Safety of Anumigilimab (CSL324) in Adults With Sickle Cell Disease (SCD)

Recruiting Phase 2 Interventional Study
Sickle Cell Disease
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
63 (estimated)
Sponsor
CSL Behring · Industry
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About This Trial
This is a phase 2a, global, multicenter, randomized, double-blind, placebo-controlled study investigating the safety of anumigilimab administered subcutaneously (SC) at the maximum tolerated dose (MTD) in adult participants with SCD. The primary aim of the study is to assess the safety of anumigilimab in participants with SCD. Participants will be treated for 64 weeks: for 12 weeks in the dose es…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adults aged greater than or equal to (\>=) 18 years on the day of signing the informed consent form. * Confirmed diagnosis of SCD of any genotype. * Experienced 1 to 12 VOCs requiring a visit to a medical facility and treatment with parenteral opioids or a parenteral nonsteroi…
Contacts

Trial Registration Coordinator

+1 610-878-4697

clinicaltrials@cslbehring.com

CONTACT