Leeds Clinic
Leeds, West Yorkshire, LS2 9LH, United Kingdom
NCT Number: NCT03427710
The primary objective of the study is to assess pharmacokinetics, dynamics, safety and tolerability of CiVi007 following single and multiple subcutaneous doses in subjects, including those on statin therapy
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Notify Me18 year–50 year
All sexes
Interventional
Phase 1
Leeds, West Yorkshire, LS2 9LH, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
cholesterol lowering drug
matching placebo to CiVi007
Time frame: Maximum post dose within 8 weeks
% LDL-C reduction
Time frame: 8 weeks
Pharmacokinetic Outcome Measure
Time frame: Maximum post dose within 8 weeks
maximal % reduction in the level of circulating PCSK9
Civi Biopharma, Inc.
Industry
A Placebo-controlled, Single Blind, Randomised, Phase I, First In Human Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Subcutaneously Administered CiVi007 in Subjects With an Elevated LDL C Level
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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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