• Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • Settings
  • RSS Feeds
Quantisnow Logo
  • Live Feeds
    • Press Releases
    • Insider Trading
    • FDA Approvals
    • Analyst Ratings
    • Insider Trading
    • SEC filings
    • Market insights
  • Analyst Ratings
  • Alerts
  • Subscriptions
  • Settings
  • RSS Feeds
PublishGo to App
    Quantisnow Logo

    © 2025 quantisnow.com
    Democratizing insights since 2022

    Services
    Live news feedsRSS FeedsAlertsPublish with Us
    Company
    AboutQuantisnow PlusContactJobsAI superconnector for talent & startupsNEWLLM Arena
    Legal
    Terms of usePrivacy policyCookie policy

    SEC Form S-8 filed by Larimar Therapeutics Inc.

    3/24/25 5:20:36 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care
    Get the next $LRMR alert in real time by email
    S-8 1 d930722ds8.htm S-8 S-8

    As filed with the United States Securities and Exchange Commission on March 24, 2025

    Registration No. 333-   

     

     

     

    UNITED STATES

    SECURITIES AND EXCHANGE COMMISSION

    Washington, D.C. 20549

     

     

    FORM S-8

    REGISTRATION STATEMENT

    Under

    THE SECURITIES ACT OF 1933

     

     

    LARIMAR THERAPEUTICS, INC.

    (Exact name of registrant as specified in its charter)

     

     

     

    Delaware   20-3857670
    (State or other jurisdiction of
    incorporation or organization)
      (I.R.S. Employer
    Identification No.)

     

    Three Bala Plaza East, Suite 506

    Bala Cynwyd, Pennsylvania

      19004
    (Address of Principal Executive Offices)   (Zip Code)

    Larimar Therapeutics, Inc. 2020 Equity Incentive Plan

    (Full title of the plan)

    Carole S. Ben-Maimon, M.D.

    President and Chief Executive Officer

    Larimar Therapeutics, Inc.

    Three Bala Plaza East, Suite 506

    Bala Cynwyd, Pennsylvania 19004

    (Name and address of agent for service)

    (844) 511-9056

    (Telephone number, including area code, of agent for service)

     

     

    Copies to:

    Rachael M. Bushey, Esq.

    Jennifer L. Porter, Esq.

    Goodwin Procter LLP

    3025 John F Kennedy Blvd

    Philadelphia, PA 19104

    (445) 207-7805

     

     

    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 company” in Rule 12b-2 of the Exchange Act.

     

     

     

    Large accelerated filer   ☐    Accelerated filer   ☐
    Non-accelerated filer   ☒    Smaller reporting company   ☒
         Emerging growth company   ☐

    If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 7(a)(2)(B) of the Securities Act. ☐

     

     

     


    EXPLANATORY NOTE

    This Registration Statement is being filed for the purpose of registering an additional 2,552,603 shares of common stock, par value $0.001 per share (the “Common Stock”), of Larimar Therapeutics, Inc. (the “Registrant”) that were added to the shares authorized for issuance under the Larimar Therapeutics, Inc. 2020 Equity Incentive Plan (the “Plan”) as a result of the operation of an automatic annual increase provision included therein and for which a Registration Statement on Form S-8 relating to the same employee benefit plan is effective.

    The Registrant previously filed Registration Statements on Form S-8 (File Nos. 333-249287, 333-270535 and 333-277946) with the Securities and Exchange Commission (the “Commission”) to register 6,510,258 shares of Common Stock that were authorized for issuance under the Plan. Upon the effectiveness of this Registration Statement, an aggregate of 9,062,861 shares of Common Stock will be registered for issuance from time to time under the Plan. Pursuant to General Instruction E to Form S-8, the contents of the Registration Statements on Form S-8 (File Nos. 333-249287, 333-270535 and 333-277946) filed with the Commission on October 2, 2020, March 14, 2023 and March 14, 2024 are incorporated herein by reference except to the extent supplemented, amended or superseded by the information set forth herein. Only those items of Form S-8 containing new information not contained in the earlier registration statement are presented herein.

