Apixaban in Patients With Sickle Cell Disease

Phase 3

Terminated

Conditions: Sickle Cell Disease
Vaso-occlusive Crisis
Reduction in Hospitalizations

Interventions: Drug: Placebo
Drug: Apixaban

Registration Number: NCT02179177

Lead Sponsor: Nirmish Shah

Brief Summary: In patients with SCD, the use of low dose anticoagulation as an outpatient may lead to a significant decrease in morbidity and as a result, decrease healthcare utilization and costs. This study attempts to critically avoid admissions by reducing daily pain scores and pain crisis as an outpatient by use of a novel oral anticoagulant.

Detailed Description: There is not only significant morbidity associated with patients with SCD, but also costs associated with the numerous hospitalizations. Small studies have been unable to show clear benefit of the use of low dose anticoagulation in SCD due to limited sample size or the inclusion of very specific populations. However, studies have shown a decrease in the level of elevated prothrombotic markers with anticoagulation, and one study using full dose anticoagulation in patients with a generally milder form of SCD (with high protective hemoglobin) showed more rapid decrease in clinical pain with use of anticoagulation, suggesting a possible benefit of such therapy. Due to the paucity of data to support therapeutic dose LMWH in the more severe forms of SCD seen in the United States, we have chosen prophylactic dose anticoagulation. This study proposal attempts to critically avoid admissions by reducing daily pain scores and pain crisis as an outpatient by use of a novel oral anticoagulant.

The development of novel anticoagulants such as oral direct factor Xa (FXa) inhibitors allows the realistic use of daily prophylactic dosing as an outpatient. Past studies as detailed earlier have been limited by attempts to use subcutaneous injections or frequent, close monitoring for acenocoumarol treatment, both which are not ideal for chronic daily use. Furthermore, the use of global assays such calibrated automated thrombography (CAT) have shown further details about thrombin generation in a population which is hypercoagulable at baseline.

This is a double blind, parallel group, placebo controlled feasibility study with an enrollment target of 25 patients (12 per arm). All subjects that meet inclusion criteria as an outpatient, following a 1 month observation, will be randomized to receive an oral prophylactic dose factor Xa inhibitor (Apixaban 2.5mg po bid) or placebo for 6 months. Subjects will return for a 30 day (+/- 5 days) follow-up visit after the End of Treatment (EOT) visit. Initial randomization will occur by computerized randomization technique by the investigational drug services (IDS) at Duke University Medical Center.

Recruitment & Eligibility

Status: TERMINATED

Sex: All

Target Recruitment: 16

Inclusion Criteria

documented HgbSS, SC or HgbS-beta0 thalassemia,
age ≥18 years old and ≤80,
seen in outpatient clinic ≥2 times in past year
seen for an acute care visit (hospitalization, emergency department, or day hospital visit) for pain >2 times in the past year.

Exclusion Criteria

Hospitalization or day hospital visit for pain crisis within the past 2 weeks
Patients with ≥10 acute care visits within the past year will be excluded
Creatinine >3.0 mg/dL
creatinine ≥1.5 mg/dL AND weight ≤60 kg
chronic use of antiplatelet or anticoagulation medication
Patients with known vasculopathy or Moya-Moya
platelet count <100 X 109/L
AST or ALT >3 times normal
chronic red blood cell transfusions (scheduled transfusions)
packed red blood cell transfusion within the past 2 months
Use of CYP3A4 and P-gp inhibitor medications

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	Sugar pills that look like Apixaban that will be taken by mouth twice a day
Apixaban	Apixaban	Active drug Apixaban 2.5mg taken by mouth twice a day

Primary Outcome Measures

Name	Time	Method
Change in Pain as Measured by Visual Analog Scale (VAS)	Month 1 to Month 8	The primary pain assessment tool will be a 10-cm horizontal visual analog scale (VAS), with "0" corresponding to no pain at one end and "10" indicating the worst pain at the other.

Secondary Outcome Measures

Name	Time	Method
Daily Pain Scores While Hospitalized as Measured by VAS	up to 8 months	The primary pain assessment tool will be a 10-cm horizontal visual analog scale (VAS), with "0" corresponding to no pain at one end and "10" indicating the worst pain at the other. Secondary analysis will be performed to evaluate differences when patients are hospitalized and on study drug versus placebo.
Change in Thrombin Generation Using D-dimer Measurement as a Surrogate	Enrollment to 2 months
Number of Hospitalizations During Treatment	up to 8 months