A Study to Evaluate the Safety, Pharmacokinetics, and Activity of RO7502175 as a Single Agent and in Combination With Atezolizumab in Participants With Locally Advanced or Metastatic Solid Tumors
Solid Tumor
Unknown Primary
18 Years and older, Male and Female
GO43860 (primary)
NCI-2022-08852
2021-006708-34
Summary
This is a first-in-human study to evaluate the safety, tolerability, pharmacokinetics
(PK), and anti-tumor activity of RO7502175 when administered as a single agent and in
combination with atezolizumab in adult participants with locally advanced or metastatic
solid tumors, including non-small-cell lung cancer (NSCLC), head and neck squamous cell
carcinoma (HNSCC), melanoma, triple-negative breast cancer (TNBC), esophageal cancer,
gastric cancer, cervical cancer, urothelial carcinoma (UC), clear cell renal cell
carcinoma (RCC) and hepatocellular carcinoma (HCC). Participants will be enrolled in 2
stages: dose escalation and dose expansion.
Eligibility
- Life expectancy at least 12 weeks
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Measurable disease according to Response Evaluation criteria in Solid Tumors (RECIST) Version 1.1
- Histologically confirmed locally advanced, recurrent, or metastatic incurable solid tumor malignancy
- Tumor Specimen availability
Treatment Sites in Georgia
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