SWE-NEO: Swedish NeoAdjuvant Trial Comparing Monotherapy to Combined Immunotherapy in Resectable Stage III Melanoma
- Sponsor
- Hildur Helgadottir
- Study ID
- NCT06794775
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- Malignant Melanoma Stage III
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab — DRUGAdjuvant monotherapy with Nivolumab
- Nivolumab + Ipilimumab — DRUGAdjuvant combination therapy with Nivolumab and Ipilimumab
Study Details
At present two studies (SWOG S1801 and NADINA) have demonstrated superiority when using neoadjuvant treatment compared to adjuvant treatment only, but no studies have compared PD-1 monotherapy (SWOG 1801 regimen) to the PD-1/CTLA-4 combination (NADINA regimen) therapy. The SWE-NEO study aims to compare these two regimens, where the PD-1/CTLA-4 combination is potentially more effective, but also associated with more side effects.
Key Dates
- Start date
- Jul 10, 2025
- Status verified
- Dec 2025
- Primary completion
- Apr 15, 2032
- Completion
- Apr 15, 2032
Study Design
- Enrollment
- 128 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: PD-1 inhibitor monotherapyMonotherapy with Nivolumab
- Experimental: PD-1/CTLA-4 inhibitor combination therapyCombination therapy with Nivolumab and Ipilimumab
Primary Outcome Measure
Event-free survival (EFS) [ Time Frame: From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months ]
Central Contacts
- Hildur Helgadottir, MD, PhD+46 8-123 734 15
- Roger Olofsson Bagge, Professor+46313421000