The Assessment of Single-Dose Safety,Tolerability, Pharmacokinetics and Pharmacodynamic of Globalagliatin Hydrochloride

• Status: Completed
• Trial end date: 2018-01-09
• Target enrollment: 0
• Participant gender: All

Summary

This is a phase 1 randomized,double-blind,placebo-controlled study with single oral dose of globalagliatin hydrochloride (SY-004) administered to chinese healthy subjects to evaluated the safety, tolerability, pharmacokinetics and pharmacodynamics of globalagliatin hydrochloride (SY-004).

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Yabao Pharmaceutical Group

Criteria

Inclusion Criteria:

• males and females between the ages of 18 and 65 years, inclusive, healthy subjects

• A screening body mass index (BMI) of 18 to 26 kg/m2 inclusive, body weight above 50kg

• FPG≥3.9mmol/L and <6.1 mmol/L

• Have medical history, physical examination, laboratory tests and other relative test results within the normal range or with abnormalities deemed clinically insignificant by the investigator.

• Have given written informed consent.

• The subjects took effective contraceptive measures, and had no birth plan within 3 months.Female subjects should be non lactating, negative pregnancy test, or no fertility potential (Women who were 12 months of menopause or without uterus were found to have no potential for pregnancy )

Exclusion Criteria:

• There is a serious history of systemic disease, or a family history (including cardiovascular system, digestive system, urinary system, etc.)

• Have taken a special diet or exercise before 48 hours of drug administration or other factors are capable of significantly altering the absorption, or metabolism or elimination of drugs.

• A significant abnormality in ALT,AST or other lab test results

• Frontal chest X light result is clinical significantly abnormal.

• Have known intolerance of or allergies to glucokinase activators, or related compounds.

• Have known allergies to other compounds or biologic products.

• Have a major surgery in the last 4 weeks before dosing.

• To inoculate any live vaccine within 4 weeks before drug administration.

• Have a history of drug abuse

• Use any prescription drugs within 4 weeks prior to administration or use OTC or traditional Chinese medicine within 1 weeks before enrollment.

• Regular drinkers within 6 months before or during the trial (Subjects who have an average weekly alcohol intake that exceeds 21 units per week (males) and 14 units per week (females) [1 unit = 360 mL of beer; or 150 mL of wine; or 45 mL of distilled spirits])

• The amount of daily cigarette smoking was more than 5/day in last 3 months, or subjects unwilling to stop cigarette consumption during the trial.

• Are enrolled in 4 or more clinical trials within last year, or participated any clinical trail within 3 months before enrollment ; plan to donate blood or blood donation of 450 mL or more in the last 3 months; or have blood transfusion 4 weeks before the trial.

• An clinical significant abnormality in the 12-lead ECG at screening or baseline: QT interval> 450 ms

• Subjects deemed unsuitable by the Investigator for low compliance or any other reason.

• investigator and their immediate families.