Table 5

Recently completed and ongoing studies involving antiplatelet agents

Study titleClinical trials #/PhaseInterventionStatusPrimary sponsor
Abciximab (ReoPro) as a Therapeutic Intervention for Sickle Cell Vaso-Occlusive Pain Crisis NCT01932554 Phase 2 Abciximab Withdrawn St. Louis Univ. 
Dipyridamole/Magnesium To Improve Sickle Cell Hydration NCT00276146 Phase 2 Dipyridamole, Magnesium Withdrawn Children's Hospital Medical Center, Cincinnati 
A Phase I/II Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety of Eptifibatide as Treatment of Acute Pain Episodes in Sickle Cell Disease NCT00834899 Phase 1, 2 Eptifibatide Terminated Univ. of North Carolina-Chapel Hill 
An Assessment of Prasugrel on Healthy Adults and Sickle Cell Adults NCT01178099 Phase 1 Prasugrel Completed Ely Lilly 
A Study of Prasugrel in Pediatric Participants With Sickle Cell Disease NCT01476696 Phase 2 Prasugrel Completed Ely Lilly 
Prasugrel Versus Placebo in Adult Sickle Cell Disease NCT01167023 Phase 2 Prasugrel Completed Ely Lilly 
A Phase 3, Double-Blind, Randomized, Efficacy and Safety Comparison of Prasugrel and Placebo in Pediatric Patients With Sickle Cell Disease. NCT01794000 Phase 3 Prasugrel Active, not recruiting Eli Lilly 
Aspirin Prophylaxis in Sickle Cell Disease NCT00178464 Phase 1, Phase 2 Aspirin Completed Univ. of Rochester 
A Pharmacokinetic (PK) and Pharmacodynamic (PD) Dose-ranging Phase II Study of Ticagrelor Followed by a 4 Weeks Extension Phase in Pediatric Patients With Sickle Cell Disease NCT02214121 Phase 2 Ticagrelor Recruiting AstraZeneca 
A Study to Evaluate the Effect of Ticagrelor in Reducing the Number of Days With Pain in Patients With Sickle Cell Disease (Hestia2) NCT02482298 Phase 2 Ticagrelor Recruiting AstraZeneca 
Study titleClinical trials #/PhaseInterventionStatusPrimary sponsor
Abciximab (ReoPro) as a Therapeutic Intervention for Sickle Cell Vaso-Occlusive Pain Crisis NCT01932554 Phase 2 Abciximab Withdrawn St. Louis Univ. 
Dipyridamole/Magnesium To Improve Sickle Cell Hydration NCT00276146 Phase 2 Dipyridamole, Magnesium Withdrawn Children's Hospital Medical Center, Cincinnati 
A Phase I/II Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety of Eptifibatide as Treatment of Acute Pain Episodes in Sickle Cell Disease NCT00834899 Phase 1, 2 Eptifibatide Terminated Univ. of North Carolina-Chapel Hill 
An Assessment of Prasugrel on Healthy Adults and Sickle Cell Adults NCT01178099 Phase 1 Prasugrel Completed Ely Lilly 
A Study of Prasugrel in Pediatric Participants With Sickle Cell Disease NCT01476696 Phase 2 Prasugrel Completed Ely Lilly 
Prasugrel Versus Placebo in Adult Sickle Cell Disease NCT01167023 Phase 2 Prasugrel Completed Ely Lilly 
A Phase 3, Double-Blind, Randomized, Efficacy and Safety Comparison of Prasugrel and Placebo in Pediatric Patients With Sickle Cell Disease. NCT01794000 Phase 3 Prasugrel Active, not recruiting Eli Lilly 
Aspirin Prophylaxis in Sickle Cell Disease NCT00178464 Phase 1, Phase 2 Aspirin Completed Univ. of Rochester 
A Pharmacokinetic (PK) and Pharmacodynamic (PD) Dose-ranging Phase II Study of Ticagrelor Followed by a 4 Weeks Extension Phase in Pediatric Patients With Sickle Cell Disease NCT02214121 Phase 2 Ticagrelor Recruiting AstraZeneca 
A Study to Evaluate the Effect of Ticagrelor in Reducing the Number of Days With Pain in Patients With Sickle Cell Disease (Hestia2) NCT02482298 Phase 2 Ticagrelor Recruiting AstraZeneca 
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