drugset / Trial / NCT02615847

Clinical Trial to Study the Safety and Tolerability of Memantin Mepha® in Sickle Cell Disease Patients

NCT02615847

Phase 2 Completed 9 enrolled University of Zurich
NaSingle-groupOpen-labelTreatment

Summary

Symptomatic sickle cell disease is worldwide the most frequent cause for hereditary hemolytic anemia with recurrent pain crisis. Hemolysis, vaso- occlusive and pain crises are hallmarks of this disease and are causative for an important socio-economic burden worldwide, especially in Africa. Aside from allogenic stem cell transplantation, which is rarely available and very expensive, at present there is no curative treatment for patients with sickle cell disease (SCD). The current standard of care includes treatment with hydroxycarbamide and symptomatic care such as transfusions, antibiotic/analgesic treatment. This study has the aim to study the safety and tolerability of Memantin in patients with sickle cell disease.

Timeline

Start
2015-08
Primary completion
2017-03-31
Completion
2017-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Memantine Unknown 5 mg Oral
Subject Memantine Unknown 10 mg Oral
Subject Memantine Unknown 15 mg Oral
Subject Memantine Unknown 20 mg Oral

Indications