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Larimar Therapeutics, Inc.

Report top-line data from the Phase 2 trial

Delivered after the deadline

AI-confirmed · human review in progress Independent AI checks agreed on primary SEC or regulator evidence. Records are now being reviewed by hand, starting with those our customers order.

Announced
14 Sep 2022
Due
31 Dec 2023
Delivered
February 2024
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“with top-line data expected in 2H 2023”

What we found

Evidence strength A What the grades mean

The company reported preliminary data for a single cohort in May 2023, but the full top-line data for the completed Phase 2 dose exploration study was not reported until February 2024.

  • A
    Larimar Therapeutics, Inc. 10-K filed 2024-03-14 Regulatory filing · published 14 Mar 2024 · retrieved 1 Oct 2026 · kept permanently by the SEC · fingerprint cbbf912f4256
    “In May 2023, we reported preliminary unblinded top-line data from the 25 mg cohort of our Phase 2 four-week, placebo-controlled, dose exploration trial” ✓ confirmed on the page
  • A
    Larimar Therapeutics, Inc. 10-K filed 2024-03-14 Regulatory filing · published 14 Mar 2024 · retrieved 1 Oct 2026 · kept permanently by the SEC · fingerprint cbbf912f4256
    “In February 2024, we reported positive top-line data and successful completion of our four-week, placebo-controlled Phase 2 dose exploration study” ✓ confirmed on the page

Market reaction: the shares moved -9.9% against the S&P 500 over the three sessions around the disclosure (13 Mar 2024 to 18 Mar 2024). What this measures

Checked 1 Oct 2026.

Commitment lineage

Every time the company restated this commitment. The original is never changed, and the outcome is always measured against version 1.

  • Deadline drift +91 days
  • 3 versions
  1. Version 1 · original · stated 14 Sep 2022

    Deadline 31 Dec 2023 (“in 2H 2023”) · wording expected

  2. Version 2 · stated 25 Jul 2023

    Deadline 30 Jun 2024 (“in 1H 2024”) · wording expected

    “Top-line safety, pharmacokinetic, and pharmacodynamic (frataxin level) data from Phase 2 trial’s 50 mg cohort expected in 1H 2024”

    Source for this version

  3. Version 3 · stated 14 Nov 2023

    Deadline 31 Mar 2024 (“in Q1 2024”) · wording expected

    “Top-line safety, pharmacokinetic, and frataxin data from the Phase 2 trial now expected in Q1 2024”

    Source for this version

Commitment DNA

The structured record of this commitment. Fields the company did not state are left blank rather than guessed.

Event type
Clinical readout
Indicative materiality
Medium rules
Action
Report
Deliverable
top-line data from Phase 2 trial
Language
Expected (“expects”, “plans”)
In the company’s control
Medium
Specificity
Medium

How this entry was checked

  1. Commitment recordedThe company's words were matched word for word against the filing.
  2. First checkAn AI model, Gemini (Google), read the company's later filings and recorded the outcome with a quoted passage.
  3. Second check: disagreesClaude (Anthropic) re-read the evidence blind and read it as “Met”.
  4. Tie-breakA stronger model read the evidence and both earlier answers, without knowing which was recorded, and agrees with the recorded outcome.

Confirmed. This outcome counts towards the company's Kept Score. How verification works

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Report an error in this entry Reference: KI-C-2022-LRMR-002938 · Corrections policy

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