EligibleTrials

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 )

FDA label via openFDA

Phase breakdown

Phase 1 4 Phase 2 10

Conditions being studied

ConditionTrials
Sickle Cell Disease · Alemtuzumab for Sickle Cell Disease7
Crohn's Disease2
Beta-thalassemia1
Beta-thalassemia Major1
COPD1
Congenital Bone Marrow Failure Syndromes1
Diamond-blackfan Anemia1
Diffuse Sclerosis Systemic1
Emphysema or COPD1
Graft Failure1
Hemoglobinopathies1
Hereditary Anemias1
Hypertension1
Idiopathic Pulmonary Fibrosis1
Inflammatory Conditions1

Recruiting trials involving Alemtuzumab

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.

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