Regeneron Research Site
Antwerp, B-2060, Belgium
NCT Number: NCT04601844
The primary objective of the study is to evaluate the safety and tolerability of ascending doses of subcutaneous (SC) pozelimab and SC cemdisiran when administered on the same day or sequentially 28 days apart.
The secondary objectives of the study are:
* To assess the concentration-time profiles of total pozelimab, total complement component 5 (C5), cemdisiran, and cemdisiran metabolite(s) following single ascending doses of SC pozelimab and SC cemdisiran when administered on the same day or sequentially 28 days apart * To assess the pharmacodynamic (PD) profile of ascending doses of SC pozelimab and SC cemdisiran, as well as when administered on the same day or sequentially 28 days apart * To assess the immunogenicity of pozelimab and cemdisiran
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Notify Me18 year–55 year
All sexes
Interventional
Phase 1
Antwerp, B-2060, Belgium
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
NOTE: Other protocol-defined Inclusion/ Exclusion criteria apply
Single dose administered subcutaneously
Other names: REGN3918
Single dose administered SC
Other names: ALN-CC5
Time frame: Up to 20 weeks
Time frame: Up to 20 weeks
Time frame: Up to 20 weeks
Time frame: Up to 20 weeks
Time frame: Up to 20 weeks
Time frame: Up to 20 weeks
Time frame: Up to 20 weeks
Regeneron Pharmaceuticals
Industry
An Open-Label, Ascending Dose Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Doses of Subcutaneously Administered Human Monoclonal Antibody Pozelimab in Combination With Single Doses of Subcutaneously Administered siRNA Cemdisiran in Healthy Volunteers
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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