A Phase 1, Randomized, Crossover Study to Evaluate the Relative Bioavailability and Food Effect of HRS-8080 in Healthy Subjects

PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

October 10, 2024

Primary Completion Date

October 30, 2024

Study Completion Date

November 15, 2024

Conditions
Breast Cancer
Interventions
DRUG

HRS-8080

"Medication regimen A~Drug:~600mg, Old process tablets,NPO~Medication regimen B~Drug:~600mg, New process tablets,NPO~Medication regimen C~Drug:~600mg, New process tablets,PC.,low-fat diet~Medication regimen D~Drug:~600mg, New process tablets,PC.,high-fat diet"

Trial Locations (1)

230001

The Frist Affiliated Hospital of USTC (Anhui Provincial Hospital), Hefei

All Listed Sponsors
lead

Shandong Suncadia Medicine Co., Ltd.

INDUSTRY

NCT06619873 - A Phase 1, Randomized, Crossover Study to Evaluate the Relative Bioavailability and Food Effect of HRS-8080 in Healthy Subjects | Biotech Hunter | Biotech Hunter