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Double Blind, Placebo-Controlled, Dose-Escalation, Phase 1 Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Doses of ISIS 353512 Administered Intravenously and Subcutaneously to Healthy Volunteers
The purpose of this study is to evaluate the safety and tolerability of single and multiple doses of ISIS 353512, to evaluate the blood concentration and rate elimination of ISIS 353512 from the blood, and to evaluate the effectiveness of ISIS 353512 in lowering a protein in the blood associated with inflammation.
Details
| Lead sponsor | Ionis Pharmaceuticals, Inc. |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 103 |
| Start date | 2008-07 |
| Completion | 2010-03 |
Conditions
- Inflammatory Diseases
Interventions
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
- ISIS 353512
Primary outcomes
- To evaluate the safety and tolerability of single and multiple doses of ISIS 353512 administered intravenously and subcutaneously. — 14 Days post treatment of each cohort
Countries
Canada