A Study of Intismeran Autogene (V940)/Placebo + Pembrolizumab and Chemotherapy in Metastatic Squamous Non-Small Cell Lung Cancer (V940-013)
Part of paid clinical trials in Tampa, Florida.
- Sponsor
- Merck Sharp & Dohme LLC
- Study ID
- NCT07221474
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Squamous Non-small Cell Lung Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Intismeran Autogene — BIOLOGICAL1 mg Intramuscular (IM) Injection
- Pembrolizumab — BIOLOGICAL200 mg IV Infusion
- Carboplatin — DRUGArea Under the Curve (AUC) either 6 or 5 (mg/mL/min) IV Infusion
- Paclitaxel — DRUG200 or 175 mg/m\^2 IV Infusion
- Nab-paclitaxel — DRUG100 mg/m\^2 IV Infusion
- Placebo — OTHERPlacebo matched to Intismeran Autogene IM injection
Study Details
Researchers want to know if intismeran autogene (the study treatment) given with pembrolizumab and chemotherapy can treat metastatic treatment-naive squamous non-small cell lung cancer (NSCLC). Intismeran autogene is designed to help a person's immune system attack their specific cancer. The goal of this study is to learn if people who receive intismeran autogene with pembrolizumab and chemotherapy live longer overall and without the cancer growing or spreading compared to people who receive placebo with pembrolizumab and chemotherapy. A placebo looks like the study treatment but has no study treatment in it. Using a placebo helps researchers better understand the effects of the study treatment.
Key Dates
- First listed
- Oct 28, 2025
- Start date
- Dec 12, 2025
- Status verified
- Jul 2026
- Primary completion
- Jul 2, 2029
- Completion
- May 6, 2031
Study Design
- Enrollment
- 180 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Intismeran Autogene + Pembrolizumab + ChemoInduction phase: Participants receive pembrolizumab 400 mg intravenous (IV) infusion on Day 1 of a six week cycle plus a platinum doublet chemotherapy regimen (carboplatin area under the curve (AUC) 6 or 5 mg/mL/min IV infusion every 3 weeks (Q3W) × 2 doses combined either with paclitaxel 200 or 175 mg/m\^2 IV infusion Q3W × 2 doses, OR with nab paclitaxel 100 mg/m\^2 IV infusion weekly × 6 doses). Intismeran Autogene 1 mg intramuscular (IM) injection is administered on Days 1 and 22 of Cycle 2 Induction (Q3W) for up to 2 doses. Maintenance phase: Participants receive pembrolizumab 400 mg IV infusion on Day 1 every 6 weeks (Q6W) for up to 15 doses. Intismeran Autogene 1 mg IM injection is administered on Days 1 and 22 (Q3W) for up to 7 doses during maintenance.
- Experimental: Placebo + Pembrolizumab + ChemoInduction phase: Participants receive pembrolizumab 400 mg intravenous (IV) infusion on Day 1 of a six week cycle plus a platinum doublet chemotherapy regimen (carboplatin area under the curve (AUC) 6 or 5 mg/mL/min IV infusion every 3 weeks (Q3W) × 2 doses combined either with paclitaxel 200 or 175 mg/m\^2 IV infusion Q3W × 2 doses, OR with nab paclitaxel 100 mg/m\^2 IV infusion weekly × 6 doses). Placebo intramuscular (IM) injection is administered on Days 1 and 22 of Cycle 2 Induction (Q3W) for up to 2 doses. Maintenance phase: Participants receive pembrolizumab 400 mg IV infusion on Day 1 every 6 weeks (Q6W) for up to 15 doses. Placebo IM injection is administered on Days 1 and 22 (Q3W) for up to 7 doses during maintenance.
Primary Outcome Measure
Progression Free Survival (PFS) [ Time Frame: Up to ~32 months ]
Central Contacts
- Toll Free Number1-888-577-8839
Locations (10)
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