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A Prospective, Single-arm, Exploratory Study on the Efficacy and Safety of Neoadjuvant Adebrelimab Plus Etoposide and Cisplatin in Patients With Neuroendocrine Bladder Carcinoma
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 17, 2026
NCT ID
NCT06091124
Status
RECRUITING
Phase
Phase 2
Sponsor
RenJi Hospital
Executive brief
Investment-Ready Snapshot
The clinical trial, sponsored by RenJi Hospital, is exploring the efficacy and safety of a novel neoadjuvant therapy combining adebrelimab, etoposide, and cisplatin for patients with neuroendocrine bladder carcinoma. Given the rarity of this cancer type and the limited treatment options currently available, successful outcomes could position this combination therapy as a significant advancement in the treatment landscape. The trial's focus on pathologic complete response rates and safety profiles will be critical in assessing its commercial viability. The market for bladder cancer therapies is competitive, with established players like Merck and Bristol-Myers Squibb, but the unique approach targeting neuroendocrine components may provide a niche opportunity. Diligence should consider the regulatory landscape and potential for expedited pathways given the unmet medical need.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06091124
Indication
Neuroendocrine Carcinoma of the Bladder
Modality
small molecule
Target
PD-1 receptor inhibition via adebrelimab, combined with cytotoxic agents etoposide and cisplatin.
Intervention
Adebrelimab, Etoposide, Cisplatin, Radical Cystectomy
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.