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Starting soon Phase 2

Vortosiran in Atrial Fibrillation

NCT07870889 · tracked via the Priya Life Science Denmark tracker
Phase
Phase 2
Started
2026-10-01
Last updated
2026-10-13

Condition(s) studied

Non-valvular Atrial Fibrillation (AF)

Investigational drug(s) / intervention(s)

Vortosiran →Vortosiran →Apixaban →

Vortosiran: Vortosiran, active drug

Vortosiran: Vortosiran, active drug

Apixaban: Comparator, active drug

Study summary

This is a randomised, actively controlled Phase IIb trial to evaluate the safety and pharmacodynamics (PD) of two blinded doses of subcutaneously administered vortosiran and open-label apixaban in patients with AF.

The trial consists of three groups including 50 participants each. The participants will be randomized to either the low dose group or the high dose group receiving vortosiran or to the group receiving apixaban. The treatment will be open-label for vortosiran vs apixaban. The vortosiran dose will be blinded to patients and investigators.

Both the low- and the high-dose group will receive two doses of vortosiran, the first dose at Day X and the second at Day Y. After 24 weeks, at the end of the vortosiran treatment period, the participants will start an open-label part of the trial and will be switched to standard-of-care apixaban treatment until Week 64 (End of Trial; EOT). Participants in the open-label apixaban arm will receive apixaban as standard of care during the entire trial.

Eligibility

Sex
ALL
Min age
45 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Adult male and female participants, age \>/=45 years. 2. Documented diagnosis of non-valvular AF within 12 months of signing the informed consent (paroxysmal, persistent, or permanent) confirmed by ECG evidence (12-lead or other physician-confirmed electronic recording) and currently receiving continuous treatment with a DOAC for stroke prevention for at least the past 3 months. 3. Capable of giving signed informed consent. Written informed consent must be obtained before any trial procedure is initiated. 4. Postmenopausal women are eligible without additional contraceptive measures. Postmenopausal status is defined as: * Age \>/=55 years with \>/=12 months of spontaneous amenorrhea, or * Age \<55 years with \>/=12 months of spontaneous amenorrhea and follicle-stimulating hormone in the postmenopausal range, or surgical menopause (bilateral oophorectomy, with or without hysterectomy) documented in the medical history. 5. Women of childbearing potential must agree to use highly effective contraception for the duration of trial treatment and for the specified post-treatment period. Exclusion Criteria: 1. AF due to a reversible cause (e.g., cardiac surgery, pulmonary embolism, untreated hyperthyroidism, alcohol use), participants in sinus rhythm after successful ablation or planned for cardioversion or ablation during trial conduct. 2. Patients with an intracranial or intraocular bleed within the 3 months prior to screening or any history of spontaneous intracerebral haemorrhage at any time in the absence of antithrombotic treatment. 3. Any stroke within 14 days before randomisation or a transient ischemic attack within 3 days before randomisation. 4. Mechanical heart valve or valve disease that is expected to require mechanical valve replacement intervention (surgical or trans vascular) during the course of the trial. 5. Patients with a medical condition other than non-valvular AF for which chronic anticoagulation is indicated. 6. Known presence of an atrial myxoma or left ventricular thrombus. 7. History of or planned left atrial appendage closure or left atrial appendage removal. 8. Uncontrolled hypertension (systolic blood pressure \>/= 160 mmHg or diastolic blood pressure \>/=100 mmHg) at randomization. 9. Active bleeding, known bleeding disorder, or known anaemia that requires treatment or capillary Hgb \<100 g/L. 10. Any history of non-traumatic intracranial haemorrhage when not under treatment with an anticoagulant. 11. Known significant liver disease (e.g., acute hepatitis, chronic active hepatitis, cirrhosis) or hepatic insufficiency classified as Child-Pugh B or C, or alanine aminotransferase (ALT)/aspartate aminotransferase (AST) \>2.5 x the upper limit of normal, measured between screening and randomisation. 12. Estimated glomerular filtration rate (eGFR) \< 30 mL/min/1.73 m2 from the local lab, determined between screening and randomization. 13. Major surgery during the last 30 days or planned major surgery or intervention with potential for uncontrolled bleeding within the trial period (e.g., carotid endarterectomy, coronary artery bypass grafting). 14. Women who are pregnant, currently breastfeeding, or planning pregnancy during the trial or within the defined post-treatment period are not eligible. 15. Known allergy, intolerance, or hypersensitivity to any of the trial interventions. 16. Any contraindication for the use of an anticoagulant or listed in the local labelling for apixaban. 17. Anticipated need for chronic therapy with nonsteroidal anti-inflammatory drugs (NSAIDs): Patients with chronic NSAID use, defined as systemic NSAID therapy on \>/=3 days per week for at least 4 consecutive weeks prior to screening, are excluded. 18. Treated with a vitamin K antagonist within 3 months prior to screening. 19. Patients with a diagnosis of hepatitis B virus (HBV), hepatitis C virus (HCV) or human immunodeficiency virus (HIV) at screening. 20. Known current alcohol and / or illicit drug abuse that may interfere with the participant's safety and / or compliance at the discretion of the Investigator. 21. Male participants who are not willing to use condoms when sexually active with a woman of childbearing potential who is not using highly effective contraception. 22. Previous (within 30 days or 5 half-lives of the investigational drug, whichever is longer) or concomitant participation in another clinical trial with investigational medicinal product(s) or device(s). Registries and observational studies are allowed. 23. Any other condition or therapy that would make the participant unsuitable for the trial.

Primary outcome measure(s)

  • Primary objective — At week 16
    To evaluate the effect of vortosiran on change in coagulation Factor XI (FXI) activity
  • Primary endpoint — At week 16
    Change in FXI blood coagulation activity.

Trial sites (15)

FacilityCityRegionStatus
Frederiksberg Hospital Frederiksberg Denmark
Herlev-Gentofte Herlev Denmark
Sykehuset Østfold Kalnes Kardiologisk Grålum Norway
Akershus Universitetssykehus Ahus Kardiologisk Lørenskog Norway
EMC Silesia spółka z ograniczoną odpowiedzialnością Katowice Poland
Centrum Medyczne Vitamedicum Krakow Poland
Balsam Medica Sp z o.o. Raszyn Poland
Aidport Clinical Trial Hospital Skorzewo Poland
Centrum Medyczne LUX MED Warsaw Poland
Centrum Badań Klinicznych Wroclaw Poland
Centrum Medyczne Oporów Wroclaw Poland
Pracownia Badan Klinicznych Salus Wroclaw Poland
Danderyds Sjukhus - Hjärtmottagningen Danderyd Sweden
SUS Lund, Department of Cardiology Lund Sweden
Södersjukhuset, Department of Cardiology Stockholm Sweden

Other trials for the same condition

WATCHMAN FLX Pro European Registry Active, not recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07870889 on ClinicalTrials.gov ↗ ← All trials in Denmark