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TECENTRIQ Drug Use Surveillance(advanced or recurrent non-small cell lung cancer)

TECENTRIQ Drug Use Surveillance(advanced or recurrent non-small cell lung cancer) - TECENTRIQ Drug Use Surveillance(NSCLC)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000031978
Enrollment
1000
Registered
2018-04-17
Start date
2018-04-18
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

non-small cell lung cancer

Interventions

None listed

Sponsors

Chugai Pharmaceutical Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients who are scheduled to receive TECENTRIQ at contracted institutions during this surveillance's enrollment period.

Exclusion criteria

Exclusion criteria: No criteria

Design outcomes

Primary

MeasureTime frame
The incidence of ADRs.

Secondary

MeasureTime frame
- The time of onset of ADRs. - The treatment status and outcome of ADRs. - The incidence of ADRs for each patient baseline characteristic.

Countries

Japan

Contacts

Public ContactAyaka Shimizu

Chugai Pharmaceutical Co. Ltd. Real world data science Dept.

shimizuayk@chugai-pharm.co.jp03-3273-0905

Outcome results

None listed

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