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The primary objective of this study is to demonstrate the efficacy and safety of linzagolix administered orally once daily for 3 months at a dose of 75 mg alone or of 200 mg in combination with add-ba...
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Lead Sponsor
Kissei Pharmaceutical Co., Ltd.
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Achieve Clinical Research/ ID # 601
Birmingham, Alabama
Choice Research, LLC/ ID # 609
Dothan, Alabama
Southeast Clinical Research/ ID # 618
Chiefland, Florida
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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.
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