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Bristol Myers Squibb Co.

Launch relatlimab plus nivolumab, mavacamten, and deucravacitinib

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
4 Feb 2022
Due
31 Dec 2022
Delivered
by 31 Dec 2022
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“I am confident in our ability to execute against our key milestones in 2022, including three planned first-in-class launches with relatlimab plus nivolumab fixed dose combination, mavacamten and deucravacitinib.”

What we found

Evidence strength A What the grades mean

Bristol Myers Squibb successfully launched all three first-in-class medicines—relatlimab plus nivolumab (Opdualag), mavacamten (Camzyos), and deucravacitinib (Sotyktu)—during 2022.

  • A
    Bristol Myers Squibb Co. 8-K filed 2023-02-02 Regulatory filing · published 2 Feb 2023 · retrieved 3 Oct 2026 · kept permanently by the SEC · fingerprint 301fe92f9810
    “We are especially proud to have launched three first-in-class medicines that address serious unmet medical needs for patients.” ✓ confirmed on the page
  • A
    Bristol Myers Squibb Co. 10-K filed 2023-02-14 Regulatory filing · published 14 Feb 2023 · retrieved 3 Oct 2026 · kept permanently by the SEC · fingerprint 6f682e608fa9
    “Camzyos (mavacamten)Obstructive HCMOctober 2022 Announced that the FDA accepted the supplemental NDA for Camzyos” ✓ confirmed on the page
  • A
    Bristol Myers Squibb Co. 10-Q filed 2023-04-27 Regulatory filing · published 27 Apr 2023 · retrieved 3 Oct 2026 · kept permanently by the SEC · fingerprint 724447c45b84
    “Opdualag was launched in March 2022.” ✓ confirmed on the page

Market reaction: the shares moved +4.9% against the S&P 500 over the three sessions around the disclosure (1 Feb 2023 to 6 Feb 2023). What this measures

Checked 3 Oct 2026.

Commitment DNA

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

Event type
Commercial launch
Indicative materiality
Medium rules
Action
Launch
Deliverable
relatlimab plus nivolumab, mavacamten, and deucravacitinib
Language
Expected (“expects”, “plans”)
In the company’s control
High
Specificity
High

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-2022-BMY-004353 · Corrections policy

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