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A Phase I/2a Dose Escalation and Cohort Expansion Study of the Safety, Tolerability, and Efficacy of Anti-LAG-3 Monoclonal Antibody (BMS-986016) Administered Alone and in Combination With Anti-PD-1 Monoclonal Antibody (Nivolumab, BMS-936558) in Advanced Solid Tumors

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A Phase I/2a Dose Escalation and Cohort Expansion Study of the Safety, Tolerability, and Efficacy of Anti-LAG-3 Monoclonal Antibody (BMS-986016) Administered Alone and in Combination With Anti-PD-1 Monoclonal Antibody (Nivolumab, BMS-936558) in Advanced Solid Tumors

Status: Active, no longer recruiting
Phase of Trial: Phase I/II

Latest Information Update: 23 Jul 2024

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At a glance

  • Drugs Nivolumab (Primary) ; Nivolumab/relatlimab (Primary) ; Relatlimab (Primary)
  • Indications Bladder cancer; Carcinoma; Cervical cancer; Colorectal cancer; Gastric cancer; Head and neck cancer; Liver cancer; Malignant melanoma; Non-small cell lung cancer; Ovarian cancer; Renal cell carcinoma; Solid tumours; Squamous cell cancer
  • Focus Adverse reactions; Therapeutic Use
  • Acronyms RELATIVITY-020
  • Sponsors Bristol-Myers Squibb

    • Most Recent Events

    • 18 Jun 2024 Planned primary completion date changed from 22 May 2024 to 31 Oct 2024.
    • 21 May 2024 Planned End Date changed from 10 Sep 2025 to 31 Jan 2025.
    • 21 May 2024 Planned primary completion date changed from 10 Sep 2024 to 22 May 2024.

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