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uniQure N.V.

Disclose full safety and efficacy data from the first two cohorts

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
17 Dec 2021
Due
30 Jun 2023
Delivered
21 Jun 2023
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“Full safety and efficacy data from the first two cohorts in the Phase I/II clinical trial are expected in the first half of 2023”
  • SourceuniQure N.V. Form 8-K press release, 2021-12-17
  • FilingSEC filing index
  • Deadline as statedfirst half of 2023
  • Deadline used30 Jun 2023, the last day of the stated period
  • TypeProject
  • Permanent referenceKI-C-2021-QURE-001788
    Cite as https://keptindex.org/c/KI-C-2021-QURE-001788/ — this address never changes.

What we found

Evidence strength A What the grades mean

The company announced interim data from the Phase I/II clinical trial of AMT-130, including safety and efficacy information from the initial cohorts, on June 21, 2023, meeting the first-half 2023 deadline.

  • A
    uniQure N.V. 10-Q filed 2023-11-07 Regulatory filing · published 7 Nov 2023 · retrieved 1 Oct 2026 · kept permanently by the SEC
    “On June 21, 2023, we announced interim data, including up to 24-month follow-up, from 26 patients enrolled in the ongoing U.S. Phase I/II clinical trial of AMT-130.” ✓ confirmed on the page

Market reaction: the shares moved +2.7% against the S&P 500 over the three sessions around the disclosure (6 Nov 2023 to 9 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 readout
Indicative materiality
Medium rules
Action
Disclose
Deliverable
full safety and efficacy data
Where
United States
Language
Expected (“expects”, “plans”)
In the company’s control
Medium
Specificity
High
Conditional
Yes: after all patients in the higher-dose cohort have achieved one year of follow-up
Depends on
Customer, 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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