drugset / Trial / NCT02616185

A Phase 1 Study To Evaluate Escalating Doses Of A Vaccine-Based Immunotherapy Regimen For Prostate Cancer (PrCa VBIR)

NCT02616185 ↗

Phase 1 Terminated 91 enrolled Pfizer
NaSequentialOpen-labelTreatment

Summary

The study will evaluate the safety, pharmacokinetics and pharmacodynamics of increasing doses of a vaccine-based immunotherapy regimen for patients with prostate cancer.

Timeline

Start
2015-12-30
Primary completion
2021-02-23
Completion
2021-02-23

Outcome

Outcome not reported

Stopped (Business): “Due to strategic evaluation of PF-06753512 (VBIR-1) within context of Pfizer's oncology portfolio, decision not based on any safety or regulatory concerns.”

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-06755990 Vaccine — Intramuscular
Subject PF-06755992 Unknown — Intramuscular
Subject PF-06801591 Monoclonal antibody 130 mg Subcutaneous
Subject PF-06801591 Monoclonal antibody 300 mg Subcutaneous
Subject Tremelimumab Monoclonal antibody 40 mg Subcutaneous
Subject Tremelimumab Monoclonal antibody 80 mg Subcutaneous

Indications