Safety and Efficacy Following Repeat-Dose of Evinacumab (Anti-ANGPTL3) in Patients With Severe Hypertriglyceridemia (sHTG) at Risk for Acute Pancreatitis
Status: | Recruiting |
---|---|
Conditions: | Gastrointestinal, Metabolic |
Therapuetic Areas: | Gastroenterology, Pharmacology / Toxicology |
Healthy: | No |
Age Range: | 18 - 75 |
Updated: | 1/17/2019 |
Start Date: | June 7, 2018 |
End Date: | January 22, 2021 |
Contact: | Clinical Trials Administrator |
Email: | clinicaltrials@regeneron.com |
Phone: | 844-734-6643 |
A Phase 2, Randomized, Placebo-Controlled Study of Safety and Efficacy, Following Repeat-Dose Administration of Evinacumab (Anti-ANGPTL3) in Patients With Severe Hypertriglyceridemia (sHTG) at Risk for Acute Pancreatitis
The primary objective is to determine the change in Triglyceride (TG) levels following 12
weeks of repeated Intravenous (IV) doses of evinacumab.
weeks of repeated Intravenous (IV) doses of evinacumab.
Key Inclusion Criteria:
1. Previous documentation in the patient's medical records of a fasting serum TG
measurement ≥ 1000 mg/dL (11.3 mmol/L) on more than 1 occasion, and all fasting TG
values ≥500 mg/dL (5.6 mmol/L) at screening
2. History of a hospitalization and diagnosis of acute pancreatitis in the past 10 years
3. On stable lipid-modifying diet with or without medications (eg, statins, niacin,
omega-3 fatty acids). Lipid-modifying diet and doses of medications should be stable
for at least 4 weeks (6 weeks for fibrates, 8 weeks for PCSK9 inhibitors) prior to
screening
4. Body mass index (BMI) of 18-40 kg/m2
Key Exclusion Criteria:
1. A hospital or clinic discharge diagnosis of acute pancreatitis within 12 weeks of
screening
2. Lipid apheresis or plasma exchange treatment within the last 4 weeks or plans to
undergo apheresis or plasma exchange during the time frame of the study
3. History of class 3/4 heart failure at any time in the past, or hospitalization for
heart failure, diagnosis of a myocardial infarction, stroke, Transient ischemic attack
(TIA), unstable angina, Coronary artery bypass surgery (CABG), Percutaneous coronary
intervention (PCI), carotid surgery/stenting within 3 months before the screening
visit
4. History of bleeding disorders, esophageal varices, heparin induced thrombocytopenia,
or contraindications to receiving heparin (eg, allergic reaction to heparin)
5. Previous treatment with Glybera® in the past 5 years or treatment with lomitapide or
mipomersen in the past 6 months
6. Pregnant or breast feeding women
Note: Other protocol defined Inclusion/Exclusion criteria may apply
We found this trial at
12
sites
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