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Alexion Pharmaceuticals

Initiate Phase 3 trials of ULTOMIRIS in HSCT-TMA

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
30 Jan 2020
Due
31 Dec 2020
Delivered
December 2020
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“followed by Phase 3 trials in the second half of 2020, pending regulatory feedback.”

What we found

Evidence strength A What the grades mean

Alexion initiated a Phase III study of ULTOMIRIS (ALXN1210) in HSCT-TMA in December 2020, meeting the commitment to initiate the trial in the second half of 2020.

  • A
    Alexion Pharmaceuticals 10-K filed 2021-02-08 Regulatory filing · published 8 Feb 2021 · retrieved 21 Oct 2026 · kept permanently by the SEC · fingerprint 10caf5605550
    “In December 2020, Alexion initiated a Phase III, multicenter study to evaluate the safety and efficacy of ALXN1210 in HSCT-TMA.” ✓ confirmed on the page

Checked 21 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.

  • 3 versions
  1. Version 1 · original · stated 30 Jan 2020

    Deadline 31 Dec 2020 (“in the second half of 2020”)

  2. Version 2 · stated 30 Jul 2020

    Deadline 31 Dec 2021 (“in 2021”)

    “followed by Phase 3 trials in 2021, pending regulatory feedback.”

    Source for this version

  3. Version 3 · stated 29 Oct 2020

    Deadline 31 Dec 2020 (“by the end of 2020”) · wording expected

    “Alexion has initiated a Phase 3 study of ULTOMIRIS in adults with HSCT-TMA and plans to initiate a Phase 3 study in children with HSCT-TMA by the end of 2020.”

    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 milestone
Indicative materiality
Medium rules
Action
Initiate
Deliverable
Phase 3 trials of ULTOMIRIS in HSCT-TMA
In the company’s control
Medium
Specificity
High
Conditional
Yes: pending regulatory feedback
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-2020-C899866-019367 · Corrections policy

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