    PART II

    INFORMATION REQUIRED IN THE REGISTRATION STATEMENT

     

    Item 3.

    Incorporation of Documents by Reference.

    The following documents of the Registrant filed with the Commission are incorporated by reference in this Registration Statement as of their respective dates:

    (a) the Registrant’s Annual Report on Form 10-K for the year ended December 31, 2024, filed with the Commission on March 24, 2025;

    (b) the Registrant’s Current Reports on Form 8-K (in each case other than portions thereof furnished under Item 2.02 or Item 7.01 of Form 8-K and exhibits accompanying such reports related to such items) filed with the Commission on January 10, 2025, January  27, 2025 and March 24, 2025; and

    (c) the description of the Registrant’s Common Stock contained in the Registration Statement on Form 8-A filed with the Commission on June 18, 2014 (File No. 001-36510), together with any amendment thereto filed with the Commission for the purpose of updating such description.

    All documents subsequently filed by the Registrant with the Commission pursuant to Sections 13(a), 13(c), 14 and 15(d) of the Securities Exchange Act of 1934, as amended (other than information furnished under Item 2.02 or 7.01 of Form 8-K and exhibits furnished on such form that relate to such items unless such form expressly provides to the contrary) prior to the filing of a post-effective amendment which indicates that all securities offered hereby have been sold or which deregisters all securities then remaining unsold, shall be deemed to be incorporated by reference into this Registration Statement and to be a part hereof from the date of filing such documents.

    Any statement contained in a document incorporated or deemed to be incorporated by reference herein shall be deemed to be modified or superseded for purposes of this Registration Statement to the extent that a statement contained in any subsequently filed document that also is deemed to be incorporated by reference herein modifies or supersedes such statement.


    Item 8.

    Exhibits.

    The following documents are filed as exhibits to this Registration Statement:

     

    Exhibit
    Number

      

    Description of Exhibit

      3.1    Ninth Amended and Restated Certificate of Incorporation of Larimar Therapeutics, Inc. (incorporated herein by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K (File No. 001-36510) filed on June 24, 2014).
      3.2    Certificate of Amendment of Ninth Amended and Restated Certificate of Incorporation of Zafgen, Inc. related to the Reverse Stock Split, dated May 28, 2020 (incorporated herein by reference to Exhibit 3.1 to the Company’s Current Report on Form 8-K (File No. 001-36510) filed on June 2, 2020).
      3.3    Certificate of Amendment of Ninth Amended and Restated Certificate of Incorporation of Zafgen, Inc. related to the Name Change, dated May 28, 2020 (incorporated herein by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K (File No. 001-36510) filed on June 2, 2020).
      3.4    Certificate of Amendment of Ninth Amended and Restated Certificate of Incorporation of Larimar Therapeutics, Inc., dated May  31, 2024 (incorporated herein by reference to Exhibit 3.1 to the Company’s Quarterly Report on Form 10-Q (File No. 001-36510) filed on August 8, 2024).
      3.5    Amended and Restated Bylaws of Larimar Therapeutics, Inc. (incorporated herein by reference to Exhibit 3.2 to the Company’s Current Report on Form 8-K (File No. 001-36510) filed on June 24, 2014).
      5.1*    Opinion of Goodwin Procter LLP.
     23.1*    Consent of PricewaterhouseCoopers LLP, independent registered public accounting firm for Larimar Therapeutics, Inc.
     23.2*    Consent of Goodwin Procter LLP (contained in Exhibit 5.1).
     24.1*    Power of Attorney (included on the signature page of this Registration Statement).
     99.1#    Larimar Therapeutics, Inc. 2020 Equity Incentive Plan (incorporated herein by reference to Exhibit 10.1 to the Company’s Current Report on Form 8-K/A (File No. 001-36510) filed on September 29, 2020).
     99.2#    Form of Stock Option Grant Notice and Award Agreement (incorporated herein by reference to Exhibit 10.2 to the Company’s Current Report on Form 8-K/A (File No. 001-36510) filed on September 29, 2020).
     99.3#    Form of Restricted Stock Unit Award Agreement (incorporated herein by reference to Exhibit 10.3 to the Company’s Annual Report on Form 10-K (File No. 001-36510) filed on March 14, 2024).
     99.4#    Form of Performance-Based Restricted Stock Unit Award Agreement (incorporated herein by reference to Exhibit  10.1 to the Company’s Current Report on Form 8-K (File No. 001-36510) filed on January 27, 2025).
    107*    Filing Fee Table.

