Depemokimab: clinical trials recruiting now
FDA drug label
- FDA-approved
- Yes. Depemokimab appears in the FDA drug-label database. Marketed as Exdensur.
FDA-approved use
EXDENSUR is indicated for the add‑on maintenance treatment of severe asthma characterized by an eosinophilic phenotype in adult and pediatric patients aged 12 years and older. Limitations of Use EXDENSUR is not indicated for the relief of acute bronchospasm or status asthmaticus [see Warnings and Precautions ( 5.2 )] . EXDENSUR is an interleukin‑5 (IL‑5) antagonist, a monoclonal antibody (humanized immunoglobulin G1 [IgG1] kappa) indicated for add‑on maintenance treatment of severe asthma characterized by an eosinophilic phenotype in adult and pediatric patients aged 12 years and older. ( 1 ) Limitations of Use : Not for relief of acute bronchospasm or status asthmaticus. ( 1 )
Phase breakdown
Conditions being studied
| Condition | Trials |
|---|---|
| Asthma · Depemokimab for Asthma | 3 |
| COPD · Depemokimab for COPD | 3 |
| Pulmonary Disease, Chronic Obstructive · Depemokimab for Pulmonary Disease, Chronic Obstructive | 3 |
Recruiting trials involving Depemokimab
- A Study of Depemokimab in Participants of 6 to 11 Years of Age
- A Study of Efficacy and Safety of Depemokimab Compared With Placebo in Adults and Adolescents With at Risk Type 2 Asthma
- Depemokimab Asthma Imaging and Bronchoscopy Sub-Study
- Depemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA -1)
- Depemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA-2)
- eValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 Inflammation
Common questions
Is Depemokimab FDA-approved?
Yes, marketed as Exdensur.
How many recruiting trials involve Depemokimab?
6 recruiting trials across 3 conditions.
Is this list of trials complete?
No. For the full record, search ClinicalTrials.gov.