Drug Utilisation of Mysimba/Contrave

NCT06089824 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 43324

Last updated 2023-10-18

No results posted yet for this study

Summary

This study will assess a retrospective cohort of users of Mysimba/Contrave with up to 548 days (\~18 months) after initiation with treatment with Mysimba/Contrave. This study will describe Mysimba/Contrave utilisation and incidence of AESIs for users compliant and non-compliant with the SmPC.

Conditions

Sponsors & Collaborators

  • Currax Pharmaceuticals

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2022-10-31
Completion
2022-10-31

Countries

  • United States

Study Locations

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Entities

Diseases

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 NCT06089824 on ClinicalTrials.gov