A Clinical Trial to Evaluate the Effect of Itraconazole and Rifampicin on ABSK021

PHASE1CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

April 11, 2023

Primary Completion Date

August 30, 2023

Study Completion Date

September 1, 2023

Conditions
Healthy Subjects
Interventions
DRUG

Part A ABSK201 and Itraconazole

Subjects will receive a single 10mg Oral administration of ABSK021 at C1D1, followed by a washout period of at least 14 days. The second cycle (C2): after the end of the first cycle, the subjects will receive 200 mg of C2D1-C2D24 Itraconazole oral liquid and a single 10 mg of ABSK021 Oral administration at C2D4.

DRUG

Part A ABSK201 and Rifampicin

Subjects will receive a single dose of 50 mg of ABSK021 Oral administration once at C1D1, followed by a washout period of at least 14 days. Subjects will receive 600 mg of Rifampicin capsules once a day at C2D1-C2D15 and a single dose of ABSK021 Oral administration at C2D7, with the dose of 50 mg.

Trial Locations (1)

201203

Huashan Hospital Fudan University, Shanghai

Sponsors
All Listed Sponsors
lead

Abbisko Therapeutics Co, Ltd

INDUSTRY

NCT06089733 - A Clinical Trial to Evaluate the Effect of Itraconazole and Rifampicin on ABSK021 | Biotech Hunter | Biotech Hunter