CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 182 enrolled
Drug / intervention
Tobemstomig +4 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05775289
NCT05775289Phase 2Active

A Phase II, Randomized, Multicenter, Double-Blind, Controlled Study of Tobemstomig Plus Platinum-Based Chemotherapy Versus Pembrolizumab Plus Platinum-Based Chemotherapy in Patients With Previously Untreated Locally Advanced or Metastatic Non-Small Cell Lung Cancer

Hoffmann-La Roche·interventional·Posted Mar 20, 2023·Updated May 13, 2026

In Brief

A Phase 2 clinical trial evaluating Tobemstomig, Pembrolizumab, and 3 other interventions for Non-small Cell Lung Cancer. Active but no longer recruiting, targeting 182 participants across 50 sites in 11 countries.

Detailed Summary

The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics of tobemstomig (RO7247669) in combination with platinum-based chemotherapy compared with pembrolizumab plus platinum-based chemotherapy in participants with previously untreated, locally advanced, unresectable (Stage IIIB/IIIC) or metastatic (Stage IV) non-small-cell lung cancer (NSCLC) who are not eligible to receive curative surgery and/or definitive chemoradiotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Belgium, Brazil, France, Germany, Italy, Mexico, South Korea, Spain, Turkey (Türkiye), United States
Collaborators--

Timeline

Phase 2ActiveOverdue
202420252026
First PostedMar 20, 2023
Enrollment StartMar 15, 2023
Primary CompletionJun 20, 2024
Study CompletionJun 1, 2026
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 3.3 years ago

Interventions

Tobemstomigdrug

Participants will receive intravenous (IV) tobemstomig for four 21-day cycles

Pembrolizumabdrug

Participants will receive IV pembrolizumab four 21-day cycles

Paclitaxeldrug

Participants will receive IV paclitaxel Q3W for four 21-day cycles

Pemetrexeddrug

Participants will receive IV pemetrexed Q3W until disease progression or unacceptable toxicity

Carboplatindrug

Participants will receive IV carboplatin Q3W for four 21-day cycles