Condition: Cardiovascular Disease With Mention of Arteriosclerosis · Elevated Cholesterol · Familial Hypercholesterolemia · Sponsor: LIB Therapeutics LLC
The study is to assess the long-term safety, tolerability, and efficacy after 48 and 72 weeks with monthly (Q4W \[\<31 days\]) dosing of subcutaneous (SC) LIB003 300 mg administered in patients with CVD or at high risk for CVD (including HoFH and HeFH) on stable diet and oral LDL-C lowering drug therapy who completed one of the LIB003 Phase 3 base studies.
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.
| NorthShore University Health System | Evanston, Illinois, United States | — |
| Sterling Research Group | Cincinnati, Ohio, United States | — |
| The Lindner Research Center | Cincinnati, Ohio, United States | — |
| Metabolic & Atherosclerosis Research Center (MARC) | Cincinnati, Ohio, United States | — |
| G.B. Pant Institute of Postgraduate Medical Education & Research | New Delhi, India | — |
| Department of Medicine, Hadassah University Hospital | Jerusalem, Israel | — |
| Rabin Medical Center, Beilinson Hospital, | Petah Tikva, Israel | — |
| Lipid Clinic, Oslo University Hospital | Oslo, Norway | — |
| Carbohydrate and Lipid Metabolism Research Unit | Johannesburg, Gauteng, South Africa | — |
| Division of Lipidology, Department of Medicine University of Cape Town | Cape Town, Western Province, South Africa | — |
| Ege University Medical School | Izmir, Bornova, Turkey (Türkiye) | — |
| Afyonkarahisar Health Sciences University | Afyonkarahisar, Turkey (Türkiye) | — |
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