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Prospective study of safety and efficacy of tislelizumab in adjuvant therapy for urothelial carcinoma

Prospective study of safety and efficacy of tislelizumab in adjuvant therapy for urothelial carcinoma

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068589
Enrollment
Unknown
Registered
2023-02-24
Start date
2023-02-20
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urothelial carcinoma

Interventions

Test group:Terarelizumab

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with urothelial carcinoma ( including bladder cancer, ureteral cancer and renal pelvic cancer ) ; patients without distant metastasis within 3 months after radical resection ; preoperative neoadjuvant patients were ypT2-4a or ypN +. Preoperative non-neoadjuvant : pT3-T4a or pTX N +

Exclusion criteria

Exclusion criteria: suffering from severe bleeding tendency or blood coagulation disease; patients with severe heart, brain, lung, liver, kidney and other visceral diseases or nervous system lesions; the researchers believe that other reasons are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
1 year disease-free recurrence rate;

Secondary

MeasureTime frame
1-year completion rate of immunotherapy;incidence of adverse reactions;no disease recurrence rate in patients with bladder cancer and upper urothelial carcinoma for 1 year;

Countries

China

Contacts

Public ContactZhang Yaqun

NO.1 DaHua Road, Dong Dan, Beijing

zhangyaqun@yeah.net13671330920

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026