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Study of NXP900 With Lorlatinib in ALK+ Lung Cancer

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NCT07784959 · readout ≤ 370 d

Sponsored by Nuvectis Pharma, Inc. (industry) · NVCT — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
54estimated
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 2026-08-25

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-08-17actualWhen the study began enrolling
Primary completionAug 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionFeb 2028estimatedThe whole study's end, after follow-up
First posted2026-08-25actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • ALK Positive
  • ALK Positive Non-small Cell Lung Cancer
  • NSCLC
  • ALK+ Non-Small-Cell Lung Carcinoma

Interventions

  • Drug: NXP900
  • Drug: Lorlatinib

Primary outcomes

what the primary-completion date above is the date OF
Number of patients with treatment related adverse events and/or clinical laboratory abnormalities
measured Up to 30 days post treatment
Objective response rate (ORR)
measured Up to approximately 12 months
Duration of Response (DoR)
measured Up to approximately 12 months
Disease Control Rate (DCR)
measured Up to approximately 12 months

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