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A Study to Learn About Patients With Non-Small Cell Lung Cancer (NSCLC) Who Took Lorlatinib as Their First Treatment

← catalyst calendar

NCT07567352

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Status
Active, not recruiting
Study type
Observational
Enrollment
200actual
Sites
1
Country
United States

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
Start2026-05-01actualWhen the study began enrolling
Primary completion2026-07-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-07-31estimatedThe whole study's end, after follow-up
First posted2026-05-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Non-Small-Cell Lung
  • ALK-positive Advanced NSCLC
  • ALK-positive Non-small-cell Lung Cancer
  • ALK-positive NSCLC

Intervention

  • Drug: lorlatinib — also filed as Lorbrena

Primary outcomes

what the primary-completion date above is the date OF
Overall Treatment Duration of 1L Lorlatinib
measured From treatment initiation (on or after 3 March 2021) to end of follow-up (date of death or EHR activity end date) (data cutoff 31 March 2026)
Time to Discontinuation of 1L Lorlatinib
measured From treatment initiation (on or after 3 March 2021) to end of follow-up (date of death or EHR activity end date) (data cutoff 31 March 2026)
Number of Dose Changes of 1L Lorlatinib
measured From treatment initiation (on or after 3 March 2021) to end of follow-up (date of death or EHR activity end date) (data cutoff 31 March 2026)
Rate of Discontinuation of 1L Lorlatinib
measured From treatment initiation (on or after 3 March 2021) to end of follow-up (date of death or EHR activity end date) (data cutoff 31 March 2026)
Time to next treatment (TTNT)
measured From treatment initiation (on or after 3 March 2021) to end of follow-up (date of death or EHR activity end date) (data cutoff 31 March 2026)
Clinical Characteristic of Participants: Eastern Cooperative Oncology Group (ECOG) Performance Status
measured From treatment initiation (on or after 3 March 2021) to end of follow-up (date of death or EHR activity end date) (data cutoff 31 March 2026)

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