TrialSignal
Clinical trial intelligence report
A Study to Evaluate Tirzepatide Concentrations in Breastmilk Following Administration of Single Dose of Tirzepatide by Subcutaneous Injection in Healthy Lactating Females
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 16, 2026
NCT ID
NCT05978713
Status
COMPLETED
Phase
Phase 1
Sponsor
Eli Lilly and Company
Executive brief
Investment-Ready Snapshot
Tirzepatide, developed by Eli Lilly and Company, is positioned as a dual agonist targeting GLP-1 and GIP receptors, primarily indicated for the treatment of obesity and type 2 diabetes. The current study focuses on its pharmacokinetics in breastmilk, which could have implications for its use in lactating women. The completion of this study may enhance the product's marketability by addressing safety concerns in breastfeeding populations, potentially expanding its user base. Competitive analysis indicates that while tirzepatide faces competition from other GLP-1 receptor agonists, its unique dual-action mechanism may provide a distinct advantage. Diligence considerations should include ongoing monitoring of safety profiles and market acceptance in lactating demographics.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05978713
Indication
Healthy
Modality
small molecule
Target
GLP-1 receptor and GIP receptor agonist
Intervention
Tirzepatide
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.