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.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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