Study of ISIS 678354 (AKCEA-APOCIII-LRx) in Patients With Hypertriglyceridemia and Established Cardiovascular Disease (CVD)
Status: | Recruiting |
---|---|
Conditions: | High Cholesterol, Peripheral Vascular Disease, Metabolic |
Therapuetic Areas: | Cardiology / Vascular Diseases, Pharmacology / Toxicology |
Healthy: | No |
Age Range: | 18 - 80 |
Updated: | 12/15/2018 |
Start Date: | January 5, 2018 |
End Date: | May 31, 2019 |
Contact: | Akcea Therapeutics |
Email: | cjensen@akceatx.com |
Phone: | 617-207-0297 |
A Randomized, Double-blind, Placebo-Controlled, Dose-Ranging Phase 2 Study of ISIS 678354 Administered Subcutaneously to Patients With Hypertriglyceridemia and Established Cardiovascular Disease (CVD)
This is a multicenter, randomized, double-blind, placebo-controlled, dose-ranging study to
evaluate the safety, including tolerability, of ISIS 678354 and to assess the efficacy of
different doses and dosing regimens of ISIS 678354 for reduction of serum triglyceride (TG)
levels in patients with hypertriglyceridemia and established CVD.
evaluate the safety, including tolerability, of ISIS 678354 and to assess the efficacy of
different doses and dosing regimens of ISIS 678354 for reduction of serum triglyceride (TG)
levels in patients with hypertriglyceridemia and established CVD.
Key Inclusion Criteria:
- Clinical diagnosis of CVD (defined as documented coronary artery disease, stroke, or
peripheral artery disease
- Fasting serum TG ≥ 200 mg/dL (≥ 2.3 mmol/L) and ≤ 500 mg/dL (≥ 5.7 mmol/L) at
Screening.
- Fasting TG ≥ 200 mg/dL and ≤ 500 mg/dL at Qualification visit.
- Must be on standard-of-care preventative therapy for known CVD risk factors
Key Exclusion Criteria:
- Within 6 months of Screening: acute coronary syndrome, major cardiac surgery, or
stroke/TIA
- Within 3 months of Screening: coronary, carotid, or peripheral arterial
revascularization, major non-cardiac surgery, or lipoprotein apheresis
- Heart failure New York Heart Association (NYHA) class IV
- Type 1 diabetes mellitus
- Type 2 diabetes mellitus with any of the following:
- Newly diagnosed within 12 weeks of screening
- HbA1c ≥ 9.0% at Screening
- Recent change in anti-diabetic pharmacotherapy (change in dosage or addition of
new medication within 12 weeks of screening [with the exception of ± 10 units of
insulin
- BMI > 40 kg/m2
We found this trial at
25
sites
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