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Study details
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DPX-Survivac and Pembrolizumab Trial

ImmunoVaccine Technologies, Inc. (IMV Inc.)
NCT IDNCT04920617ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

102

Study length

about 3.9 years

Ages

18+

Locations

17 sites in CA, FL, GA +8

What this study is about

Researchers are testing DPX-Survivac, pembrolizumab, with or without low-dose cyclophosphamide (CPA), in people with relapsed or refractory diffuse large B-cell lymphoma. The trial will last for about 1412 days.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take CPA
  • 2.Take DPX-Survivac
  • 3.Take Pembrolizumab

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

pembrolizumab (Immune checkpoint inhibitor; blocks PD-1 to boost T-cell attack on cancer)

Drug routes

infusion

Endpoints

Primary: Objective response rate (ORR) in each of the study arms

Secondary: Changes in Patient Reported Outcomes using the EQ-5D-5L Assessment, Changes in Patient Reported Outcomes using the FACT-Lym Assessment, Complete response (CR) rate in each of the study arms, Disease control rate (DCR) in each of the study arms, Duration of response (DOR) in each of the study arms, Progression-Free Survival in each of the study arms, Rate of Adverse Events using the Common Terminology Criteria for Adverse Events (CTCAE) v5.0 in each of the study arms

Body systems

Oncology