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AQUA07 in Patients With ALK-Positive Non-Small Cell Lung Cancer

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NCT07617337 · readout in 1,473 d

Sponsored by Chugai Pharmaceutical (industry) · 4519.T — their whole pipeline →.

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
102estimated
Sites
5
Country
Japan

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
Start2026-07-24actualWhen the study began enrolling
Primary completion2030-08-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-08-31estimatedThe whole study's end, after follow-up
First posted2026-06-01actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • ALK Positive Non-small Cell Lung Cancer

Interventions

  • Drug: AQUA07
  • Drug: Lorlatinib

Primary outcomes

what the primary-completion date above is the date OF
Adverse events [PartA,B]
measured From screening until study completion, treatment discontinuation or post-treatment follow up (up to approximately 48 months)
Dose-Limiting Toxicities (DLTs) [PartA,B]
measured From cycle 0 day1 (if applicable) or cycle 1 day 1 to cycle 1 day 21 (each cycle is 21 days)
Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD) and Recommendation Dose (RD) Determination [PartA,B]
measured From cycle 0 day1 (if applicable) or cycle 1 day 1 to cycle 1 day 21 (each cycle is 21 days)

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