CAPIVASERTIB REGULATORY POSTMARKETING SURVEILLANCE IN KOREA
NCT06927648 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 130
Last updated 2026-05-19
Summary
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.
Conditions
Sponsors & Collaborators
- lead INDUSTRY
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-10-15
- Primary Completion
- 2029-12-30
- Completion
- 2029-12-30
Countries
- South Korea
Study Locations
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