Skip to content

Multi-institutional retrospective observational study of effectiveness and safety of treatment with Nivolmab for advanced or recurrent non-small cell lung cancer harboring EGFR mutation.

Multi-institutional retrospective observational study of effectiveness and safety of treatment with Nivolmab for advanced or recurrent non-small cell lung cancer harboring EGFR mutation. - Multi-institutional retrospective observational study of effectiveness and safety of treatment with Nivolmab for advanced or recurrent non-small cell lung cancer harboring EGFR mutation.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000025261
Enrollment
100
Registered
2016-12-31
Start date
2016-12-31
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

HANSHIN Oncology Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: NSCLC patients harboring EGFR gene mutation, who were treated with Nivolmab by the end of December 2016, are eligible for this study.

Exclusion criteria

Exclusion criteria: Nothing

Design outcomes

Primary

MeasureTime frame
effectiveness and safety

Secondary

MeasureTime frame
Response rate Progression free survival Overall survival Adverse events

Countries

Japan

Contacts

Public ContactYuki Akazawa

Toneyama National Hospital Department of Thoracic Oncology

akazaway@toneyama.go.jp06-6853-2001

Outcome results

None listed

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