A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABSK-011 in Patients With Advanced Solid Tumor

Targeted Disease(s):
Lung Cancer

Purpose of Study:

The escalation part will evaluate the safety, tolerability, PK and recommended dose of expansion (RDE) of oral ABSK-011 in patients with advanced solid tumors. The expansion part of oral ABSK-011 at RDE will be followed for further evaluating safety and tolerability in patients with FGF19 overexpression advanced HCC. Preliminary antitumor activity will also be assessed.

Study Dates:
February 26, 2020 - December 31, 2027

Type of Study:
Pre-Market

Study Design:
Controlled Design

Study Location:
Nationwide

Sponsors:

Abbisko Therapeutics Co., Ltd.

Contact:

Please contact the site directly. All recruiting sites are listed on clinicaltrials.gov.

ClinicalTrails.gov Identifier:
NCT04906434

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