     

    *

    Filed herewith

    #

    Denotes management contract or compensatory plan or arrangement.


    SIGNATURES

    Pursuant to the requirements of the Securities Act of 1933, the Registrant certifies that it has reasonable grounds to believe that it meets all of the requirements for filing on Form S-8 and has duly caused this Registration Statement to be signed on its behalf by the undersigned, thereunto duly authorized, in Bala Cynwyd, Commonwealth of Pennsylvania, on March 24, 2025.

     

    LARIMAR THERAPEUTICS, INC.

    By:   /s/ Carole S. Ben-Maimon, M.D.
      Carole S. Ben-Maimon, M.D.
      President and Chief Executive Officer

    POWER OF ATTORNEY

    KNOW ALL PERSONS BY THESE PRESENTS, that each person whose signature appears below hereby constitutes and appoints each of Carole S. Ben-Maimon, M.D. and Michael Celano as his or her true and lawful attorney-in-fact and agent with full power of substitution, for him or her in any and all capacities, to sign any and all amendments to this Registration Statement (including post-effective amendments thereto), and to file the same, with all exhibits thereto and other documents in connection therewith, with the Securities and Exchange Commission, granting unto said attorney-in-fact, proxy, and agent full power and authority to do and perform each and every act and thing requisite and necessary to be done in connection therewith, as fully for all intents and purposes as he or she might or could do in person, hereby ratifying and confirming all that said attorney-in-fact, proxy and agent, or his substitute, may lawfully do or cause to be done by virtue hereof.

    Pursuant to the requirements of the Securities Act of 1933, this Registration Statement has been signed by the following persons in the capacities and on the date indicated.

     

    Signature

      

    Title

     

    Date

    /s/ Carole S. Ben-Maimon, M.D.

    Carole S. Ben-Maimon, M.D.

      

    President, Chief Executive Officer and Director

    (Principal Executive Officer)

      March 24, 2025

    /s/ Michael Celano

    Michael Celano

      

    Chief Financial Officer

    (Principal Financial Officer and Principal Accounting Officer)

      March 24, 2025

    /s/ Joseph Truitt

    Joseph Truitt

       Chairman, Board of Directors   March 24, 2025

    /s/ Thomas E. Hamilton

    Thomas E. Hamilton

       Director   March 24, 2025

    /s/ Jonathan Leff

    Jonathan Leff

       Director   March 24, 2025

    /s/ Jeffrey W. Sherman, M.D., FACP

    Jeffrey W. Sherman, M.D., FACP

       Director   March 24, 2025

    /s/ Frank Thomas

    Frank Thomas

       Director   March 24, 2025
    Get the next $LRMR alert in real time by email

    Crush Q1 2026 with the Best AI Superconnector

    Stay ahead of the competition with Standout.work - your AI-powered talent-to-startup matching platform.

