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ALECENSA Drug Use Surveillance

ALECENSA Drug Use Surveillance - ALECENSA Drug Use Surveillance

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000061763
Enrollment
100
Registered
2026-06-02
Start date
2026-06-01
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

To confirm the following under actual conditions of use of Alectinib Hydrochloride Capsules (hereinafter, this drug) in ALK fusion gene-positive patients with advanced or recurrent solid tumors Non-small cell lung cancer (NSCLC) and inflammatory myofifibroblastic tumors (IMT): Safety in children (under 16 years old) NSCLC and Non-IMT Solid Carcinomas: Efficacy and Safety

Interventions

None listed

Sponsors

Chugai Pharmaceutical Co. Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Non-small cell lung cancer (NSCLC) and inflammatory myofifibroblastic tumors (IMT): Safety in children (under 16 years old) NSCLC and Non-IMT Solid Carcinomas: Efficacy and Safety

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Efficacy: Response rate based on the attending physician's assessment Safety: Incidence rate of adverse events (by MedDRA PT, by severity, by grade)

Countries

Japan

Contacts

Public ContactAyako Murayama

Chugai Pharmaceutical Co. Ltd Safety Science 2 Department

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

Outcome results

None listed

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