Post-marketing Surveillance of Linaclotide Tablet in Patients With Irritable Bowel Syndrome With Constipation or Chronic Constipation (Excluding Constipation Due to Organic Diseases)

NCT03471728 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2475

Last updated 2024-10-18

No results posted yet for this study

Summary

The objective of this study is to evaluate the long-term safety and efficacy of linaclotide in post-marketing use.

Conditions

  • Chronic Constipation (CC) (Excluding Constipation Due to Organic Diseases)
  • Irritable Bowel Syndrome With Constipation (IBS-C)

Interventions

DRUG

linaclotide

Oral

Sponsors & Collaborators

  • Astellas Pharma Inc

    lead INDUSTRY

Principal Investigators

  • Central Contact · Astellas Pharma Inc

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-02
Primary Completion
2021-12-31
Completion
2021-12-31

Countries

  • Japan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03471728 on ClinicalTrials.gov