Real-World Treatment Study of Koselugo (Selumetinib)

Status: Recruiting
Location: See all (12) locations...
Study Type: Observational
SUMMARY

As part of a post-approval commitment, the Korean health authority requests a study to characterize safety and effectiveness in patients treated with Koselugo (Selumetinib), an oral selective inhibitor of MAPK kinase (MEK) 1 and 2, by physicians in routine clinical practice settings. This study is designed to assess the known safety profile or identify previously unsuspected adverse reactions and evaluate the effectiveness of Koselugo under conditions of routine daily medical practice in Korea. This study will provide information on the Korean patient population that is treated with the study drug.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 18
Healthy Volunteers: f
View:

• Patients treated with Koselugo (Selumetinib) under the approved label in South Korea

• Provision of signed and dated written informed consent by the patient or legally acceptable representative

Locations
Other Locations
Republic of Korea
Research Site
RECRUITING
Busan
Research Site
RECRUITING
Chungcheongbuk-do
Research Site
RECRUITING
Daejeon
Research Site
RECRUITING
Gyeonggi-do
Research Site
RECRUITING
Incheon
Research Site
RECRUITING
Jeonnam
Research Site
NOT_YET_RECRUITING
Seoul
Research Site
RECRUITING
Seoul
Research Site
COMPLETED
Seoul
Research Site
SUSPENDED
Seoul
Research Site
RECRUITING
Wŏnju
Research Site
RECRUITING
Yangsan
Contact Information
Primary
AstraZeneca Clinical Study Information Center
information.center@astrazeneca.com
1-877-240-9479
Time Frame
Start Date: 2024-06-15
Estimated Completion Date: 2031-09-30
Participants
Target number of participants: 150
Sponsors
Leads: AstraZeneca

This content was sourced from clinicaltrials.gov