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

NCT03776123 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 347

Last updated 2024-05-29

No results posted yet for this study

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

Sponsors & Collaborators

Principal Investigators

  • Ipsen Medical Director · Ipsen

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-15
Primary Completion
2024-03-26
Completion
2024-03-26

Countries

  • South Korea

Study Locations

More Related Trials

Entities

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 NCT03776123 on ClinicalTrials.gov