LivingGLP1
Study S000212

A Phase 1, Randomized, Double-blind, Multiple-dose Study to Evaluate the Pharmacokinetics of AMG 133 Administered Subcutaneously in Subjects With Overweight or Obesity

Registration

Registration
NCT06976372
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
120
Start
2024-08-20
Primary completion
2024-12-27
Lead sponsor
Amgen
Conditions
Overweight; Obesity
Interventions
DRUG:AMG 133
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • Maximum Concentration (Cmax) of AMG 133 [Up to Day 99]
  • Area Under the Plasma Concentration-time Curve from Time Zero to the Last Quantifiable Concentration (AUClast) of AMG 133 [Day 29]
  • Area Under the Plasma Concentration-time Curve from Time Zero to Infinity (AUCinf) of AMG 133 [Day 29]
  • Area Under the Plasma Concentration-time Curve Over the Dosing Interval (AUCtau) of AMG 133 [Day 1 and Day 15]

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