Antiphospholipid Syndrome (APS) ACTION Plaquenil
Status: | Recruiting |
---|---|
Conditions: | Cardiology, Endocrine |
Therapuetic Areas: | Cardiology / Vascular Diseases, Endocrinology |
Healthy: | No |
Age Range: | 18 - 60 |
Updated: | 2/20/2016 |
Start Date: | April 2015 |
End Date: | March 2017 |
Contact: | Tania Moin |
Email: | moint01@nyumc.org |
A Multicenter International Prospective, Randomized Controlled Trial of Hydroxychloroquine in the Primary Thrombosis Prophylaxis of Persistently Antiphospholipid Antibody (aPL) Positive But Thrombosis-free Patients Without Systemic Autoimmune Diseases.
The primary objective of this phase III study is to determine the efficacy of
Hydroxychloroquine in the primary thrombosis prevention of persistently Antiphospholipid
Antibody-(aPL)-positive but thrombosis free patients with no other systemic autoimmune
diseases over the five year study period. Additionally, investigators are looking to
determine thrombosis incident rate, the effect of Hydroxychloroquine on mortality rate and
effect of Hydroxychloroquine on antiphospholipid antibodies (aPL) profile.
Hydroxychloroquine in the primary thrombosis prevention of persistently Antiphospholipid
Antibody-(aPL)-positive but thrombosis free patients with no other systemic autoimmune
diseases over the five year study period. Additionally, investigators are looking to
determine thrombosis incident rate, the effect of Hydroxychloroquine on mortality rate and
effect of Hydroxychloroquine on antiphospholipid antibodies (aPL) profile.
Based on the randomization, patients will be assigned to receive Hydroxychloroquine or no
treatment in addition to their standard regimen. Hydroxychloroquine dose will be
weight-adjusted: 200 mg daily for patients weighing < 60kg; and 400 mg daily (200 mg twice a
day) for patients weighing > 60kg. Hydroxychloroquine tablets will be dispensed by the study
site's pharmacy. The patient compliance will be documented by the pill counts during study
visits that will be completed every 6 months. Patients will be aware of the
hydroxychloroquine doses that they will receive.
treatment in addition to their standard regimen. Hydroxychloroquine dose will be
weight-adjusted: 200 mg daily for patients weighing < 60kg; and 400 mg daily (200 mg twice a
day) for patients weighing > 60kg. Hydroxychloroquine tablets will be dispensed by the study
site's pharmacy. The patient compliance will be documented by the pill counts during study
visits that will be completed every 6 months. Patients will be aware of the
hydroxychloroquine doses that they will receive.
Inclusion Criteria:
- Age 18-60
- Persistent (at least 12 weeks apart) aPL-positivity within 12 months prior to the
screening defined as:
- aCL IgG/M (> 40U, medium-to-high titer, and/or greater than the 99th percentile)
and/or
- aβ2GPI IgG/M (>40U, medium-to-high titer, and/or greater than the 99th percentile)
and/or
- Positive LA test based on the International Society of Thrombosis & Haematosis
Recommendations
Exclusion Criteria:
- History of thrombosis (arterial, venous, and/or biopsy proven microthrombosis)
- Of note, history of superficial thrombophlebitis is not an exclusion criterion.
- History of Transient Ischemic Attack Confirmed by a Neurologist
- SLE Diagnosis based on the ACR Classification Criteria > 4/11
- Other Systemic Autoimmune Diseases diagnosed based on ACR Classification Criteria
(e.g., RA, Systemic Vasculitis, Spondylarthropathy, Systemic Sclerosis, Inflammatory
Muscle Disease, Sjogren Syndrome, Mixed Connective Tissue Disorder)
- Current HCQ or another antimalarial treatment (-3 months)
- Current warfarin treatment (- 3 months)
- Current heparin therapy (- 3 months)
- Current pregnancy
- Acute seizure within 7 days prior to screening (contraindication for HCQ treatment)
- Psoriasis (contraindication for HCQ treatment)
- History of HCQ eye toxicity
- History of Hydroxychloroquine allergy
- Liver disease with AST or ALT two times of the upper limit
- Known glucose-6-phosphate dehydrogenase deficiency
- Known malignancy (with the exception of non-metastatic squamous cell and basal cell
skin carcinomas)
- Alcoholism (chronic alcohol abuse)
- Known illicit drug abuse
- Patient refusal
- Inability to comply with study and follow-up procedures
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