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RECRUITING
NCT07617337
PHASE1

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

Sponsor: Chugai Pharmaceutical

View on ClinicalTrials.gov

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

Interventions

DRUG

AQUA07

AQUA07 administrated orally

DRUG

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