Post Marketing Surveillance Study to Observe Safety and Efficacy of Inlyta in South Korea

NCT02156895 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 111

Last updated 2024-03-08

Study results available
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Summary

The objective of this study is to monitor the usage of INLYTA® in real practice, including the adverse events associated with INLYTA®.

Conditions

  • Advanced Renal Cell Carcinoma

Interventions

DRUG

Axitinib

based on Axitinib approval

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-17
Primary Completion
2021-04-21
Completion
2021-08-06

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Companies

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 NCT02156895 on ClinicalTrials.gov