A Trial of CRB4101 in Healthy Subjects

PHASE1UnknownINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

November 16, 2022

Primary Completion Date

April 5, 2023

Study Completion Date

June 21, 2023

Conditions
Healthy Adult Subjects
Interventions
DRUG

CRB4101

"After the participants who signed the informed consent have been screened by the inclusion criteria, those who meet the inclusion criteria and those who do not meet the exclusion criteria will receive the following 6 dose groups in order from low to high:~100mg, 200 mg, 400 mg, 800 mg, 1200 mg, 1600 mg In each dose group, 8 participants will be enrolled to receive the drug, including 6 receiving CRB4101 tablets and 2 receiving placebo."

DRUG

Placebo

"After the participants who signed the informed consent have been screened by the inclusion criteria, those who meet the inclusion criteria and those who do not meet the exclusion criteria will receive the following 6 dose groups in order from low to high:~100mg, 200 mg, 400 mg, 800 mg, 1200 mg, 1600 mg In each dose group, 8 participants will be enrolled to receive the drug, including 6 receiving CRB4101 tablets and 2 receiving placebo."

Trial Locations (1)

000000

RECRUITING

Peking University Third Hospital, Beijing

All Listed Sponsors
collaborator

Peking University Third Hospital

OTHER

lead

China Resources Biopharmaceutical Co., Ltd

INDUSTRY