Safety, Tolerability and Pharmacokinetic Characteristics Evaluation of DA-302168S Tablets

PHASE1CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

April 18, 2024

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2024

Conditions
Overweight and Obesity
Interventions
DRUG

DA-302168S

SAD study may cotain 7 cohorts at dosage of 2.5 mg, 7.5 mg, 15 mg, 30 mg, 50 mg, 75 mg, 100 mg. Each cohort enrolls 6 subjects receive DA-302168S tablets.

DRUG

Placebo of DA-302168S

SAD study may cotain 7 cohorts at dosage of 2.5 mg, 7.5 mg, 15 mg, 30 mg, 50 mg, 75 mg, 100 mg. Each cohort enrolls 2 subjects receive placebo of DA-302168S tablets.

DRUG

DA-302168S

MAD study may cotain 1-4 cohorts which were evaluated in SAD study to be tolerated . Each cohort enrolls 8 subjects receive study DA-302168S tablets.

DRUG

Placebo of DA-302168S

MAD study may cotain 1-4 cohorts which were evaluated in SAD study to be tolerated . Each cohort enrolls 2 subjects receive study placebo of DA-302168S tablets.

Trial Locations (1)

210008

Gulou Hospital Affiliated to Nanjing Medical University, Nanjing

All Listed Sponsors
lead

Chendu DIAO Pharmaceutical Group CO., LTD.

INDUSTRY

NCT06534320 - Safety, Tolerability and Pharmacokinetic Characteristics Evaluation of DA-302168S Tablets | Biotech Hunter | Biotech Hunter