A Study to Compare Pharmacokinetics, Efficacy, Safety, and Immunogenicity of MB12 (Proposed Pembrolizumab Biosimilar) to Keytruda® in Non-small Cell Lung Cancer (BENITO Study)
Randomized, Multicenter, Multinational, Double-Blind Study to Compare the Pharmacokinetics, Efficacy, Safety and Immunogenicity of MB12 (Proposed Pembrolizumab Biosimilar) Versus Keytruda® in Combination With Chemotherapy for the Treatment of Patients With Advanced Stage IV Non-Squamous Non-Small Cell Lung Cancer (NSCLC) (BENITO Study)
About This Trial
This is a randomized, multicenter, multinational, double-blind, integrated pharmacokinetics (PK) and efficacy similarity study to compare the PK, efficacy, safety, and immunogenicity of MB12 versus Keytruda® in combination with pemetrexed-platinum chemotherapy as first-line treatment in patients with metastatic non-squamous NSCLC.
Who May Be Eligible (Plain English)
Original Eligibility Criteria
View original clinical language
Treatments Being Tested
MB12 (Proposed Pembrolizumab Biosimilar)
200mg IV, every 3 weeks on Day 1
EU-sourced Keytruda®
200mg IV, every 3 weeks on Day 1
US-sourced Keytruda®
200mg IV, every 3 weeks on Day 1
Pemetrexed
500 mg/m2 IV, every 3 weeks on Day 1
Carboplatin
Area under the curve (AUC) 5 IV, every 3 weeks on Day 1 for 4 cycles.
Cisplatin
75 mg/m2 IV, every 3 weeks on Day 1 for 4 cycles