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CompletedNCT03776123

Post-marketing Surveillance on the Safety of CabometyxTM in Korean Patients

Post-marketing Surveillance on the Safety of CabometyxTM in Korean Patients Based on "Guideline for Re-examination of New Drugs"

Status
Completed
Phase
Study type
Observational
Enrollment
347 (actual)
Sponsor
Ipsen · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The objective of this Post Marketing Surveillance (PMS) is to collect and describe safety and effectiveness profile of Cabometyx™ in real clinical practice setting, according to the approved labelling after the approval of marketing authorization.

Conditions

Timeline

Start date
2019-05-15
Primary completion
2024-03-26
Completion
2024-03-26
First posted
2018-12-14
Last updated
2024-05-29

Locations

47 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03776123. Inclusion in this directory is not an endorsement.

Post-marketing Surveillance on the Safety of CabometyxTM in Korean Patients (NCT03776123) · Clinical Trials Directory