drugset / Trial / NCT02616185
A Phase 1 Study To Evaluate Escalating Doses Of A Vaccine-Based Immunotherapy Regimen For Prostate Cancer (PrCa VBIR)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |