Condition: Endometriosis · Sponsor: Kissei Pharmaceutical Co., Ltd.
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-back hormone replacement therapy (ABT: estradiol (E2) 1 mg / norethisterone acetate (NETA) 0.5 mg) versus placebo, in the management of moderate to severe endometriosis-associated pain (EAP).
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Birmingham OBGYN / ID # 740 | Birmingham, Alabama, United States | — |
| Mesa Obstetricians and Gyneocologists / ID # 790 | Mesa, Arizona, United States | — |
| Precision Trials AZ, LLC / ID # 783 | Phoenix, Arizona, United States | — |
| Quality of LIfe Medical & Research Center, LLC / ID # 813 | Tucson, Arizona, United States | — |
| Visions Clinical Research-Tucson / ID # 754 | Tucson, Arizona, United States | — |
| Lynn Institute of the Ozarks / ID # 826 | Little Rock, Arkansas, United States | — |
| Applied Research Center of Arkansas / ID # 735 | Little Rock, Arkansas, United States | — |
| Join Clinical Trials / ID # 778 | Huntington Park, California, United States | — |
| Long Beach Clinical Trials, LLC / ID # 768 | Long Beach, California, United States | — |
| Matrix Clinical Research / ID # 751 | Los Angeles, California, United States | — |
| Futura Research, Org / ID # 781 | Norwalk, California, United States | — |
| National Research Institute / ID # 805 | Panorama City, California, United States | — |
+ 100 more locations — full list on the registry record.
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