    AI-Powered Inbox
    Context-aware email replies
    Strategic Decision Support
    Get Started with Standout.work

    Recent Analyst Ratings for
    $LRMR

    DatePrice TargetRatingAnalyst
    1/29/2025$18.00Buy
    Truist
    10/16/2024$26.00Outperform
    Oppenheimer
    10/3/2024$22.00Outperform
    Wedbush
    10/2/2024$15.00Buy
    H.C. Wainwright
    9/4/2024$16.00Outperform
    Robert W. Baird
    4/3/2024$25.00Outperform
    Leerink Partners
    11/17/2023$4.50Neutral → Buy
    Citigroup
    10/19/2022$12.00Buy
    Guggenheim
    More analyst ratings

    $LRMR
    Insider Trading

    Insider transactions reveal critical sentiment about the company from key stakeholders. See them live in this feed.

    View All

    * Director by Deputization Flynn James E bought $30,000,000 worth of shares (9,375,000 units at $3.20) (SEC Form 4)

    4 - Larimar Therapeutics, Inc. (0001374690) (Issuer)

    8/4/25 6:28:33 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 4 filed by * Director by Deputization Flynn James E

    4 - Larimar Therapeutics, Inc. (0001374690) (Issuer)

    5/15/25 7:44:19 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 4 filed by Director Sherman Jeffrey W

    4 - Larimar Therapeutics, Inc. (0001374690) (Issuer)

    5/14/25 4:34:08 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $LRMR
    Press Releases

    Fastest customizable press release news feed in the world

    View All

    Larimar Therapeutics Reports Third Quarter 2025 Financial Results

    In the open label (OL) study, after 6-months of daily nomlabofusp administration, 100% of participants (n = 10) achieved skin FXN levels similar to asymptomatic carriersConsistent directional improvement across mFARS, FARS-ADL, 9-HPT and MFIS after 1-year in OL study reinforces the potential of nomlabofusp to alter FA's disease course relative to a worsening in a FACOMS natural history study reference populationOf 39 participants in OL study (and of 65 total participants who received at least 1 dose in all nomlabofusp studies), 7 experienced anaphylaxis in the first 6 weeks of dosing and returned to usual state of health after standard treatment; excluding these events, long term dosing of n

    11/5/25 7:00:00 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Larimar Therapeutics Announces Positive Data from Ongoing Long-term Open Label Study and Updates to Nomlabofusp Program for Friedreich's Ataxia

    In 4 completed studies and the ongoing OL study, 65 participants received at least 1 dose of nomlabofusp, including 39 in the OL study, with 14 on treatment for at least 6 months and 8 for over 1 year in the OL studyIncreases in skin FXN levels with short- and long-term daily nomlabofusp; 10/10 participants with data at 6 months achieved skin FXN levels over 50% of median levels in healthy volunteers (which is similar to levels in asymptomatic carriers)Consistent directional improvement across 4 key clinical outcomes (mFARS, FARS-ADL, 9-HPT, MFIS) observed after 1 year of nomlabofusp treatment could suggest potential for clinical benefit relative to a worsening in a FACOMS natural history st

    9/29/25 7:00:00 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Larimar Therapeutics Announces Conference Call on the Nomlabofusp Program for the Treatment of Friedreich's Ataxia

    BALA CYNWYD, Pa., Sept. 28, 2025 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (Larimar) (NASDAQ: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced that the Company will host a conference call and webcast to discuss updates for the Company's nomlabofusp clinical development program including data from the ongoing long-term open label study for the treatment of Friedreich's ataxia on Monday, September 29, 2025 at 8:00 am EDT. Conference Call and Webcast DetailsTo access the webcast on Monday, September 29, 2025 at 8:00 am EDT, please visit this link to the event. To participate by phone, please dial 1-877-407-9716 (do

    9/28/25 5:00:00 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $LRMR
    SEC Filings

    View All

    Larimar Therapeutics Inc. filed SEC Form 8-K: Other Events, Financial Statements and Exhibits

    8-K - Larimar Therapeutics, Inc. (0001374690) (Filer)

    11/10/25 7:01:20 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Amendment: SEC Form SCHEDULE 13G/A filed by Larimar Therapeutics Inc.

