Therapeutics stands at a pivotal juncture, backed by FDA’s positive r … or as an endorsement, recommendation or sponsorship of any company, security or fund. StocksToTrade cannot and does not assess, verify or guarantee the adequacy, accuracy or completeness of any information, the suitability or profitability of any particular investment, or the potential value of any investment or informational source. The reader bears responsibility for his/her own investment research and decisions, should seek the advice of a qualified securities professional … list. Frequency of text messages may vary; reply STOP to opt-out. Normal rates apply and consent is not a condition of purchase as you can always receive info by calling us directly. This website may record your interactions with it and future calls may be recorded/monitored. I agree, Submit
EX-99.1 2 d917825dex991.htm EX-99.1 EX-99.1 Exhibit 99.1 Larimar Therapeutics Reports Second Quarter 2020 Operating and Financial Results • Merger between Chondrial Therapeutics and Zafgen completed and company began operating as Larimar Therapeutics • Phase 1 clinical trial of CTI-1601 for treatment of Friedreich’s ataxia restarts after delay due to COVID-19 related restrictions • $80 million private placement financing completed with biotechnology-focused institutional investors  … bsp; In July 2020, the EMA COMP issued a positive opinion on the company’s application for orphan drug designation for CTI-1601. Larimar expects that the European Commission, based on this positive opinion of the COMP, will formally grant the orphan drug designation for the European Union this year. Second Quarter 2020 Financial Results As of June 30, 2020, the Company had cash, cash equivalents, and marketable debt securities totaling $113.7 million. The Compa … 01 and future product candidates; the fact that the European Commission may not grant Orphan Drug Designation for the EU for CTI-1601 in FA or may do so in a longer than anticipated timeframe; Larimar’s ability to develop sales and marketing capabilities, whether alone or with potential future collaborators, and successfully commercialize any approved product candidates; Larimar’s ability to raise the necessary capital to conduct its product development activities;
Larimar City, in Punta Cana, is a... - Larimar City & Resort Facebook Log In Larimar City & Resort's Post Larimar City & Resort Verified account May 11 · Shared with Public Larimar City, in Punta Cana, is a resort city designed for year-round Caribbean living. The life you've always dreamed of is within reach. portal.larimarcity.com Your new lifestyle awaits in the Caribbean See details All reactions: 5 Like Comment
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About | Larimar Logistics Home About Contact Bridging the Benefits of the Dominican Republic to the World JOLIET, ILLINOIS United States Facility 90,000 sq. ft. Domestic Fulfillment, Returns, and Last Touch Embellishment SANTIAGO, DOMINICAN REPUBLIC Main Headquarters Zona Franca Gurabo 500,000+ sq. ft. Duty-Free Fulfillment, Last Touch Embellishment, Assembly, and Production Benefits of the Dominican Republic Modern Port Facilities Efficient and well-equipped ports facilitate smooth import and export processes, reducing lead times Robust Transportation Network An extensive and reliable transpo
Our Partners – Larimar Therapeutics --> Skip to content Toggle navigation About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Careers Our Science Scientific Approach Publications Our Programs Pipeline Nomlabofusp Expanded Access Policy Our Partners Investors Investors Press Releases Events & Presentations Corporate Governance Financials & Filings Stock Information Analyst Coverage Investor FAQS Contact Us Email Alerts News Contact Contact Us Directions About Larimar Company Overview Leadership Board of Directors Scientific Advisory Board Caree
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DEFM14A 1 d853876ddefm14a.htm DEFM14A DEFM14A Table of Contents UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 SCHEDULE 14A Proxy Statement Pursuant to Section 14(a) of the Securities Exchange Act of 1934 Filed by the Registrant ☒ Filed by a Party other than the Registrant ☐ Check the appropriate box: ☐ Prelim … to as the “ NASDAQ rules ”) (referred to as the “ share issuance proposal ” or “ Proposal 1 ”); 2. To approve an amendment to Zafgen’s ninth amended and restated certificate of incorporation to effect a reverse stock split of Zafgen common stock (referred to as the “ reverse stock split proposal ” or “ Proposal 2 ”); 3. To approve, on an advisory, non-binding, basis, the specified compensation … nection with the merger (referred to as the “ advisory merger compensation proposal ” or “ Proposal 3 ”); 4. To elect Jeffrey S. Hatfield, John L. LaMattina, Ph. D. and Frank E. Thomas as Class III directors of the Zafgen Board, to serve until Zafgen’s 2023 annual meeting of stockholders and until their successors are duly executed and qualified, subject to their earlier death, resignation or removal; provided, however, that, if the … ill be reconstituted as provided in the merger agreement (referred to as “ Proposal 4 ”); 5. To approve, on an advisory, non-binding, basis, the compensation paid to Zafgen’s named executive officers in 2019 (referred to as “ Proposal 5 ”); 6. To conduct an advisory, non-binding vote on the frequency of future advisory votes on executive compensation (referred to as “ Proposal 6 ”); 7. To ratify the … g firm for the fiscal year ending December 31, 2020 (referred to as “ Proposal 7 ”); and 8. To consider and vote upon an adjournment of the annual meeting, if necessary, to solicit additional proxies if there are not sufficient votes in favor of Proposals 1 and/or 2 (referred to as “ Proposal 8 ”). If Zafgen
Larimar Therapeutics | Life Sciences PA Close Who We Are About Us Meet Our Team Board of Directors Membership Membership Benefits Become a Member Member Directory Member News Advocacy The Voice for PA’s Life Sciences Policy Priorities Our Partners Action Center Life Sciences Events Events Calendar Overview of Events Submit Your Event to LSPA Sponsorship & Volunteer Opportunities Life Sciences Future 2026 Photo Gallery Podcast Resources Economic Impact Annual Report Purchasing & Savings Life Sciences Center Quarterly Newsletters Member Login Industry News Contact Us Who We Are About U … Partners Action Center Life Sciences Events Events Calendar Overview of Events Submit Your Event to LSPA Sponsorship & Volunteer Opportunities Life Sciences Future 2026 Photo Gallery Podcast Resources Economic Impact Annual Report Purchasing & Savings Life Sciences Center Quarterly Newsletters Larimar Therapeutics Back to Search Larimar Therapeutics Categories Biotechnology https://larimartx.com/ About Chondrial Therapeutics, LLC was formed to discover and develop … they need to succeed. $ Life Sciences Events Events Calendar Overview of Events Submit Your Event Sponsorship & Volunteer Opportunities Life Sciences Future Photo Gallery The Voice for PA's Life Sciences Through public policy advocacy in Harrisburg and Washington, D.C., Life Sciences PA serves as the voice for more than 960 member organizations across Pennsylvania that are critical to improving patient care, improving health globally, and to the economic growth of the Com
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