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CAPIVASERTIB REGULATORY POSTMARKETING SURVEILLANCE IN KOREA

RecruitingN/A

Sponsor: AstraZeneca

Conditions: Breast Cancer

Countries: South Korea

To fulfil the post-approval commitment of MFDS to conduct post-marketing surveillance, this study is designed to assess the known safety profile, identify previously unsuspected adverse reactions and to evaluate the effectiveness of Capivasertib under conditions of routine daily medical practice in Korea.

Eligibility overview

Sex: ALL

Age: 19 Years to —

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* Patients eligible for and treated with the study drug according to the approved label in South Korea
* Patients who provide signed and dated written informed consent, either personally or through a legally acceptable representative.

Exclusion Criteria:

* Participation in any interventional trial during the treatment of the study drug
* Other off-label indications according to the approved label in South Korea

Locations (17)

Busan, South Korea
Busan, South Korea
Busan, South Korea
Daejeon, South Korea
Daejeon, South Korea
Goyang-si, South Korea
Goyang-si, South Korea
Guri-si, South Korea
Incheon, South Korea
Incheon, South Korea
Seongnam-si, South Korea
Seoul, South Korea
Seoul, South Korea
Seoul, South Korea
Seoul, South Korea
Suwon, South Korea
Uijeongbu-si, South Korea