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NCT06091124RECRUITINGanonymous

A Prospective, Single-arm, Exploratory Study on the Efficacy and Safety of Neoadjuvant Adebrelimab Plus Etoposide and Cisplatin in Patients With Neuroendocrine Bladder Carcinoma

Sponsor

Source record

RenJi Hospital

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

PD-1 receptor inhibition via adebrelimab, combined with cytotoxic agents etoposide and cisplatin.

Indication / condition

AI-normalized

Neuroendocrine Carcinoma of the Bladder

Intervention

Source record

Adebrelimab, Etoposide, Cisplatin, Radical Cystectomy

Source & freshness

Source record

NCT ID

NCT06091124

Original source

ClinicalTrials.gov

Source last updated

Dec 08, 2025

Ingested at

Jun 17, 2026

Internal sync

Jun 17, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT06091124

Title

A Prospective, Single-arm, Exploratory Study on the Efficacy and Safety of Neoadjuvant Adebrelimab Plus Etoposide and Cisplatin in Patients With Neuroendocrine Bladder Carcinoma

Sponsor

RenJi Hospital

Status

RECRUITING

Phase

Phase 2

Condition raw

Neuroendocrine Carcinoma of the Bladder, Bladder Cancer

Condition normalized

Neuroendocrine Carcinoma of the Bladder, Bladder Cancer

Modality raw

small molecule

Modality normalized

small molecule

Target raw

PD-1 receptor inhibition via adebrelimab, combined with cytotoxic agents etoposide and cisplatin.

Target normalized

PD-1 receptor inhibition via adebrelimab, combined with cytotoxic agents etoposide and cisplatin.

Interventions

Adebrelimab, Etoposide, Cisplatin, Radical Cystectomy

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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