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OpenTrials
Completed

NCT Number: NCT03427710

A First In Human Study to Assess CiVi007 in Subjects With an Elevated LDL-Cholesterol Level

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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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Leeds Clinic

Leeds, West Yorkshire, LS2 9LH, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Males or females, of any race, with fasting LDL C >2.6 mmol/L (100 mg/dL) and fasting serum triglycerides <4.52 mmol/L (400 mg/dL)
  • haematology and clinical chemistry without clinically significant abnormal values
  • Normal renal and hepatic function
  • Women must not be pregnant, lactating or of child bearing potential
  • Men must be willing to use appropriate contraception during the study
  • Able to comprehend and willing to sign an ICF and to abide by the study restrictions.

Key Exclusion Criteria:

  • Any uncontrolled or serious disease, or any medical or surgical condition
  • History or presence of coronary heart disease, peripheral artery disease, or cerebrovascular disease
  • Uncontrolled hypertension
  • Insulin dependent diabetes mellitus
  • Secondary dyslipidemia
  • History of renal or hepatic diseases, acquired immune deficiency syndrome, positive human immunodeficiency virus test and/or history of viral hepatitis B or C
  • History of cancer within 5 years
  • History of high alcohol consumption or positive alcohol breath test or urinary test for drugs of abuse
  • Participation in another clinical study within 3 months prior to screening or participation in another study
  • Use of treatment (e.g. antibody) towards PCSK9
  • History of multiple drug allergies or intolerance to subcutaneous injection.

Treatment and study plan

CiVi007

Drug

cholesterol lowering drug

Placebo

Other

matching placebo to CiVi007

Primary outcomes

  1. LDL Cholesterol

    Time frame: Maximum post dose within 8 weeks

    % LDL-C reduction

Secondary outcomes

  1. Peak Plasma Concentration (Cmax) of CiVi007

    Time frame: 8 weeks

    Pharmacokinetic Outcome Measure

  2. PCSK9 level

    Time frame: Maximum post dose within 8 weeks

    maximal % reduction in the level of circulating PCSK9

Sponsors and collaborators

Lead sponsor

Civi Biopharma, Inc.

Industry

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Feb 9, 2018
Registry last updated
Sep 22, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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