Lanadelumab in Long-term Prophylaxis of Acquired Angioedema
Part of paid clinical trials in Cincinnati, Ohio.
- Sponsor
- Bernstein Clinical Research Center
- Study ID
- NCT06818474
- Phase
- PHASE4
- Status
- Recruiting
Conditions
- Angioedema
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Lanadelumab 300 mg — BIOLOGICALno other intervention
Study Details
use of lanadelumab in patients with acquired angioedema
Key Dates
- Start date
- Jun 1, 2024
- Status verified
- Feb 2025
- Primary completion
- Sep 1, 2027
- Completion
- Dec 1, 2027
Study Design
- Enrollment
- 5 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Other: open-label administrationall subjects receive open-label lanadelumab
Primary Outcome Measure
Primary Objective [ Time Frame: 12 months ]
Central Contacts
- Karen Berendts513-354-1746
- Jonathan Bernstein, MD
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Bernstein Clinical Research Center, LLC | Cincinnati | Ohio | 45236 | Jonathan Bernstein, MD (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Cincinnati, OH
By research site
Related Studies
- Oral Deucrictibant for Prophylactic and Acute Treatment in Hereditary Angioedema PatientsPHASE1/PHASE2 · Recruiting · Institute for Asthma and Allergy · Wheaton, Maryland