LivingGLP1
Study S003246

A Clinical Study on the Mass Balance of [14C]DA-302168S in Healthy Adult Male Trial Participants in China

Registration

Registration
NCT07857265
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
NOT_YET_RECRUITING
Enrollment
10
Start
2026-11-20
Primary completion
2026-12-20
Lead sponsor
Chendu DIAO Pharmaceutical Group CO., LTD.
Conditions
Healthy Adult Subjects
Interventions
DRUG:[14C] DA-302168S
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Total recovery of HDM1002 radioactivity in urine and feces, following oral administration of [14C] DA-302168S [Predose up to Day 8 after administration of [14C]DA-302168S]
  • Identification of Major Metabolites in Human Plasma, Urine, and Feces [Predose up to Day 8 after administration of [14C]DA-302168S]

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