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NCT07207824: HERO

DV+BCG in HER2-Expressing, BCG-Naïve High-Risk NMIBC

Not yet recruiting Phase 3 Last updated 6 October 2025
What this trial tests

Phase 3 trial testing Active Comparator: BCG induction and maintenance in Bladder (Urothelial, Transitional Cell) Cancer in 182 participants. Not yet recruiting.

Timeline
1 December 2025
Primary endpoint
1 June 2030
1 December 2030

Quick facts

Lead sponsorFudan University
PhasePhase 3
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment182
Start date1 December 2025
Primary completion1 June 2030
Estimated completion1 December 2030
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fudan University

Who can join

18 and older, any sex, with Bladder (Urothelial, Transitional Cell) Cancer or NMIBC. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to learn about the safety and effects of the study medicine (Disitamab Vedotin) in people with non-muscle invasive bladder cancer. This study is seeking participants whose bladder cancer is still in early stages, has not spread outside of the bladder, has been removed with surgery, and is high risk. Each participant was assigned to one of two study treatment groups: One group is given Disitamab Vedotin and BCG.The second group is given BCG only and will not receive Disitamab Vedotin.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Bladder (Urothelial, Transitional Cell) Cancer

Currently open trials in the same condition.

Other Fudan University 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/NCT07207824.

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