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A Study to Evaluate the Pharmacokinetics, Efficacy, Safety and Immunogenicity of Xdivane versus Opdivo® in Patients with Resected Melanoma

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-522307-14-00
Acronym
0439-24
Enrollment
34
Registered
2025-12-08
Start date
2026-01-19
Completion date
Unknown
Last updated
2025-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma

Interventions

None listed

Sponsors

Intas Pharmaceuticals Limited
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Romania, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026