1200 Participants Needed

REGN7508 + REGN9933 for Atrial Fibrillation

(ROXI-ATLAS Trial)

Recruiting at 4 trial locations
CT
Overseen ByClinical Trials Administrator
Age: 18+
Sex: Any
Trial Phase: Phase 2
Sponsor: Regeneron Pharmaceuticals
Must be taking: Oral anticoagulants
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests two experimental drugs, REGN7508 and REGN9933, to determine their effectiveness in preventing blood clots in individuals with atrial fibrillation, a condition where the heart beats too fast and unevenly. Participants will receive either one of these new drugs or a commonly used medication, apixaban, for comparison. The study examines possible side effects, the drugs' potential to prevent strokes, and the body's reaction to them. Individuals with atrial fibrillation who require long-term blood-thinning medication might be eligible to join. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group, offering participants a chance to contribute to significant medical advancements.

Will I have to stop taking my current medications?

The trial information does not specify if you need to stop taking your current medications. However, if you are taking warfarin or another Vitamin K Antagonist, your Prothrombin Time/International Normalization Ratio (PT/INR) must be below 2.5 at the time of joining the study.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Research has shown that REGN7508 and REGN9933 are promising treatments for preventing blood clots in people with atrial fibrillation, an irregular and often fast heartbeat. REGN7508 effectively prevents clots while reducing the risk of bleeding, a common issue with blood thinners. Early results suggest it might even outperform some current treatments.

For REGN9933, studies indicate that it stops excessive blood clotting without interfering with other parts of the clotting process, potentially making it safer with fewer bleeding problems.

Both drugs are now in Phase 2 trials, meaning they have already undergone some human testing and are now being evaluated for efficacy and safety in a larger group. This phase often provides important safety information, and so far, these treatments appear well-tolerated.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about REGN7508 and REGN9933 for atrial fibrillation because they offer a novel approach compared to standard treatments like beta-blockers, calcium channel blockers, and anticoagulants. Unlike these traditional treatments, which mainly focus on controlling heart rate or rhythm and preventing blood clots, REGN7508 and REGN9933 may target specific pathways involved in the condition. This could potentially reduce side effects and improve outcomes for patients. Additionally, these new treatments might be more effective in maintaining normal heart rhythm over a longer period, offering hope for better long-term management of atrial fibrillation.

What evidence suggests that this trial's treatments could be effective for atrial fibrillation?

Research has shown that the drugs REGN7508 and REGN9933, studied in separate arms of this trial, may prevent blood clots without increasing bleeding risk. These drugs target coagulation factor XI (FXI), a component of blood that aids in clot formation. By blocking FXI, both REGN7508 and REGN9933 have reduced clotting events like venous thromboembolism (VTE), which can be dangerous. Specifically, REGN7508 demonstrated a 7% rate of VTE, while REGN9933 showed a 17% rate, meeting safety standards without causing major bleeding. These results suggest that these treatments could be effective for patients with atrial fibrillation, aiming to prevent strokes and related issues.13678

Who Is on the Research Team?

CT

Clinical Trial Management

Principal Investigator

Regeneron Pharmaceuticals

Are You a Good Fit for This Trial?

This trial is for adults with atrial fibrillation, a heart condition causing irregular and often rapid heartbeat. Participants must need ongoing anticoagulation treatment, have specific risk factors (CHA2DS2-VA score), and not be new to oral anticoagulants unless they meet certain criteria. Those on warfarin must have stable blood test results.

Inclusion Criteria

I have AF or flutter not caused by a temporary condition and need long-term blood thinners.
I have a risk score of 2 or higher for stroke and haven't taken blood thinners.
My blood clotting time is within safe limits while on blood thinners.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive REGN7508, REGN9933, or Apixaban to evaluate safety and effectiveness in preventing blood clots

12 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Apixaban
  • REGN7508
  • REGN9933
Trial Overview The study tests REGN7508 and REGN9933 against apixaban in preventing blood clots in atrial fibrillation patients. It aims to compare their effectiveness, measure drug levels in the blood, check for side effects, and see if the body develops antibodies against them.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Active Control
Group I: REGN9933Experimental Treatment1 Intervention
Group II: REGN7508Experimental Treatment1 Intervention
Group III: ApixabanActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Regeneron Pharmaceuticals

Lead Sponsor

Trials
690
Recruited
948,000+
Founded
1988
Headquarters
Tarrytown, USA
Known For
Precision medicine
Top Products
Dupixent, EYLEA, Libtayo, Praluent
Leonard Schleifer profile image

Leonard Schleifer

Regeneron Pharmaceuticals

Chief Executive Officer since 1988

MD and PhD in Medicine

George Yancopoulos profile image

George Yancopoulos

Regeneron Pharmaceuticals

Chief Medical Officer since 1997

MD from Harvard Medical School

Citations

Phase 2 Trials Demonstrating Antithrombotic Effect of Two ...REGN7508Cat is designed to maximize anticoagulant activity while minimizing bleeding risk, and REGN9933A2 is designed as an additional potential ...
Study Details | NCT07175428 | Safety in Adult Participants ...The aim of the study is to see how well REGN7508 and REGN9933 work in patients that get medicine for their atrial fibrillation. The bleeding effects of REGN7508 ...
Efficacy and safety of REGN9933 A2 and REGN7508 Cat ...Coagulation factor XI (FXI) inhibitors can reduce the incidence of thrombosis without increasing bleeding risk. FXI is activated by factor ...
Regeneron Advances Next-Generation Anticoagulant ...REGN7508 achieved a 7% incidence of venous thromboembolism (VTE), compared ... atrial fibrillation and post-surgical thrombosis prevention.
Phase 2 Trials Demonstrating Antithrombotic Effect of Two ...Proof-of-concept trials confirm robust anti-clotting effects for Regeneron's two mechanistically-distinct antibodies against factor XI, ...
Phase 2 Trials Demonstrating Antithrombotic Effect of Two ...REGN7508Cat is designed to maximize anticoagulant activity while minimizing bleeding risk, and REGN9933A2 is designed as an additional potential ...
Regeneron's Factor XI Antibodies Prevent ...A phase 2 trial has also been instigated to evaluate the safety of REGN7508 and REGN9933 versus apixaban in patients with atrial fibrillation.
Regeneron anticoagulant bests enoxaparin, matches EliquisREGN7508 proved the most successful of the two, with a single dose of the therapy demonstrating its superiority to daily doses of the approved factor Xa- ...
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