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A Lactation Study in Women Who Are Breastfeeding or Pumping and Are Receiving Linaclotide Therapeutically — LIN-PK-01  

Irritable Bowel Syndrome Clinical Trial

Official title:
An Open-label, Multiple-dose, Milk-only Lactation Study in Lactating Women Receiving Linaclotide Therapeutically

Clinical Trial Summary

The purpose of this study is to determine the amount of linaclotide and its active metabolite (MM-419447) excreted in breast milk after multiple, once daily doses of linaclotide (72 μg, 145 μg, or 290 μg) in lactating women receiving the drug therapeutically.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02220348
Study type Interventional
Source Forest Laboratories
Contact
Status Completed
Phase Phase 1
Start date July 31, 2014
Completion date May 31, 2019
View Details
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