A Multicenter, Open-label, Phase 3 Study to Evaluate the Long-term Safety and Efficacy in Participants Who Are Currently on Treatment or in Follow-up in Studies That Include Pembrolizumab
Latest Information Update: 14 Mar 2025
At a glance
- Drugs Favezelimab (Primary) ; Lenvatinib (Primary) ; Olaparib (Primary) ; Pembrolizumab (Primary) ; Antineoplastics; Antineoplastics
- Indications Haematological malignancies; Solid tumours
- Focus Therapeutic Use
- Acronyms KEYNOTE-587; MK-3475-587/KEYNOTE-587
- Sponsors Merck Sharp & Dohme Corp.
- 26 Feb 2025 Study arms increased from 9 to 15. New drugs added to the study arms. Drugs olaparib and favezelimab added newly.
- 15 Sep 2024 According to a Merck AG Media Release, results of this study being presented at ESMO include an analysis of the efficacy and safety outcomes for 211 former KEYNOTE-006 participants who transitioned to KEYNOTE-587 (KEYTRUDA, n=159; ipilimumab, n=52) after 10 years of follow-up and an analysis of additional antitumor activity in patients who received a second course of KEYTRUDA.
- 21 Dec 2023 The given protocol has been amended as above- 1) Planned number of patients has been changed from 2300 to 3500. 2) Number of treatment arms has been changed from 5 to 9.