Glanzmann thrombasthenia 1
Glanzmann thrombasthenia 1
Explore linked clinical trials. Standard reference: MONDO:00313326 results · Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| A Phase 1/2 Study to Investigate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of HMB-001 in Glanzmann Thrombasthenia | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, blood coagulation disease, blood platelet disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder | Active, not recruiting | Phase 1 / Phase 2 | 2026-09-25 | NCT06211634 | |
| Videomicroscopy for the Prediction of Bleeding in Constitutional Haemorrhagic Diseases | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, blood coagulation disease, blood platelet disease, coagulation protein disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder, von Willebrand disease (hereditary or acquired) | Recruiting | Not applicable | 2026-05-20 | NCT04119908 | |
| ATHNdataset Registry | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Embolism and Thrombosis, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, X-linked disease, anemia, arthropathy, blood coagulation disease, blood platelet disease, cardiovascular disorder, coagulation protein disease, familial hemolytic anemia, hemarthrosis, hematologic disorder, hemolytic anemia, hemophilia A, hemophilia B, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder, inherited hemoglobinopathy, musculoskeletal system disorder, sickle cell disease, thrombotic disease, vascular disorder, vascular hemostatic disease, von Willebrand disease (hereditary or acquired) | Recruiting | Not stated | 2026-04-21 | NCT06820515 | |
| Eptacog Beta in Glanzmann's (HeT_LFB-Strength-Study_FID531) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, Hemorrhage, Pathologic Processes, Pathological Conditions, Signs and Symptoms, blood coagulation disease, blood platelet disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder | Recruiting | Phase 2 | 2025-12-01 | NCT07136857 | |
| The Genetics and Functional Basis of Inherited Platelet, White Blood Cell, Red Blood Cell, and Blood Clotting Disorders. | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Embolism and Thrombosis, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, blood coagulation disease, blood platelet disease, cardiovascular disorder, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder, thrombotic disease, vascular disorder | Recruiting | Not stated | 2025-10-20 | NCT00230165 | |
| Multinational Glanzmann Study | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Glanzmann thrombasthenia 1, Hemic and Lymphatic Diseases, blood coagulation disease, blood platelet disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder | Not yet recruiting | Not stated | 2024-02-28 | NCT06204042 |