Study identifier:D702BC00001
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:2024-514281-39-00
A Phase III, Randomized, Double-blind, Multicenter, Global Study of Rilvegostomig or Pembrolizumab in Combination with Platinum-based Chemotherapy for the First-line Treatment of Patients with Metastatic Squamous Non-small Cell Lung Cancer Whose Tumors Express PD-L1 (ARTEMIDE-Lung02)
Non-small Cell Lung Cancer
Phase 3
No
Rilvegostomig, Pembrolizumab, Carboplatin, Paclitaxel, Nab-paclitaxel
All
880
Interventional
18 Years - n/a
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Oct 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Arm A Rilvegostomig in combination with carboplatin and paclitaxel or nab-paclitaxel followed by rilvegostomig | Drug: Rilvegostomig Administered intravenously (IV) on Day 1 of each 21-day cycle Other Name: AZD2936 Drug: Carboplatin Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Other Name: Not applicable Drug: Paclitaxel Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Other Name: Not applicable Drug: Nab-paclitaxel Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles Other Name: Not applicable |
Active Comparator: Arm B Pembrolizumab in combination with carboplatin and paclitaxel or nab-paclitaxel followed by pembrolizumab | Drug: Pembrolizumab Administered intravenously (IV) on Day 1 of each 21-day cycle Other Name: Keytruda Drug: Carboplatin Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Other Name: Not applicable Drug: Paclitaxel Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles Other Name: Not applicable Drug: Nab-paclitaxel Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles Other Name: Not applicable |