Atezolizumab Plus Bevacizumab in First Line NSCLC Patients
- Sponsor
- Fundación GECP
- Study ID
- NCT03836066
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Atezolizumab-Bevacizumab — DRUGAtezoluzumab 1200 mg + Bevacizumab 15 mg / kg
Study Details
This is a multi-center phase II clinical trial of atezolizumab in combination with bevacizumab as first line treatment for locally advanced or metastasic high-intermediate tumour mutation burden selected NSCLC patients. 102 patients will be enrolled in this trial to examine the efficacy of this combination measured by progression free survival according to response evaluation Criteria in solid tumours (RECIST) version 1.1.
Key Dates
- Start date
- May 15, 2019
- Status verified
- Nov 2025
- Primary completion
- Oct 21, 2024
- Completion
- Oct 21, 2024
Study Design
- Enrollment
- 41 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Experimental: Atezolizumab plus Bevacizumab arm1 group, Atezolizumab 1200mb + Bevacizumab 15 mg/kg (IV),every 21 days.
Primary Outcome Measure
Efficacy of Atezolizumab in Combination With Bevacizumab - PFS [ Time Frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months ]
Related coverage on Hipa.ai
- Atezolizumab Plus Bevacizumab Shows 11.3-Month PFS in First-Line NSCLCAtezolizumab · Dec 4, 2025 · ClinicalTrials.gov
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