πŸ›οΈ Verified NIH Record β€’ Updated 2022-03-28

Study of an Immunotherapeutic, DPX-Survivac, in Combination With Low Dose Cyclophosphamide & Pembrolizumab, in Subjects With Selected Advanced & Recurrent Solid Tumors (NCT03836352)

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.

πŸ”΅ Active, Not Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: ImmunoVaccine Technologies, Inc. (IMV Inc.)

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

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.

Who can join: Review the eligibility criteria below.

Location: The University of Arizona Cancer Center β€” Tucson, Arizona

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 (23 Sites)

  • The University of Arizona Cancer Center β€” Tucson, Arizona
  • Cedars Sinai Medical Center: Samuel Oschin Comprehensive Cancer Center β€” Los Angeles, California
  • Boca Raton Regional Hospital, Lynn Cancer Institute β€” Boca Raton, Florida
  • Hematology Oncology Associates of the Treasure Coast β€” Port Saint Lucie, Florida
  • Comprehensive Hematology and Oncology β€” St. Petersburg, Florida
  • Winship Cancer Institute: The Emory Clinic β€” Atlanta, Georgia
  • James Brown Graham Cancer Center:University of Louisville Hospital β€” Louisville, Kentucky
  • Ochsner Cancer Institute β€” New Orleans, Louisiana
  • Allina Health, Virginia Piper Cancer Institute β€” Minneapolis, Minnesota
  • Christus St. Vincent Regional Cancer Center β€” Santa Fe, New Mexico
  • NYU Winthrop Hospital β€” Mineola, New York
  • Montefiore Medical Center β€” The Bronx, New York
  • University of Toledo β€” Toledo, Ohio
  • Mary Crowley Cancer Research Center β€” Dallas, Texas
  • MD Anderson β€” Houston, Texas
  • William Osler Health System β€” Brampton, Ontario
  • Juravinski Cancer Center β€” Hamilton, Ontario
  • Southlake Regional Health Center β€” Newmarket, Ontario
  • The Ottawa Hospital β€” Ottawa, Ontario
  • Sunnybrook Research Institute β€” Toronto, Ontario
  • Centre hospitalier de l'UniversitΓ© de MontrΓ©al (CHUM) β€” Montreal, Quebec
  • McGill University Health Center β€” Montreal, Quebec
  • CHU de QuΓ©bec-UniversitΓ© Laval β€” QuΓ©bec, Quebec

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.

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πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  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†—