Study of LJP 394 (Abetimus Sodium) in Lupus Patients
NCT00390091 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2015-09-01
Summary
The primary purpose of this study is to assess the safety and pharmacodynamic effect of LJP 394 at doses of 100 mg, 300 mg and 900 mg on anti-dsDNA antibody levels in patients with SLE.
Conditions
Interventions
- DRUG
-
abetimus sodium (LJP 394)
Sponsors & Collaborators
-
La Jolla Pharmaceutical Company
lead INDUSTRY
Principal Investigators
-
Matthew D Linnik, PhD · La Jolla Pharmaceutical Company
Study Design
- Allocation
- RANDOMIZED
- Purpose
- DIAGNOSTIC
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2006-09-30
Countries
- United States
Study Locations
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