Clinical trial
Efficacy and Safety of Iparomlimab and Tuvonralimab Injection(Anti-PD-1/CTLA-4 Bispecific Antibody) Combined With Recombinant Human GM-CSF Oncolytic HSV-2 (OH2) Injection (Vero Cells) for Perioperative Treatment of Stage III Resectable Acral Melanoma: A Prospective, Randomized, Controlled, Multicenter Clinical Study
NCT07854522 is registered in ClinicalTrials.gov with Peking University Cancer Hospital & Institute as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Efficacy and Safety of Iparomlimab and Tuvonralimab Injection(Anti-PD-1/CTLA-4 Bispecific Antibody) Combined With Recombinant Human GM-CSF Oncolytic HSV-2 (OH2) Injection (Vero Cells) for Perioperative Treatment of Stage III Resectable Acral Melanoma: A Prospective, Randomized, Controlled, Multicenter Clinical Study
- Lead sponsor
- Peking University Cancer Hospital & Institute
- Phase
- Phase 4
- Overall status
- Not yet recruiting
- Start date
- October 31, 2026
- Completion date
- June 30, 2030
- Enrollment
- 76 (estimated)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
acral melanoma, melanoma