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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1800-01-20 |
一项评价DR10624单次和多次皮下给药、剂量递增的安全性、耐受性、药代动力学和药效学的随机、安慰剂对照、双盲、Ⅰ期研究
在中国健康成人受试者、超重或肥胖受试者中评估DR10624单次皮下给药的安全性和耐受性。
A Phase 1, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single-and-Multiple-Ascending Subcutaneous Doses of DR10624
DR10624 is an Fc fusion protein tri-agonist with balanced glucagon-like peptide-1 receptor (GLP-1R)/glucagon receptor (GCGR)/ fibroblast growth factor 21 receptor (FGF21R) agonizing activities. The objectives of the planned clinical investigation will be to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single- and multiple-ascending doses of DR10624 via subcutaneous (SubQ) injection in a randomized, placebo-controlled, double-blind study.
100 项与 GCGR x GLP-1R x FGF21R 相关的临床结果
100 项与 GCGR x GLP-1R x FGF21R 相关的转化医学
0 项与 GCGR x GLP-1R x FGF21R 相关的专利(医药)