    SCHEDULE 13G/A - Larimar Therapeutics, Inc. (0001374690) (Subject)

    11/6/25 4:17:54 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    SEC Form 10-Q filed by Larimar Therapeutics Inc.

    10-Q - Larimar Therapeutics, Inc. (0001374690) (Filer)

    11/5/25 4:15:37 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $LRMR
    Insider Purchases

    Insider purchases reveal critical bullish sentiment about the company from key stakeholders. See them live in this feed.

    View All

    $LRMR
    Analyst Ratings

    Analyst ratings in real time. Analyst ratings have a very high impact on the underlying stock. See them live in this feed.

    View All

    * Director by Deputization Flynn James E bought $30,000,000 worth of shares (9,375,000 units at $3.20) (SEC Form 4)

    4 - Larimar Therapeutics, Inc. (0001374690) (Issuer)

    8/4/25 6:28:33 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Hamilton Thomas Edward bought $499,998 worth of shares (57,208 units at $8.74), increasing direct ownership by 11% to 564,798 units (SEC Form 4)

    4 - Larimar Therapeutics, Inc. (0001374690) (Issuer)

    5/31/24 4:56:58 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Flynn James E bought $37,499,993 worth of shares (4,290,617 units at $8.74) (SEC Form 4)

    4 - Larimar Therapeutics, Inc. (0001374690) (Issuer)

    2/16/24 2:37:50 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Truist initiated coverage on Larimar Therapeutics with a new price target

    Truist initiated coverage of Larimar Therapeutics with a rating of Buy and set a new price target of $18.00

    1/29/25 7:39:50 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Oppenheimer initiated coverage on Larimar Therapeutics with a new price target

    Oppenheimer initiated coverage of Larimar Therapeutics with a rating of Outperform and set a new price target of $26.00

    10/16/24 7:29:15 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Wedbush initiated coverage on Larimar Therapeutics with a new price target

    Wedbush initiated coverage of Larimar Therapeutics with a rating of Outperform and set a new price target of $22.00

    10/3/24 7:34:56 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $LRMR
    Financials

    Live finance-specific insights

    View All

    Larimar Therapeutics Announces Positive Data from Ongoing Long-term Open Label Study and Updates to Nomlabofusp Program for Friedreich's Ataxia

    In 4 completed studies and the ongoing OL study, 65 participants received at least 1 dose of nomlabofusp, including 39 in the OL study, with 14 on treatment for at least 6 months and 8 for over 1 year in the OL studyIncreases in skin FXN levels with short- and long-term daily nomlabofusp; 10/10 participants with data at 6 months achieved skin FXN levels over 50% of median levels in healthy volunteers (which is similar to levels in asymptomatic carriers)Consistent directional improvement across 4 key clinical outcomes (mFARS, FARS-ADL, 9-HPT, MFIS) observed after 1 year of nomlabofusp treatment could suggest potential for clinical benefit relative to a worsening in a FACOMS natural history st

    9/29/25 7:00:00 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Larimar Therapeutics Announces Conference Call on the Nomlabofusp Program for the Treatment of Friedreich's Ataxia

    BALA CYNWYD, Pa., Sept. 28, 2025 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. (Larimar) (NASDAQ: LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced that the Company will host a conference call and webcast to discuss updates for the Company's nomlabofusp clinical development program including data from the ongoing long-term open label study for the treatment of Friedreich's ataxia on Monday, September 29, 2025 at 8:00 am EDT. Conference Call and Webcast DetailsTo access the webcast on Monday, September 29, 2025 at 8:00 am EDT, please visit this link to the event. To participate by phone, please dial 1-877-407-9716 (do

    9/28/25 5:00:00 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Larimar Therapeutics Announces FDA Recommendations on Safety Database, and Other Details of Nomlabofusp BLA Submission for Friedreich's Ataxia Program

