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Recruiting NCT07430397

A Single Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of CITY-FXI in Healthy Adults and Adults With FV Leiden or Prothrombin G20210A Mutation

Phase I Interventional Factor V Leiden Prothrombin G20210A

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: CITY-FXI, Placebo.
Who it may be relevant to
Registry conditions: Factor V Leiden, Prothrombin G20210A. Basic parameters: 18 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Phase 1, Randomised, Double-Blind, Placebo-Controlled Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CITY-FXI, a FXI Targeting siRNA, Administered Subcutaneously in Healthy Adults and Adults With Factor V Leiden or Prothrombin G20210A Mutation

Overview

This is a first-in-human (FIH), single-center, randomised, double-blind, placebo-controlled, single ascending dose (SAD) study evaluating the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of CITY-FXI in healthy adults and adults with Factor V Leiden (FVL) or prothrombin G20210A mutation.

Detailed description

The study will be conducted in two parts:

* Part A: Single Ascending Dose in Healthy Adults * Part B: Single Ascending Dose in Adults with Factor V Leiden (FVL) or Prothrombin G20210A Mutation

Interventions

  • Drug CITY-FXI
    siRNA (subcutaneous injection)
  • Drug Placebo
    Saline (subcutaneous injection)

Primary outcome measures

  • Incidence, severity, and relationship of treatment-emergent adverse events (TEAEs) [Time frame: Through study completion, up to Day 360]
Secondary outcome measures (6)
  • Maximum plasma concentration (Cmax) [Time frame: Day -1 to Day 3]
  • Area under plasma concentration time curve (AUC) of CITY-FXI [Time frame: Day -1 to Day 3]
  • Amount excreted in urine (Ae) of CITY-FXI [Time frame: Day -1 to Day 3]
  • Change from baseline in levels of plasma Factor XI (FXI) [Time frame: Up to Day 360]
  • Change from baseline of Factor XI (FXI) activity [Time frame: Up to Day 360]
  • Change from baseline in activated partial thromboplastin time (aPTT) [Time frame: Up to Day 360]

Eligibility criteria

Inclusion criteria

  • Males and women of non-childbearing potential (WONCBP) aged 18 to 45 years (Part A only)
  • Male and female participants aged 18 to 60 (Part B only)
  • Body Mass Index (BMI) between 18 and 25 kg/m2 (inclusive) and a minimum weight of 50 kg
  • Ability and willingness to comply fully with all study procedures and lifestyle considerations
  • Confirmed diagnosis of FVL or prothrombin G20210A mutation via genetic testing (Part B only)
  • Women of childbearing potential (WOCBP) must agree to use acceptable highly effective contraceptive methods (Part B only)

Exclusion criteria

  • Any clinically significant systemic disease or disorder, including but not limited to cardiovascular, hepatic, or oncological conditions
  • History or evidence of any bleeding disorders
  • History of clinically significant spontaneous bleeding
  • Prior treatment with an investigational agent
  • Confirmed diagnosis of homozygous mutations, or combined thrombophilic defects of (Part B only)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Sequential
Masking
Double blind
Primary purpose
Treatment

Study locations

United Kingdom · 1 center
  • Richmond Pharmacology — London

Identifiers

NCT: NCT07430397 · FXI-1101 · C24027

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