A Study to Evaluate the Pharmacokinetics,Safety and Tolerability of Y-2 Sublingual Tablet in Healthy Adult Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

September 6, 2023

Primary Completion Date

November 21, 2023

Study Completion Date

December 5, 2023

Conditions
Healthy
Interventions
DRUG

Y-2 Sublingual Tablet

Subjects will receive one Y-2 sublingual tablet sublingually once daily for Day1 and Day 19 and twice daily for Day 6 to Day 18.

DRUG

Y-2 Sublingual Tablet

Subjects will receive two Y-2 sublingual tablets sublingually once daily for Day1 and Day 19 and twice daily for Day 6 to Day 18.

DRUG

Y-2 Sublingual Tablet

Subjects will receive Y-2 sublingual tablet with 3 different conditions once daily for Day1 Day 6 and Day 11. Day 1 with condition A, Day 6 with condition B and Day 11 with condition C.

DRUG

Y-2 Sublingual Tablet

Subjects will receive Y-2 sublingual tablet with 3 different conditions once daily for Day1 Day 6 and Day 11. Day 1 with condition B, Day 6 with condition C and Day 11 with condition A.

DRUG

Y-2 Sublingual Tablet

Subjects will receive Y-2 sublingual tablet with 3 different conditions once daily for Day1 Day 6 and Day 11. Day 1 with condition C, Day 6 with condition A and Day 11 with condition B.

DRUG

Placebo

Placebo, sublingually, single and multiple ascending dosing in group 1 and 2 subjects.

Trial Locations (1)

91206

Parexel International Los Angeles Early Phase Clinical Unit, Glendale

All Listed Sponsors
lead

Simcere Pharmaceutical Co., Ltd

OTHER

NCT05940883 - A Study to Evaluate the Pharmacokinetics,Safety and Tolerability of Y-2 Sublingual Tablet in Healthy Adult Subjects | Biotech Hunter | Biotech Hunter