ClinicalTrials.Veeva

Menu

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

Amgen logo

Amgen

Status

Enrolling

Conditions

Non-Small Cell Lung Cancer

Treatments

Drug: Sotorasib

Study type

Observational

Funder types

Industry

Identifiers

NCT07143513
20240175

Details and patient eligibility

About

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

Enrollment

115 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult (≥ 18 years) as of the index date.
  • KRAS p.G12C-mutated locally advanced or metastatic NSCLC.
  • Received at least 1 dose of sotorasib.
  • Receipt of at least 1 prior systemic therapy before use of sotorasib.
  • Obtained ICF, if required.

Exclusion criteria

  • Documentation of being a non-Chinese ethnicity.

Trial design

115 participants in 1 patient group

Chinese Participants Treated with Sotorasib
Description:
Adult participants with Kirsten rat sarcoma viral oncogene homolog (KRAS) p.G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC) and previously treated with at least 1 prior systemic therapy that have received sotorasib treatment in either location of BOAO Pilot Zone and Hong Kong SAR will be included in this cohort. The duration of evidence collection is from initiation of sotorasib to the end of study period, up to approximately 4 years from the date of the first available sotorasib use in BOAO Pilot Zone of around August 2021.
Treatment:
Drug: Sotorasib

Trial contacts and locations

3

Loading...

Central trial contact

Amgen Call Center

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems