RecruitingPhase 2NCT06210490

A Clinical Study of the Efficacy and Safety of Disitamab Vedotin in Combination With Radiotherapy for the Adjuvant Treatment of HER2 Overexpressing UTUC Patients With High Risk Factors for Recurrence After Radical Surgery

Studying Upper tract urothelial carcinoma

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Key facts

Sponsor
Peking University First Hospital
Intervention
Disitamab Vedotin(drug)
Enrollment
60 target
Eligibility
18 years · All sexes
Timeline
20242028

Study locations (1)

Collaborators

Peking University First Hospital Miyun Hospital

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.

Open NCT06210490 on ClinicalTrials.gov

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