Real World Evaluation of Sotorasib Among Chinese Non-Small Cell Lung Cancer Patients

NCT07143513 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 102

Last updated 2026-04-07

No results posted yet for this study

Summary

The primary objective of this study is to characterize the safety profile of sotorasib.

Conditions

Interventions

DRUG

Sotorasib

Participants will have received sotorasib orally daily until disease progression or unacceptable toxicity.

Sponsors & Collaborators

Principal Investigators

  • MD · Amgen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-11
Primary Completion
2025-12-07
Completion
2025-12-07
FDA Drug
Yes

Countries

  • China

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07143513 on ClinicalTrials.gov