| 靶点- | 
| 作用机制- | 
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|  | 
|  | 
| 非在研适应症- | 
| 最高研发阶段临床1期 | 
| 首次获批国家/地区- | 
| 首次获批日期- | 
| 靶点- | 
| 作用机制- | 
|  | 
|  | 
|  | 
| 非在研适应症- | 
| 最高研发阶段临床前 | 
| 首次获批国家/地区- | 
| 首次获批日期- | 
A Phase 1, Randomized, Double-blind, Placebo Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ART101 in Adult Participants With Hypertension.
This is a Phase 1, first-in-human, randomized, double-blind, placebo-controlled, study to assess the safety, tolerability, Pharmacokinetics (PK), and pharmacodynamics (PD) of a single dose of ART101 administered via subcutaneous injection to hypertensive adult participants. An anticipated 5 dose cohorts (one as optional) with maximum of 40 participants will be randomized in SAD study.
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