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

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NCT07143513

Sponsored by Amgen (industry) · AMGN — their whole pipeline →.

Phase
Status
Completed
Study type
Observational
Enrollment
102actual
Sites
3
Country
China

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-08-11actualWhen the study began enrolling
Primary completion2025-12-07actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-12-07actualThe whole study's end, after follow-up
First posted2025-08-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-04-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Non-Small Cell Lung Cancer

Intervention

  • Drug: Sotorasib — also filed as AMG 510

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants with Treatment-emergent Adverse Events (TEAEs)
measured Up to approximately 4 years
Number of Participants with Adverse Events of Interest, Inclusive of Hepatotoxicity, Interstitial Lung Disease/Pneumonitis, and Renal Toxicity
measured Up to approximately 4 years
Number of Participants with Treatment-related Adverse Events (AEs)
measured Up to approximately 4 years
Number of Participants with Treatment-related AEs of Grade 3 or Worse
measured Up to approximately 4 years
Number of Participants with Serious Treatment-related AEs
measured Up to approximately 4 years
Number of Participants with Treatment-related AEs Leading to Treatment Discontinuation
measured Up to approximately 4 years
Number of Participants with Treatment-related AEs Leading to Dose Reduction
measured Up to approximately 4 years
Number of Participants with Treatment-related AEs Leading to Death
measured Up to approximately 4 years

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