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NCT07517653

Neoadjuvant SHR-1701 Plus Famitinib With Response-guided Adjuvant Therapy in Resectable Mucosal Melanoma

Not yet recruiting Phase 2 Last updated 8 April 2026
What this trial tests

Phase 2 trial testing SHR-1701 in Melanoma in 70 participants. Not yet recruiting.

Timeline
1 April 2026
Primary endpoint
30 November 2028
30 December 2028

Quick facts

Lead sponsorShanghai Zhongshan Hospital
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment70
Start date1 April 2026
Primary completion30 November 2028
Estimated completion30 December 2028

Drugs / interventions tested

Conditions studied

Sponsor

Shanghai Zhongshan Hospital

Who can join

Adults 18 to 75, any sex, with Melanoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to investigate the efficacy and safety of SHR-1701 in combination with famitinib in the perioperative treatment of mucosal melanoma

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of SHR-1701

Trials testing the same drug.

Other recruiting trials for Melanoma

Currently open trials in the same condition.

Other Shanghai Zhongshan Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07517653.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing