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Special Investigation for LORBRENA Tablets
To investigate the following matters under post-marketing use of Lorbrena in patients who received this drug 1. Factors affecting the onset of central nervous system disorder 2. Effect of Lorbrena in combination with CYP3A inducers on the onset of hepatic dysfunction
Age
0 - No limit years
Sex
ALL
Healthy Volunteers
No
3-22-7, Yoyogi, Shibuya-ku
Tokyo, Japan
Start Date
January 21, 2019
Primary Completion Date
July 30, 2025
Completion Date
July 30, 2025
Last Updated
September 4, 2025
1,290
ACTUAL participants
Lead Sponsor
Pfizer
NCT06305754
NCT07190248
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07100080