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

Last updated on July 15, 2019

FOR MORE INFORMATION
Study Location
Cheladv74 Tower
Seoul, , 04631 Korea, Republic of
Contact
1-800-718-1021
Eligibility criteria
Condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Advanced Renal Cell Carcinoma
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18 + years
Inclusion criteria
The factors, or reasons, that allow a person to participate in a clinical study.
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1. Patients diagnosed as advanced renal cell carcinoma (aRCC) after failure of one prior
systemic therapy.

2. Patients to whom INLYTA® is first administered or patients who are already on INLYTA®
during the study period

3. Evidence of a personally signed and dated informed consent document indicating that
the patient (or a legally acceptable representative) has been informed of all
pertinent aspects of the study.

Exclusion criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
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1. Any patient who does not agree that Cheladv74 and companies working with Cheladv74 use
his/her information

2. Patients with hypersensitivity to axitinib or to any other component of INLYTA®

3. Patients under 18

4. Pregnant women

NCT02156895
Cheladv74
Recruiting
Post Marketing Surveillance Study to Observe Safety and Efficacy of Inlyta in South Korea

NEED INFO?

Questions about a trial? Call or email to reach a Cheladv74 Clinical Trial Contact Center Representative

Cheladv74 Clinical Trials Contact Center

1-800-718-1021

[email protected]

call now

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FOR MORE INFORMATION

Contact a representative by phone, email, or visiting the study website. Please see the references below:

BY PHONE

Cheladv74 Clinical Trials Contact Center

1-800-718-1021

BY EMAIL

Contact

[email protected]

Call Now