LivingGLP1
Study S000024

A Single-center, Open-label, Phase Ⅰ Clinical Study of the Absorption, Metabolism, and Excretion of [14C]HRS9531 in Healthy Male Subjects

Registration

Registration
NCT06855147
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
7
Start
2025-04-21
Primary completion
2025-06-17
Lead sponsor
Fujian Shengdi Pharmaceutical Co., Ltd.
Conditions
Type 2 Diabetes Mellitus; Weight Loss
Interventions
DRUG:[14C]HRS9531
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • Maximum concentration (Cmax). [0 to anticipated 64 days.]
  • Time to reach the maximum concentration (Tmax). [0 to anticipated 64 days.]
  • Half-life (t1/2). [0 to anticipated 64 days.]
  • Total radioactive recovery rate in urine. [0 to anticipated 64 days.]
  • Total radioactive recovery rate in feces. [0 to anticipated 64 days.]
  • Cumulative radioactive recovery rate in urine. [0 to anticipated 64 days.]
  • Cumulative radioactive recovery rate in feces. [0 to anticipated 64 days.]

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