Skip to content

ZELBORAF Special Drug Use Surveillance (Malignant Melanoma)

ZELBORAF Special Drug Use Surveillance (Malignant Melanoma) - ZELBORAF Special Drug Use Surveillance (Malignant Melanoma)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000016583
Enrollment
500
Registered
2015-02-26
Start date
2015-02-26
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Malignant Melanoma

Interventions

None listed

Sponsors

Chugai Pharmaceutical Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients planning to use Zelboraf during the enrollment period

Exclusion criteria

Exclusion criteria: No criteria

Design outcomes

Primary

MeasureTime frame
Adverse reaction incidence

Secondary

MeasureTime frame
Effectiveness OS

Countries

Japan

Contacts

Public ContactShinichi Matsuda

Chugai Pharmaceutical Co. Ltd. Safety science Dept

matsudasni@chugai-pharm.co.jp03-3281-6611

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026