drugset / Trial / NCT04551352
A Study of RO7293583 in Participants With Unresectable Metastatic Tyrosinase Related Protein 1 (TYRP1)-Positive Melanomas
Non-randomizedSequentialOpen-labelTreatment
Summary
This is a first-in-human, multi-center clinical study to determine the safety, Maximum Tolerated Dose (MTD) and/or Optimal Biological Dose (OBD) as well as the optimal schedule for intravenous (IV) and/or subcutaneous (SC) administrations of RO7293583 with or without obinutuzumab pretreatment, in participants with unresectable metastatic TYRP1-positive melanomas who have progressed on standard of care (SOC) treatment, are intolerant to SOC, or are non-amenable to SOC. This study will include an initial single participant dose-escalation part one followed by a multiple participant dose-escalation part two with the possibility of expansion.
Timeline
- Start
- 2020-10-28
- Primary completion
- 2022-07-28
- Completion
- 2022-07-28
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RO7293583 | Unknown | 0.045 mg | Intravenous |
| Subject | RO7293583 | Unknown | 0.4 mg | Intravenous |
| Subject | RO7293583 | Unknown | 1.5 mg | Intravenous |
| Subject | RO7293583 | Unknown | 160 mg | Intravenous |
| Subject | RO7293583 | Unknown | 600 mg | Intravenous |
| Background | Adalimumab | Monoclonal antibody | — | — |
| Background | Obinutuzumab | Monoclonal antibody | — | — |
| Background | Tocilizumab | Monoclonal antibody | — | — |