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Unicycive Therapeutics, Inc.

File an Investigational Drug Application for a Phase 1 study of UNI-494

Not 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
14 Nov 2022
Due
31 Mar 2023
Checked
1 Oct 2026
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“Unicycive plans to file an Investigational Drug Application (IND) with the FDA in early 2023”

What we found

Evidence strength A What the grades mean

The company did not file an IND for a Phase 1 study of UNI-494 in early 2023, instead shifting its FDA IND filing plans to 2024 for a Phase 2 trial.

  • A
    Unicycive Therapeutics, Inc. 8-K filed 2023-03-31 Regulatory filing · published 31 Mar 2023 · retrieved 1 Oct 2026 · kept permanently by the SEC · fingerprint 917c54f8ce66
    “plans to file a corresponding Investigational New Drug (IND) application with the FDA in 2024 for a Phase 2 proof-of-concept trial” ✓ confirmed on the page

Market reaction: the shares moved +14.7% against the S&P 500 over the three sessions around the disclosure (30 Mar 2023 to 4 Apr 2023). 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 +641 days
  • 2 versions
  1. Version 1 · original · stated 14 Nov 2022

    Deadline 31 Mar 2023 (“in early 2023”) · wording expected

  2. Version 2 · stated 31 Mar 2023

    Deadline 31 Dec 2024 (“2024”) · wording expected

    “plans to file a corresponding Investigational New Drug (IND) application with the FDA in 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
Regulatory filing
Indicative materiality
Medium rules
Action
File
Deliverable
UNI-494 Investigational Drug Application
Language
Expected (“expects”, “plans”)
In the company’s control
High
Specificity
High
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.
  4. Third check on a negative finding: agreesBecause a negative finding could harm a company if wrong, a stronger model re-read the evidence fully blind 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-2022-UNCY-002779 · Corrections policy

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