Recruiting

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The first group needed to complete a single-dose clinical study at a dose of 2 mg and 10 subjects, 8 of whom received the test drug and 2 received placebo, with a similar male-to-female ratio. Administered once, administered under fasting conditions, and tolerated at D4. ;A second set of tests was performed on the first set of tolerability evaluations. The second group needed to complete a single-dose clinical study at a dose of 5 mg with 10 subjects, 8 of whom received the test drug and 2 received placebo, with a similar male-to-female ratio. Administered once, ;The third set of tests was conducted with the second set of tolerability evaluable as tolerated. The third group needed to complete a single-dose clinical study at a dose of 10 mg with 10 subjects, 8 of whom received the investigational drug, 2 received placebo, and the ratio of men and women ;A fourth set of tests was conducted with the third set of tolerability evaluable as tolerated. The fourth group dose of 20mg, need to complete a single administration, the impact of food on pharmacokinetics, multiple clinical trials and drug metabolism research, a total of 18 subjects, A group of 10 ;The fifth set of tests was conducted with the fourth set of tolerability evaluable as tolerated. The fifth group needed to complete a single-dose clinical study at a dose of 40 mg with 10 subjects, 8 of whom received the test drug and 2 received placebo, with a similar male-to-female ratio. Admi ;A sixth set of tests was conducted with the fifth set of tolerability evaluable as tolerated. The sixth group needed to complete a single-dose clinical study at a dose of 40 mg in 10 subjects, 8 of whom received the test drug and 2 received placebo, with a similar male-to-female ratio. Administe ;First selected 2 subjects participated in the 2mg TQ-F3083 single-dose pre-trial clinical study

The First Hospital of Jilin University; Chia Tai Tianqing Pharmaceutical Group Co, Ltd, Chia Tai Tianqing Pharmaceutical Group Co,Ltd

Diabetes