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Aldeyra Therapeutics, Inc.

Resubmit the NDA for reproxalap

Delivered by 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
13 Feb 2024
Due
31 Dec 2024
Delivered
3 Oct 2024
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“Proposed clinical trial top-line results and potential NDA resubmission are expected in the second half of 2024”

What we found

Evidence strength A What the grades mean

The company successfully resubmitted the NDA for reproxalap on October 3, 2024, which falls within the second half of 2024.

  • A
    Aldeyra Therapeutics, Inc. 10-K filed 2025-02-28 Regulatory filing · published 28 Feb 2025 · retrieved 2 Oct 2026 · kept permanently by the SEC · fingerprint 98fadc3c40a3
    “On October 3, 2024, Aldeyra announced resubmission of the NDA (the Resubmitted NDA)” ✓ confirmed on the page

Market reaction: the shares moved -1.3% against the S&P 500 over the three sessions around the disclosure (27 Feb 2025 to 4 Mar 2025). What this measures

Checked 2 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 +181 days
  • 2 versions
  1. Version 1 · original · stated 13 Feb 2024

    Deadline 31 Dec 2024 (“second half of 2024”) · wording expected

  2. Version 2 · stated 3 Apr 2025

    Deadline 30 Jun 2025 (“mid-2025”) · wording expected

    “Contingent on positive results and FDA discussions, NDA resubmission is anticipated mid-2025.”

    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
Regulatory submission
Indicative materiality
High rules
Action
Resubmit
Deliverable
NDA resubmission for reproxalap
Language
Expected (“expects”, “plans”)
In the company’s control
Medium
Specificity
Medium
Conditional
Yes: pending clinical trial results; feedback from ongoing FDA discussions
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: agreesA different AI model, Claude (Anthropic), re-read the evidence without being told the outcome and reached the same answer.

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-2024-ALDX-003540 · Corrections policy

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