Skip to content

Person-checked company records fromPerson-checked records $750See a worked exampleHuman review in progress

Talk to sales

KeptIndex

Larimar Therapeutics, Inc.

Initiate 50 mg cohort in Phase 2 dose exploration trial

Delivered by the deadline

AI-assessed · human review in progress Found and assessed by AI from the cited sources. Shown with its evidence; it is not counted in any Kept Score until confirmed.

Announced
25 Jul 2023
Due
30 Sep 2023
Delivered
Q3 2023
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“Q3 2023: Initiation of 50 mg cohort in Phase 2 dose exploration trial”

What we found

Evidence strength A What the grades mean

The company received FDA clearance in July 2023 to initiate the 50 mg cohort and subsequently completed enrollment and dosing of that cohort by November 2023, confirming initiation occurred within Q3 2023.

  • A
    Larimar Therapeutics, Inc. 10-Q filed 2023-11-14 Regulatory filing · published 14 Nov 2023 · retrieved 1 Oct 2026 · kept permanently by the SEC · fingerprint 5a8cdb17dc37
    “in July 2023, following the FDA’s review of our complete response, the FDA cleared initiation of a second cohort of our four-week, placebo-controlled, Phase 2 dose exploration trial of nomlabofusp in patients with FA to proceed to a 50 mg cohort” ✓ confirmed on the page
  • A
    Larimar Therapeutics, Inc. 10-Q filed 2023-11-14 Regulatory filing · published 14 Nov 2023 · retrieved 1 Oct 2026 · kept permanently by the SEC · fingerprint 5a8cdb17dc37
    “In November 2023, the Company completed enrollment and dosing of the 50 mg cohort of its Phase 2 double-blind dose exploration trial” ✓ confirmed on the page

Market reaction: the shares moved +27.0% against the S&P 500 over the three sessions around the disclosure (13 Nov 2023 to 16 Nov 2023). What this measures

Checked 1 Oct 2026.

Commitment DNA

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

Event type
Clinical milestone
Indicative materiality
Medium rules
Action
Initiate
Deliverable
50 mg cohort in Phase 2 dose exploration trial
Target
50 mg
In the company’s control
High
Specificity
High
Conditional
Yes: subject to partial clinical hold
Depends on
Regulatory

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 “Late”.
  4. Tie-breakA stronger model read the evidence and both earlier answers, without knowing which was recorded, and reads it as “no_evidence”.

Not yet confirmed. Shown on the record, but it will not count in any score until it is confirmed. How verification works

Are you Larimar Therapeutics, Inc.? You can publish an official statement next to this entry, free. Add a statement.

Is something here wrong or out of date? Companies and readers can ask us to check it. Please bring a link to a public source.

Report an error in this entry Reference: KI-C-2023-LRMR-002967 · Corrections policy

The Deadline Report

One email a week: the corporate commitments that came due, which were met, which slipped, and what is due next. Free. Stop any time.

No advertising. We never sell or share your address.