CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 47 enrolled
Drug / intervention
Pembrolizumab +2 moredrug
Likely dose
Pembrolizumab 200 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03029403
NCT03029403Phase 2Active

A Phase 2 Study of Pembrolizumab (MK-3475), DPX-Survivac Vaccine and Low Dose of Cyclophosphamide Combination in Patients With Advanced Ovarian, Primary Peritoneal or Fallopian Tube Cancer

University Health Network, Toronto·interventional·Posted Jan 24, 2017·Updated Sep 19, 2025

In Brief

A Phase 2 clinical trial evaluating Pembrolizumab, DPX-Survivac, and 1 other intervention for Advanced Cancer and 3 related conditions. Active but no longer recruiting, targeting 47 participants across 1 site.

Detailed Summary

This is a phase 2 study whose purpose is to see whether the combination of of pembrolizumab, DPX-Survivac vaccine and low-dose cyclophosphamide has anti-tumor activity in patients with advanced epithelial ovarian, fallopian tube or primary peritoneal cancer. DPX-Survivac is an investigational vaccine. A vaccine is a substance that is often given to stimulate the body's immune system (the structure and processes in the body that protects against harmful substances) to help prevent against certain diseases. DPX-Survivac is a vaccine that may teach the immune system to recognize cancer cells and to kill them. Pembrolizumab is a drug that is approved for the treatment of a certain type of melanoma (a type of skin cancer) and non-small cell lung cancer. Pembrolizumab blocks the function of a protein called programmed cell death receptor-1 (PD-1). PD-1 works by keeping the immune system from destroying cancer cells. Stopping PD-1 from working may help the immune system to fight cancer cells. Cyclophosphamide is chemotherapy drug that is approved for the treatment of various cancers alone and in combination with other drugs.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

Phase 2ActiveOverdue
2017201820192020202120222023202420252026
First PostedJan 24, 2017
Enrollment StartFeb 12, 2018
Primary CompletionDec 12, 2025
Study CompletionApr 12, 2026
TodayJul 2, 2026
Enrollment to primary: 7.8 yearsPosted 9.4 years ago

Interventions

Pembrolizumabdrug

Given intravenously in clinic, at 200 mg, on Day 1 of every 21-day cycle.

DPX-Survivacbiological

Given by injection under the skin of the upper thigh in clinic. Participants will receive one priming dose of 0.25 mL of DPX-Survivac on Cycle 1 Day 1. After about 6 weeks, participants will receive an additional boosting dose of 0.25 or 0.5 mL DPX-Survivac.

Cyclophosphamidedrug

Given orally, at 50 mg, twice a day, starting about 7 days before Cycle 1 Day 1, then continue 7 days off, 7 days on.