Campath 1H
Campath 1H is a biological therapy with 13 clinical trials. Historical success rate of 30.8%.
Success Metrics
Based on 4 completed trials
Phase Distribution
Phase Distribution
7
Early Stage
4
Mid Stage
0
Late Stage
Highest Phase Reached
Phase 2Trial Status & Enrollment
30.8%
4 of 13 finished
69.2%
9 ended early
0
trials recruiting
13
all time
Detailed Status
Development Timeline
Analytics
Development Status
Trials by Phase
Trials by Status
Recent Activity
Donor Stem Cell Transplantation for Congenital Immunodeficiencies
Bone Marrow Transplantation, Hemoglobinopathies, SCALLOP
Allogeneic Stem Cell Transplantation, Severe Homzygous 0/+Thalassemia or Sever Variants of Beta 0/+ Thalassemia, THALLO
Stem Cell Transplantation for Patients With Graft Failure Following an Allogeneic Transplant, Using Identical or Near Identical Donors and Less Toxic Conditioning With CAMPATH 1H
Bone Marrow Transplant From Related Donor for Patients With High Risk Hemoglobinopathies
Clinical Trials (13)
Donor Stem Cell Transplantation for Congenital Immunodeficiencies
Bone Marrow Transplantation, Hemoglobinopathies, SCALLOP
Allogeneic Stem Cell Transplantation, Severe Homzygous 0/+Thalassemia or Sever Variants of Beta 0/+ Thalassemia, THALLO
Stem Cell Transplantation for Patients With Graft Failure Following an Allogeneic Transplant, Using Identical or Near Identical Donors and Less Toxic Conditioning With CAMPATH 1H
Bone Marrow Transplant From Related Donor for Patients With High Risk Hemoglobinopathies
Stem Cell Transplant for Patients With Blood Malignancy Using Donors and Less Toxic Chemotherapy With CAMPATH 1H
Rheumatoid Arthritis:Tolerance Induction by Mixed Chimerism
Stem Cell Transplant for Immunologic or Histiocytic Disorders
Stem Cell Transplant (SCT) for Dyskeratosis Congenita or SAA
Stem Cell Transplant for Hematologic Diseases
Use of Rft5-Dga to Deplete Alloreactive Cells for Pts With Fanconi Anemia After Haploidentical SCT
Allogeneic SCT Of Pts With SCID And Other Primary Immunodeficiency Disorders
Total-Body Irradiation, Fludarabine, and Alemtuzumab Followed By Stem Cell Transplant in Treating Patients With Myeloproliferative Disorder, MS, AML, or CML
All 13 trials loaded
Drug Details
- Intervention Type
- BIOLOGICAL
- Total Trials
- 13