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OncoMatch/Clinical Trials/NCT04920617

DPX-Survivac and Pembrolizumab With and Without Intermittent Low-Dose Cyclophosphamide, in Subjects With Relapsed/Refractory Diffuse Large B-Cell Lymphoma

Is NCT04920617 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including DPX-Survivac and Pembrolizumab for relapsed diffuse large b-cell lymphoma.

Phase 2RecruitingImmunoVaccine Technologies, Inc. (IMV Inc.)NCT04920617Data as of May 2026

Treatment: DPX-Survivac · Pembrolizumab · CPAThis is a Phase 2b, randomized, open label study to assess the safety and efficacy of DPX-Survivac and pembrolizumab, with and without low-dose cyclophosphamide (CPA) in subjects with relapsed or refractory DLBCL.

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Extracted eligibility criteria

Cancer type

Diffuse Large B-Cell Lymphoma

Non-Hodgkin Lymphoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 2 prior lines

Must have received: anthracycline

prior treatment must have included an anthracycline

Must have received: CD20-targeted agent (rituximab)

prior treatment must have included ... rituximab (or another CD20-targeted agent)

Cannot have received: autologous stem cell transplant

Exception: allowed if >100 days prior to D0

Autologous stem cell transplant (ASCT) within <100 days prior to D0

Cannot have received: CAR-T cell therapy

Exception: allowed if >28 days prior to D0

Chimeric antigen receptor T cell (CAR-T) therapy within <28 days prior to D0

Cannot have received: chemotherapy

Exception: allowed if >28 days or >5 half-lives prior to D0

Chemotherapy ... within 28 days of D0 or 5 half-lives, whichever is shorter

Cannot have received: immunotherapy

Exception: allowed if >28 days or >5 half-lives prior to D0

Immunotherapy ... within 28 days of D0 or 5 half-lives, whichever is shorter

Cannot have received: radiotherapy

Exception: allowed if >14 days prior to D0

Radiotherapy within 14 days of day 0

Cannot have received: investigational agent

Exception: allowed if >28 days or >5 half-lives prior to D0

investigational agent treatment within 28 days of D0 or 5 half-lives, whichever is shorter

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Compassionate Cancer Care Medical Group · Fountain Valley, California
  • Boca Raton Regional Hospital · Boca Raton, Florida
  • BRCR Medical Center Inc. · Hollywood, Florida
  • BRCR Medical Center Inc. · Plantation, Florida
  • Comprehensive Hematology and Oncology · St. Petersburg, Florida

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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