OPEN-LABEL, MULTICENTER, DOSE ESCALATION PHASE IB STUDY WITH EXPANSION PHASE TO EVALUATE THE SAFETY, PHARMACOKINETICS AND ACTIVITY OF RO5509554 AND MPDL3280A ADMINISTERED IN COMBINATION IN PATIENTS WITH ADVANCED SOLID TUMORS
Latest Information Update: 17 Apr 2025
At a glance
- Drugs Atezolizumab (Primary) ; Emactuzumab (Primary)
- Indications Advanced breast cancer; Bladder cancer; Gastric cancer; Ovarian cancer; Soft tissue sarcoma; Solid tumours
- Focus Adverse reactions
- Sponsors Roche
Most Recent Events
- 14 Apr 2025 According to SynOx Therapeutics media release, the United States Food and Drug Administration (FDA) has granted Fast Track Designation (FTD) to emactuzumab for the treatment of TGCT patients that are not amenable to or who would not benefit from surgery supported by data from Phase 1/2 clinical studies demonstrating rapid, robust tumour reduction and durable response combined with a manageable safety profile.
- 26 Aug 2020 Status changed from active, no longer recruiting to completed.
- 10 Jul 2020 Planned End Date changed from 29 May 2020 to 17 Jul 2020.