    Interactions with FDA over the past year have provided clear expectations for the path to submission of the nomlabofusp BLAWritten FDA recommendations for safety database include a total of at least 30 participants with continuous exposure for 6 months including a subset of at least 10 with 1-year; large majority of the exposure should be on the 50 mg dose BLA submission seeking accelerated approval planned in the second quarter of 2026 to allow for inclusion of the recommended safety data for adults and childrenOLE data expected in September 2025 from 30-40 participants who received at least one dose of nomlabofusp; data will include participants on the 50 mg doseAdolescent PK run-in data e

    6/23/25 7:00:00 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $LRMR
    Large Ownership Changes

    This live feed shows all institutional transactions in real time.

    View All

    Amendment: SEC Form SC 13G/A filed by Larimar Therapeutics Inc.

    SC 13G/A - Larimar Therapeutics, Inc. (0001374690) (Subject)

    11/14/24 5:05:19 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Amendment: SEC Form SC 13G/A filed by Larimar Therapeutics Inc.

    SC 13G/A - Larimar Therapeutics, Inc. (0001374690) (Subject)

    11/14/24 11:41:09 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Amendment: SEC Form SC 13G/A filed by Larimar Therapeutics Inc.

    SC 13G/A - Larimar Therapeutics, Inc. (0001374690) (Subject)

    11/14/24 9:16:35 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    $LRMR
    Leadership Updates

    Live Leadership Updates

    View All

    Larimar Therapeutics Appoints Dr. Jeffery W. Sherman to its Board of Directors

    BALA CYNWYD, Pa., Oct. 03, 2023 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. ("Larimar") (NASDAQ:LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced the appointment of Jeffrey W. Sherman, M.D., F.A.C.P. to the Company's Board of Directors, effective today. Dr. Sherman, currently Executive Vice President, Chief Medical Officer (CMO) at Horizon Therapeutics Public Limited Company, has over 20 years of executive experience in regulatory and clinical strategy. "Dr. Sherman is a pharmaceutical industry veteran who brings decades of leadership experience in global regulatory and clinical strategy to our Board of Directors.

    10/3/23 4:05:00 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Larimar Therapeutics Reports Second Quarter 2023 Operating and Financial Results

    Initiation cleared for 50 mg cohort in Phase 2 Friedreich's ataxia (FA) dose exploration trial following FDA review of unblinded 25 mg cohort Phase 2 dataInitiation cleared for open-label extension (OLE) trial following FDA review of unblinded 25 mg cohort Phase 2 dataTop-line safety, pharmacokinetic, and frataxin data from the Phase 2 trial's 50 mg cohort expected in 1H 2024Initiation of OLE trial with 25 mg daily dosing expected in Q1 2024; interim data expected in Q4 2024 Cash, cash equivalents and marketable securities of $104.2 million as of June 30, 2023, provides projected cash runway into Q4 2024 BALA CYNWYD, Pa., Aug. 10, 2023 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. ("Lari

    8/10/23 7:00:00 AM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care

    Larimar Therapeutics Appoints Dr. Rusty Clayton as Chief Medical Officer

    BALA CYNWYD, Pa., July 17, 2023 (GLOBE NEWSWIRE) -- Larimar Therapeutics, Inc. ("Larimar") (NASDAQ:LRMR), a clinical-stage biotechnology company focused on developing treatments for complex rare diseases, today announced the appointment of Russell "Rusty" Clayton, DO, as Chief Medical Officer ("CMO"), effective today. Dr. Clayton succeeds former CMO Nancy M. Ruiz, MD, who is retiring and will provide consulting support to the Company as needed. "We are delighted to welcome Dr. Clayton in his new role as CMO as we further expand our clinical development of CTI-1601. Rusty has been one of our closest advisors for the last 5 years, has attended every meeting between Larimar and the FDA, in

    7/17/23 4:05:00 PM ET
    $LRMR
    Biotechnology: Pharmaceutical Preparations
    Health Care