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A Study to Evaluate the Safety and Pharmacokinetics of the Intravenous Fixed-Dose Combination (IV FDC) of Tiragolumab and Atezolizumab in Participants With Locally Advanced, Recurrent or Metastatic Solid Tumors (SKYSCRAPER-11)

NCT05661578 PHASE2 COMPLETED

The purpose of this study is to assess the safety, pharmacokinetics, and immunogenicity of tiragolumab and atezolizumab intravenous fixed-dose combination (IV FDC) in participants with histologically confirmed PD-L1-selected solid tumors whose disease is locally advanced, recurrent, or metastatic and for whom an investigational agent in combination with an anti-PD-L1 antibody is considered an acceptable treatment option.

Details

Lead sponsorHoffmann-La Roche
PhasePHASE2
StatusCOMPLETED
Enrolment64
Start dateThu May 04 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionFri Dec 26 2025 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

Greece, Serbia, Taiwan, South Korea, China, Croatia, United States, Turkey (Türkiye), Spain