πŸ›οΈ Verified NIH Record β€’ Updated 2023-04-05

DPX-Survivac and Pembrolizumab With and Without Intermittent Low-Dose Cyclophosphamide, in Subjects With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (NCT04920617)

A Phase 2b, Open-label, Multicenter, Randomized Parallel-Group, Two-Stage, Study of an Immunotherapeutic Treatment DPX-Survivac and Pembrolizumab, With and Without Intermittent Low-Dose Cyclophosphamide, in Subjects With Relapsed/Refractory Diffuse Large B-Cell Lymphoma (VITALIZE)

🟒 Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: ImmunoVaccine Technologies, Inc. (IMV Inc.)

🩺 Plain-English Summary (8th-Grade Level)

This 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.

Who can join: Review the eligibility criteria below.

Location: Compassionate Cancer Care Medical Group β€” Fountain Valley, California

Age range: 18 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (50 Sites)

Showing the first 25 of 50 sites.

  • Compassionate Cancer Care Medical Group β€” Fountain Valley, California
  • Boca Raton Regional Hospital β€” Boca Raton, Florida
  • BRCR Medical Center Inc. β€” Hollywood, Florida
  • BRCR Medical Center Inc. β€” Plantation, Florida
  • Comprehensive Hematology and Oncology β€” St. Petersburg, Florida
  • Blood and Marrow Transplant Group of Georgia β€” Atlanta, Georgia
  • Indiana University Health Melvin and Bren Simon Cancer Center β€” Indianapolis, Indiana
  • Tulane Cancer Center Office of Clinical Research β€” New Orleans, Louisiana
  • Oncology Hematology West, PC dba Nebraska Cancer Specialists β€” Omaha, Nebraska
  • Christus St. Vincent Regional Cancer Center β€” Santa Fe, New Mexico
  • Brody School of Medicine at East Carolina University β€” Greenville, North Carolina
  • Gabrail Cancer Center Research β€” Canton, Ohio
  • University of Toledo Medical Center β€” Toledo, Ohio
  • Toledo Clinic Cancer Center β€” Toledo, Ohio
  • Allegheny Health Network (AHN) West Penn Hospital β€” Pittsburgh, Pennsylvania
  • Reading Hospital - McGlinn Cancer Institute β€” West Reading, Pennsylvania
  • Prairie Lakes Health Care System β€” Watertown, South Dakota
  • Royal Adelaide Hospital β€” Adelaide, South Australia
  • Epworth Freemasons Hospital β€” Melbourne, Victoria
  • Box Hill Hospital β€” Melbourne, Victoria
  • Westmead Hospital β€” Westmead,
  • Saskatoon Cancer Center β€” Saskatoon, Saskatchewan
  • HΓ΄pital Avicenne β€” Bobigny,
  • Centre d'Oncologie de Gentilly β€” Nancy,
  • HΓ΄pital PrivΓ© du Confluent β€” Nantes,

πŸ“ž Contact the Study Coordinator

Phone: (714) 698-0300

Email: ericlee@compcancercare.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—