Wiskott-Aldrich Syndrome
31
0
4
17
Key Insights
Highlights
Success Rate
77% trial completion
Clinical Risk Assessment
Based on trial outcomes
Moderate Risk
Score: 49/100
16.1%
5 terminated out of 31 trials
77.3%
-9.2% vs benchmark
13%
4 trials in Phase 3/4
47%
8 of 17 completed with results
Key Signals
Data Visualizations
Phase Distribution
Trial Status
Trial Success Rate
Benchmark: 86.5%
Based on 17 completed trials
Clinical Trials (31)
Immune Disorder HSCT Protocol
Allogeneic Hematopoietic Stem Cell Transplant for Patients With Primary Immune Deficiencies
Sequential Cadaveric Lung and Bone Marrow Transplant for Immune Deficiency Diseases
A Clinical Study to Evaluate the Use of a Cryopreserved Formulation of OTL-103 in Subjects With Wiskott-Aldrich Syndrome
Pilot and Feasibility Study of Hematopoietic Stem Cell Gene Transfer for the Wiskott-Aldrich Syndrome
Baby Detect : Genomic Newborn Screening
Fludarabine Phosphate, Cyclophosphamide, Total Body Irradiation, and Donor Stem Cell Transplant in Treating Patients With Blood Cancer
Conditioning Regimen for Allogeneic Hematopoietic Stem-Cell Transplantation
Participation in a Research Registry for Immune Disorders
Long Term Safety Follow up of Haematopoietic Stem Cell Gene Therapy for the Wiskott Aldrich Syndrome
Gene Therapy for Wiskott-Aldrich Syndrome (WAS)
Romiplostim Treatment for Thrombocytopenia in Patients With Wiskott-Aldrich Syndrome.
Patients Treated for Wiskott-Aldrich Syndrome (WAS) Since 1990
Efficacy and Safety of Romiplostim Versus Eltrombopag in the Treatment of Thrombocytopenia in Patients With Wiskott-Aldrich Syndrome
Bone Marrow Transplant With Abatacept for Non-Malignant Diseases
Fludarabine Phosphate, Melphalan, and Low-Dose Total-Body Irradiation Followed by Donor Peripheral Blood Stem Cell Transplant in Treating Patients With Hematologic Malignancies
Thrombocytopenia and Bleeding in Wiskott-Aldrich Syndrome (WAS) Patients
Targeted Literature Review and Subject Interviews in Wiskott-Aldrich Syndrome (WAS)
A Trial of Plerixafor/G-CSF as Additional Agents for Conditioning Before TCR Alpha/Beta Depleted HSCT in WAS Patients
Gene Therapy for WAS