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AQUA07 in Patients With ALK-Positive Non-Small Cell Lung Cancer
Sponsor: Chugai Pharmaceutical
Summary
This is a first-in-human, Phase I, open-label, multicenter, multinational study, designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and anti-tumor activity of AQUA07 when administered as single agent and in combination with lorlatinib in patients with ALK positive non-small cell lung cancer.
Official title: A Phase I, Open-Label, Multicenter, Dose Escalation and Cohort Expansion Study of AQUA07 Monotherapy and Combination Therapy in Patients With Anaplastic Lymphoma Kinase-Positive Non-Small Cell Lung Cancer
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
102
Start Date
2026-07-24
Completion Date
2030-08-31
Last Updated
2026-08-19
Healthy Volunteers
No
Conditions
Interventions
AQUA07
AQUA07 administrated orally
Lorlatinib
Lorlatinib administerd orally
Locations (5)
Aichi Cancer Center Hospital
Nagoya, Aichi-ken, Japan
Kindai University Hospital
Sakai, Osaka, Japan
Shizuoka Cancer Center
Nagaizumi-cho, Shizuoka, Japan
National Cancer Center Hospital
Chuo-ku, Tokyo, Japan
The Cancer Institute Hospital of JFCR (Japanese Foundation for Cancer Research)
Koto-Ku, Tokyo, Japan