LIGHTBEAM-U01 Substudy 01B: A Phase 1/2 Substudy to Evaluate the Safety and Efficacy of Pembrolizumab in Combination With Investigational Agents in Pediatric and Young Adult Participants With Hematologic Malignancies or Solid Tumors
Latest Information Update: 06 Mar 2025
At a glance
- Drugs Favezelimab (Primary) ; Favezelimab/pembrolizumab (Primary) ; Pembrolizumab (Primary) ; Pembrolizumab+vibostolimab (Primary) ; Vibostolimab (Primary)
- Indications Hodgkin's disease; Malignant melanoma; Solid tumours
- Focus Adverse reactions; Pharmacokinetics; Therapeutic Use
- Acronyms LIGHTBEAM-U01
- Sponsors Merck Sharp & Dohme
- 03 Mar 2025 Planned initiation date changed from 13 Dec 2024 to 15 Jan 2025.
- 16 Jan 2025 Status changed from recruiting to withdrawn prior to enrolment.
- 10 Dec 2024 Planned initiation date changed from 14 Nov 2024 to 13 Dec 2024.