A Phase 1 Study To Evaluate Escalating Doses Of A Vaccine-Based Immunotherapy Regimen For Prostate Cancer (PrCa VBIR)
Part of paid clinical trials in Tucson, Arizona.
- Sponsor
- Pfizer
- Study ID
- NCT02616185
- Phase
- PHASE1
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- PF-06755992 — BIOLOGICALPF-06755992 will be administered on Day 1 of Cycles 1 and 2.
- PF-06755990 — BIOLOGICALPF-06755990 will be administered using a device on Day 29, 57 and 85 of each cycle.
- TDS-IM Electroporation Device — DEVICETDS-IM electroporation device and associated supplies will be used for PF-06755990 administration
- Tremelimumab — BIOLOGICALPF-06753388 will be administered every 28 days.
- PF-06801591 — BIOLOGICALPF-06801591 will be administered every 28 days.
- PF-06753512 — BIOLOGICALCombination of adenovirus (AdC68) + plasmid DNA (pDNA) + tremelimumab
Study Details
The study will evaluate the safety, pharmacokinetics and pharmacodynamics of increasing doses of a vaccine-based immunotherapy regimen for patients with prostate cancer.
Key Dates
- Start date
- Dec 30, 2015
- Status verified
- Jan 2023
- Primary completion
- Feb 23, 2021
- Completion
- Feb 23, 2021
Study Design
- Enrollment
- 91 participants (actual)
- Allocation
- NA
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Dose EscalationPF-06753512
Primary Outcome Measure
Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs) [ Time Frame: Baseline up to 6 months after End of Treatment (EOT; 52 months in maximum) ]
Locations (19)
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By research site
Banner-University Medical Center Tucson· Tucson, AZThe University of Arizona Cancer Center-North Campus· Tucson, AZSmilow Cancer Hospital at Yale-New Haven· New Haven, CTSmilow Cancer Hospital Phase 1 Unit· New Haven, CTNational Institutes of Health Clinical Center· Bethesda, MDGU Research Network· Omaha, NE
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