Efficacy of Daromun Neoadjuvant Intratumoral Treatment in Clinical Stage IIIB/C/D Melanoma Patients (NCT03567889)
An Open-Label, Randomized, Controlled Multi-Center Study of The Efficacy of Daromun (L19IL2 + L19TNF) Neoadjuvant Intratumoral Treatment Followed by Surgery and Adjuvant Therapy Versus Surgery and Adjuvant Therapy in Clinical Stage IIIB/C/D Melanoma Patients
๐ฉบ Plain-English Summary (8th-Grade Level)
The trial aims to evaluate the efficacy of Daromun neoadjuvant treatment followed by surgery and adjuvant therapy to improve in a statistically significant manner the recurrence-free survival (RFS) of Stage IIIB/C/D melanoma patients with respect to the standard of care (surgery and adjuvant therapy).
Who can join: Review the eligibility criteria below.
Location: Mayo Clinic Hospital โ Phoenix, Arizona
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (37 Sites)
Showing the first 25 of 37 sites.
- Mayo Clinic Hospital โ Phoenix, Arizona
- UC San Diego Moores Cancer Center โ La Jolla, California
- UC Irvine Health-Chao Family Comprehensive Cancer Center โ Orange, California
- Moffitt Cancer Center โ Tampa, Florida
- Winship Cancer Institute, Emory university โ Atlanta, Georgia
- Rush University Medical Center โ Chicago, Illinois
- University of Iowa Hospitals and Clinics โ Iowa City, Iowa
- Mayo Clinic โ Rochester, Minnesota
- Rutgers Cancer Institute, 195 Little Albany Street โ New Brunswick, New Jersey
- Ambulatory Care Center at NYC Langarone Health โ New York, New York
- Memorial Sloan Kettering Cancer Center - Main Campus โ Ney York, New York
- Duke University Medical Center - Duke Cancer Center โ Durham, North Carolina
- Ohio State University Wexner Medical Center โ Columbus, Ohio
- St. Luke's Cancer Center, Clinical Trial, 3rd floor, 1600 St. Luke's Blvd. โ Easton, Pennsylvania
- Penn State Cancer Institute โ Hershey, Pennsylvania
- Fox Chase Cancer Center 333 Cottman Avenue โ Philadelphia, Pennsylvania
- The University of Texas M.D. Anderson Cancer Center โ Houston, Texas
- Huntsman Cancer Institute, University of Utah 2000 Circle of Hope โ Salt Lake City, UT, Utah
- VCU - McGlothlin Medical Education Center โ Richmond, Virginia
- Hospital Universitari Germans Trias i Pujol โ Badalona, Barcelona
- Hospital de la Santa Creu i Sant Pau โ Barcelona, Barcelona
- Fir Huvh Fundacio Institut De Recerca Hospital Universitari Vall De Hebron โ Barcelona, Barcelona
- Hospital Clinic Barcelona โ Barcelona, Barcelona
- El Hospital Universitario De Gran Canaria Dr. Negrin โ Las Palmas de Gran Canaria, Canarie
- Fundacion Onkologikoa Fundazioa โ Donostia / San Sebastian, Gipuzkoa
๐ Contact the Study Coordinator
Phone: +41 (0) 43 544 88 02
Email: sheila.dakhel@philogen.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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 ยง 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.
Explore by condition: All Melanoma Stage IIIB clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.