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NCT Number: NCT07430956

Stroke and Systemic Embolism Prevention in Adult Participants With Atrial Fibrillation for Whom Oral Anticoagulation is Unsuitable

This study is researching 2 different experimental drugs called REGN7508 and REGN9933 (called "study drugs"). The study is focused on people who have atrial fibrillation, which means that the heart beats too fast and unevenly. When this happens, blood cannot move smoothly through the heart; it can slow down or pool in one spot, which can lead to the formation of blood clots.

REGN7508 and REGN9933 are designed to help stop blood clots forming in patients with atrial fibrillation. The aim of the study is to see how effective and safe REGN7508 and REGN9933, individually, are in preventing ischemic stroke or systemic embolism in people with atrial fibrillation who cannot or may choose to not take blood thinners.

The study is looking at several other research questions, including:

* What side effects may happen from taking REGN7508 or REGN9933 * How well does REGN7508 or REGN9933 lower the risk of having an ischemic stroke and/or systemic embolism compared to the placebo * How well does REGN7508 or REGN9933 lower the risk of having a major health problem affecting heart and blood circulation compared to placebo * How well does REGN7508 or REGN9933 lower the risk of death compared to placebo * How much REGN7508 or REGN9933 is in the blood at different times * Whether the body makes antibodies against REGN7508 or REGN9933 (which could make the study drugs less effective or could lead to side effects)

Recruiting

Interested in participating?

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Key information

Who can participate

Healthy volunteers accepted: No

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

Key Inclusion Criteria:

  • Has AF or flutter (paroxysmal or persistent), not considered to be secondary to a reversible cause
  • At moderate to high risk for stroke defined as:
  • CHA2DS2-VA [C: Congestive heart failure; H: Hypertension; A2: Age ≥75 years (double points); D: Diabetes mellitus; S2: Stroke or TIA or Systemic embolism (double points); V: Vascular disease; A: Age 65-74 years] score ≥4 OR
  • CHA2DS2-VA score of 3 AND at least 1 enrichment criteria as described in the protocol
  • Shared decision making between the participant and provider determining that the bleeding risk of Oral Anticoagulant (OAC) therapy outweighs the benefits, making the participant unsuitable for OAC therapy as described in the protocol

Key Exclusion Criteria:

  • Has a mechanical heart valve prosthesis (Note: transcatheter aortic valve replacement is not an exclusion)
  • Had an ischemic stroke within 2 days prior to randomization
  • Has persistent, uncontrolled hypertension (per investigator's discretion)
  • Has a history of Central Nervous System (CNS) bleeding within 30 days prior to randomization
  • Has a life expectancy less than 12 months
  • Has participated in a prior Factor XI (FXI) inhibitor study

Note: Other protocol-defined Inclusion/ Exclusion criteria apply

Treatment and study plan

REGN7508

Drug

Administered per the protocol

Other names: cenvacibart

REGN9933

Drug

Administered per the protocol

Other names: amrecibart

Placebo

Drug

Administered per the protocol

Primary outcomes

  1. Time to first occurrence of ischemic stroke or systemic embolism

    Time frame: Up to 36 months

  2. Time to first occurrence of International Society on Thrombosis and Haemostasis (ISTH) major bleeding

    Time frame: Up to 36 months

Secondary outcomes

  1. Time to first occurrence of Major Adverse Cardiovascular Event (MACE)

    Time frame: Up to 36 months

  2. Time to first occurrence of MACE, pulmonary embolism, or Venous Thromboembolism (VTE)

    Time frame: Up to 36 months

  3. Time to first occurrence of ischemic stroke

    Time frame: Up to 36 months

  4. Time to Cardiovascular (CV) death

    Time frame: Up to 36 months

  5. Time to all-cause death

    Time frame: Up to 36 months

  6. Occurrence of Treatment-Emergent Adverse Events (TEAEs)

    Time frame: Up to 39 months

  7. Severity of TEAEs

    Time frame: Up to 39 months

  8. Concentrations of REGN7508 over time

    Time frame: Up to 36 months

  9. Concentrations of REGN9933 over time

    Time frame: Up to 36 months

  10. Change from baseline in activated Partial Thromboplastin Time (aPTT) over time

    Time frame: Up to approximately 9 weeks

  11. Change from baseline in Prothrombin time (PT)/International Normalized Ratio (INR) over time

    Time frame: Up to approximately 9 weeks

  12. Occurrence of Anti-Drug Antibody (ADA) to REGN7508 over time

    Time frame: Up to 36 months

  13. Magnitude of ADA to REGN7508 over time

    Time frame: Up to 36 months

  14. Occurrence of ADA to REGN9933 over time

    Time frame: Up to 36 months

  15. Magnitude of ADA to REGN9933 over time

    Time frame: Up to 36 months

Study contacts

Contact information is provided by the study sponsor or research team.

Clinical Trials Administrator

CONTACT

[email protected]

844-734-6643

Sponsors and collaborators

Lead sponsor

Regeneron Pharmaceuticals

Industry

Registry information

Official study title

A Master Protocol for a Phase 3, Randomized, Multicenter, Double-blind Study to Assess Stroke and Systemic Embolism Prevention With REGN7508 and REGN9933, Monoclonal Antibodies Against Factor XI, Versus Placebo in Participants With Atrial Fibrillation for Whom Oral Anticoagulation is Unsuitable (ROXI-INCLINE)

Acronym: ROXI-INCLINE

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Feb 24, 2026
Registry last updated
Jun 23, 2026

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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