drugset / Trial / NCT03809624
Study of INBRX-105 and INBRX-105 With Pembrolizumab in Patients With Solid Tumors Including Head and Neck Cancer
Non-randomizedSequentialOpen-labelTreatment
Summary
This is a first-in-human, open-label, nonrandomized, four-part trial to determine the safety profile and identify the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of INBRX-105 and INBRX-105 in combination with Pembrolizumab. INBRX-105, a next generation bispecific antibody, targets the human programmed death-ligand 1 (PD-L1) receptor and the human 4-1BB receptor. INBRX-105 provides localized conditional T-cell co-stimulation through 4-1BB agonism.
Timeline
- Start
- 2019-01-30
- Primary completion
- 2024-10-03
- Completion
- 2024-10-03
Outcome
Outcome not reported
Stopped: “Program terminated due to lack of meaningful efficacy signal.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | INBRX-105 | Unknown | — | — |
| Subject | Pembrolizumab | Monoclonal antibody | 200 mg | Intravenous |