LivingGLP1
Study S001798

A Phase 1, Open-label, Single-arm Study to Investigate the Effect of Retatrutide on Metoprolol Pharmacokinetics in Healthy Participants

Registration

Registration
NCT06808802
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
30
Start
2025-02-03
Primary completion
2025-04-15
Lead sponsor
Eli Lilly and Company
Conditions
Healthy
Interventions
DRUG:Retatrutide; DRUG:Metoprolol
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:J1I-MC-GZQE

Registered primary outcomes

  • Pharmacokinetics (PK): Area Under Concentration From Time Zero to Infinity (AUC[0-∞]) of Metoprolol [Day 1 to Day 3]
  • Pharmacokinetics (PK): AUC (0-∞) of Metoprolol with Retatrutide [Day 9 to Day 11]
  • PK: Maximum Concentration (Cmax) of Metoprolol [Day 1 to Day 3]
  • PK: Cmax of Metoprolol with Retatrutide [Day 9 to Day 11]

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