REGN7508
DrugAdministered per the protocol
Other names: cenvacibart
NCT Number: NCT07430956
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)
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 3
SEC Clinical Research, Dothan, Alabama, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Note: Other protocol-defined Inclusion/ Exclusion criteria apply
Administered per the protocol
Other names: cenvacibart
Administered per the protocol
Other names: amrecibart
Administered per the protocol
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 39 months
Time frame: Up to 39 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to approximately 9 weeks
Time frame: Up to approximately 9 weeks
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Time frame: Up to 36 months
Contact information is provided by the study sponsor or research team.
Regeneron Pharmaceuticals
Industry
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
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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