Apixaban in Thrombocytopenia
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Rushad Patell
- Study ID
- NCT06886516
- Phase
- EARLY_PHASE1
- Status
- Recruiting
Conditions
- Deep Vein Thrombosis
- Pulmonary Embolism and Thrombosis
- Recurrent Venous Thromboembolism
- Thrombocytopenia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Apixaban — DRUGA factor Xa inhibitor, 2.5 and 5 mg tablets, by mouth per protocol.
Study Details
This study is being done to determine the feasibility and safety of using a novel dose adjusted apixaban for the management of participants with cancer-associated venous thromboembolism (blood clot) or and thrombocytopenia (low number of platelets in the blood). Investigators are also looking to see if participants on this treatment have fewer bleeding episodes. The name of the study drug involved in this study is: -Apixiban (a type of anticoagulant)
Key Dates
- Start date
- Feb 28, 2025
- Status verified
- Apr 2026
- Primary completion
- Jul 1, 2027
- Completion
- Jul 1, 2029
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: DOSE-ADJUSTED APIXABAN30 enrolled participants will complete study procedures as follows: * Baseline visit with assessments * Predetermined dose of Apixiban 2x daily for 90 days * Off treatment visit 7 days after last study drug dose * Follow up visit 6 weeks after last study drug dose
Primary Outcome Measure
Study Enrollment [ Time Frame: Up to 5 years ]
Central Contacts
- Rushad Patell, MD617-667-9179
- Fernanda De Queiroz Silva, MD617-667-9920
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | 02215 | Rushad Patell, MD (PRINCIPAL_INVESTIGATOR) |
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