RecruitingPHASE1, PHASE2NCT06940739
A Study to Investigate the Safety and Efficacy of IOV-3001 in Adults With Advanced Melanoma Who Will Receive Lifileucel
Studying Uveal melanoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Iovance Biotherapeutics, Inc.
- Principal Investigator
- Iovance Biotherapeutics Study TeamIovance Biotherapeutics
- Intervention
- IOV-3001(biological)
- Enrollment
- 42 target
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2025 – 2032
Study locations (4)
- SCRI Oncology Partners- Denver, Denver, Colorado, United States
- UNC Hospitals, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States
- Sarah Cannon Research Institute, Nashville, Tennessee, United States
- Greenslopes Private Hospital, Greenslopes, Queensland, Australia
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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