A Phase 1b Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Bemarituzumab Monotherapy and Combination With Other Anti-Cancer Therapy in Subjects With Squamous-Cell Non-Small-Cell Lung Cancer (FORTITUDE-201)
Latest Information Update: 24 Jun 2024
At a glance
- Drugs Antineoplastics (Primary) ; Bemarituzumab (Primary) ; Carboplatin (Primary) ; Docetaxel (Primary) ; Paclitaxel (Primary) ; Pembrolizumab (Primary)
- Indications Non-small cell lung cancer; Squamous cell cancer
- Focus Adverse reactions
- Acronyms FORTITUDE-201
- Sponsors Amgen
- 18 Jun 2024 Status changed from active, no longer recruiting to completed.
- 08 May 2024 Planned End Date changed from 30 Apr 2024 to 31 May 2024.
- 31 Oct 2023 According to an Amgen media release, FORTITUDE-201, a Phase 1b study of bemarituzumab monotherapy and in combination with standard of care therapy, in squamous NSCLC with FGFR2b overexpression, will be discontinued.