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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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take CPA
  • 2.Take DPX-Survivac
  • 3.Take Pembrolizumab
PhasePhase 2
DrugPembrolizumab
Routeinfusion
Primary goalObjective response rate (ORR) in each of the study arms

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low10%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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