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Clinical Trials in China / NCT06696742
Recruiting Phase 2

PD1 Inhibitors Combined With Clostridium Butyricum for Urothelial Carcinoma

NCT06696742 · tracked via the Priya Life Science China tracker
Sponsor
The First Affiliated Hospital with Nanjing Medical University
Phase
Phase 2
Started
2024-02-01
Last updated
2024-11-20

Condition(s) studied

Bladder (Urothelial, Transitional Cell) Cancer

Investigational drug(s) / intervention(s)

Clostridium Butyricum Tablets →Cisplatin →

Clostridium Butyricum Tablets: Gemcitabine and Cisplatin combined with Clostridium Butyricum Tablets

Cisplatin: Gemcitabine and Cisplatin

Study summary

This study intends to explore whether the combination of Clostridium butyricum can improve the current situation of poor anti-PD1 treatment effect in patients with bladder cancer.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: For Neoadjuvant therapy: * T2-T4aN0M0 bladder patients For Adjuvant therapy: * Postoperative pathological stage T3-T4 and/or lymph node metastasis were positive. Exclusion Criteria: * The researchers evaluated the patients who could not tolerate radical surgery; * Previously received systemic chemotherapy or immunotherapy; * There are active autoimmune diseases requiring systemic treatment or other diseases requiring long-term use of a large number of hormones and other immunosuppressants; * Have had major surgery or major trauma within 28 days before joining the group; * Vaccinated with live vaccine within 28 days before joining the group.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Nanjing Medical University Nanjing Jiangsu Recruiting

More The First Affiliated Hospital with Nanjing Medical University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06696742 on ClinicalTrials.gov ↗ ← All trials in China