An Relative Bioavailability Study of BH006 for Injection in Healthy Subjects

EARLY_PHASE1Not yet recruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

May 31, 2024

Primary Completion Date

September 30, 2024

Study Completion Date

December 31, 2024

Conditions
Bioavailability
Interventions
DRUG

BH006 for injection

According to the random administration plan, the test product BH006 \[(fosaprepitant and palonosetron) for injection\] 150mg/0.25mg or the reference product \[EMEND® (fosaprepitant) for injection 150 mg + Palonosetron hydrochloride injection 0.25 mg) were injected, and crossovered after a sufficient washing period (14 days), dosing is carried out for the second cycle study.

DRUG

Fosaprepitant for injection+Palonosetron hydrochloride injection

According to the random administration plan, the test product BH006 \[(fosaprepitant and palonosetron) for injection\] 150mg/0.25mg or the reference product \[EMEND® (fosaprepitant) for injection 150 mg + Palonosetron hydrochloride injection 0.25 mg) were injected, and crossovered after a sufficient washing period (14 days), dosing is carried out for the second cycle study.

All Listed Sponsors
lead

Zhuhai Beihai Biotech Co., Ltd

INDUSTRY

NCT06427681 - An Relative Bioavailability Study of BH006 for Injection in Healthy Subjects | Biotech Hunter | Biotech Hunter