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Bavencio Intravenous200 mg Special Drug Use - results Survey (Curatively unresectable or metastatic renal cell carcinoma)

Bavencio Intravenous200 mg Special Drug Use - results Survey (Curatively unresectable or metastatic renal cell carcinoma) - Bavencio Special Drug Use-results Survey (Renal cell carcinoma)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000039476
Enrollment
250
Registered
2020-02-13
Start date
2019-12-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Curatively unresectable or metastatic renal cell carcinoma

Interventions

None listed

Sponsors

Merck Biopharma Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients who received at least one dose of Bavencio for Curatively unresectable or metastatic renal cell carcinoma during the enrollment period.

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Incidence of all Adverse drug reactions / all Adverse Events related to the Safety Specification

Secondary

MeasureTime frame
Effectiveness in terms of Best Overall Response and Overall Survival

Countries

Japan

Contacts

Public ContactTaito Ito

Merck Biopharma Co., Ltd. PMS Planning & Strategy, Medical Department

taito.ito@merckgroup.com03-6756-0805

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026