Alemtuzumab: clinical trials recruiting now
10
Recruiting trials
15
Conditions studied
5
US states with sites
2
Countries
FDA drug label
- FDA-approved
- Yes. Alemtuzumab appears in the FDA drug-label database. Marketed as Campath.
- Drug class
- CD52-directed Cytolytic Antibody (FDA established pharmacologic class)
- Mechanism of action
- CD52-directed Antibody Interactions (as stated on the FDA label)
- Boxed warning
- The FDA label for Alemtuzumab carries a boxed warning (the FDA's most serious warning). See the full label for details.
FDA-approved use
CAMPATH is indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL). CAMPATH is a CD52-directed cytolytic antibody indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL). ( 1 )
Phase breakdown
Phase 1 4
Phase 2 10
Conditions being studied
Recruiting trials involving Alemtuzumab
- Allo HSCT for High Risk Hemoglobinopathies
- Autologous Stem Cell Transplantation for Crohn's Disease
- Autologous Stem Cell Transplantation in Patients With Systemic Sclerosis
- Haploidentical Donor Hematopoietic Cell Transplant for Sickle Cell Disease
- Lung and Bone Marrow Transplantation for Lung and Bone Marrow Failure
- Nonmyeloablative Stem Cell Transplant in Children With Sickle Cell Disease and a Major ABO-Incompatible Matched Sibling Donor
- Partial Stem Cell Transplant for Sickle Cell Disease From Matched Donors
- Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT
- Sickle Cell Disease Transplant Using a Nonmyeloablative Approach for Patients With Anti-donor Red Cell Antibody
- T-Cell Depleted Alternative Donor Bone Marrow Transplant for Sickle Cell Disease (SCD) and Other Anemias
Common questions
Is Alemtuzumab FDA-approved?
Yes, marketed as Campath. Its FDA label carries a boxed warning.
How many recruiting trials involve Alemtuzumab?
10 recruiting trials across 15 conditions.
Is this list of trials complete?
No. For the full record, search ClinicalTrials.gov.