LivingGLP1
Study S002206

A Clinical Study of Mass Balance of [14C]HRS-7535 in Healthy Adult Chinese Subjects

Registration

Registration
NCT06819488
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
6
Start
2025-02-27
Primary completion
2025-04-16
Lead sponsor
Shandong Suncadia Medicine Co., Ltd.
Conditions
Type 2 Diabetes Mellitus; Weight Loss
Interventions
DRUG:[14C]HRS-7535
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • The time of maximum observed concentration (Tmax) [0-120 hours.]
  • The maximum observed concentration (Cmax) [0-120 hours.]
  • The terminal half-life (t1/2) [0-120 hours.]
  • The total body clearance for extravascular administration (CL/F) [0-120 hours.]
  • The total radioactivity ratio for blood [0-96 hours.]
  • The total radioactivity ratio for plasma [0-96 hours.]

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