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Active, not recruiting Phase 2 Interventional

Study of an Immunotherapeutic, DPX-Survivac, in Combination With Low Dose Cyclophosphamide & Pembrolizumab, in Subjects With Selected Advanced & Recurrent Solid Tumors

ClinicalTrials.gov ID: NCT03836352

Public ClinicalTrials.gov record NCT03836352. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 1:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Open-label, Multicenter, Study of an Immunotherapeutic Treatment, DPX-Survivac in Combination With Low Dose Cyclophosphamide and Pembrolizumab, in Subjects With Selected Advanced and Recurrent Solid Tumours.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will assess the safety and efficacy of DPX-Survivac and low dose cyclophosphamide with pembrolizumab in subjects with selected advanced and recurrent solid tumours.

Study identification

NCT ID
NCT03836352
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
184 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 20, 2018
Primary completion
Dec 30, 2023
Completion
Dec 30, 2023
Last update posted
Mar 30, 2022

2018 – 2023

United States locations

U.S. sites
15
U.S. states
11
U.S. cities
15
Facility City State ZIP Site status
The University of Arizona Cancer Center Tucson Arizona 58724
Cedars Sinai Medical Center: Samuel Oschin Comprehensive Cancer Center Los Angeles California 90048
Boca Raton Regional Hospital, Lynn Cancer Institute Boca Raton Florida 33486
Hematology Oncology Associates of the Treasure Coast Port Saint Lucie Florida 34952
Comprehensive Hematology and Oncology St. Petersburg Florida 33709
Winship Cancer Institute: The Emory Clinic Atlanta Georgia 30322
James Brown Graham Cancer Center:University of Louisville Hospital Louisville Kentucky 40202
Ochsner Cancer Institute New Orleans Louisiana 70121
Allina Health, Virginia Piper Cancer Institute Minneapolis Minnesota 55407
Christus St. Vincent Regional Cancer Center Santa Fe New Mexico 87505
NYU Winthrop Hospital Mineola New York 11501
Montefiore Medical Center The Bronx New York 10461
University of Toledo Toledo Ohio 43614
Mary Crowley Cancer Research Center Dallas Texas 75230
MD Anderson Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03836352, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 30, 2022 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03836352 live on ClinicalTrials.gov.

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