Stopped: Study termination was based on strategic considerations and not due to specific safety reasons or a request from a regulatory authority.
Open-label, multi-center, non-randomized, multiple dose, safety, tolerability, pharmacokinetic, and pharmacodynamics and clinical activity study of PF-06940434 (Integrin alpha-V/beta-8 Antagonist) in patients with SCCHN (Squamous Cell Carcinoma of the Head and Neck), renal cell carcinoma (RCC - clear cell and papillary), ovarian, gastric, esophageal, esophageal (adeno and squamous), lung squamous cell, pancreatic and biliary duct, endometrial, melanoma and urothelial tumors. This study contains two parts, single agent dose escalation (Part 1A), dose finding of PF 06940434 in combination with anti-PD-1 (Part 1B) and dose expansion (Part 2). Part 2 Dose Combination Expansion will enroll participants into 3 cohorts at doses determined from Part 1B in order to further evaluate the safety of PF-06940434 in combination with anti-PD-1.
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Number of participants with Dose-limiting toxicities (DLT) for Dose Escalation and Dose Finding
Timeframe: Baseline up to 28 Days (Cycle 1)
Number of Participants With Clinically Significant Change From Baseline in Laboratory Abnormalities
Timeframe: Baseline up to approximately 24 months
Number of Participants With Adverse Events (AEs) According to Severity
Timeframe: Baseline up to approximately 24 months
Number of Participants With Adverse Events (AEs) According to Seriousness
Timeframe: Baseline up to up to approximately 24 months
Number of Participants With Adverse Events (AEs) by Relationship
Timeframe: Baseline up to approximately 24 months
Progression-Free Survival (PFS) for Dose Expansion
Timeframe: Baseline up to 24 Months
Objective Response Rate - Percentage of Participants With Objective Response in Dose Expansion
Timeframe: Baseline up to 24 months
Duration of Response (DR) for Dose Expansion
Timeframe: Baseline up to 24 Months