drugset / Trial / NCT04551352

A Study of RO7293583 in Participants With Unresectable Metastatic Tyrosinase Related Protein 1 (TYRP1)-Positive Melanomas

NCT04551352

Phase 1 Completed 20 enrolled Hoffmann-La Roche
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

EvaluationDrugModalityDoseRoute
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