Anti-Factor XI Monoclonal Antibody for Kidney Failure
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called MK-2060, a monoclonal antibody designed to assist people with end-stage renal disease (ESRD) undergoing hemodialysis. The goal is to determine if two different doses of MK-2060 can safely and effectively delay complications with the arteriovenous graft (AVG), a special connection used for dialysis. Participants will receive either a high dose, a low dose, or a placebo for comparison. Those who have been on regular hemodialysis with a well-functioning AVG for at least four weeks may be suitable for this trial. As a Phase 2 trial, the research focuses on measuring the treatment's effectiveness in an initial, smaller group of people.
Will I have to stop taking my current medications?
The trial requires that you do not take anticoagulants or antiplatelet medications, except for heparin during dialysis and aspirin. If you are on other blood thinners, you may need to stop them.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that MK-2060, a monoclonal antibody, is under evaluation for safety and effectiveness in people with end-stage kidney disease. Earlier studies found that MK-2060 does not significantly increase bleeding risk in these patients, suggesting it might be well-tolerated. Additionally, no reports of serious side effects have been directly linked to MK-2060 in the available research. The current study is in the middle stages of clinical trials, indicating that early safety results are positive, but further research is needed to confirm these findings.12345
Why are researchers excited about this trial's treatments?
Researchers are excited about MK-2060 for kidney failure because it targets Factor XI, a key component in blood clot formation, using a monoclonal antibody approach. Unlike standard treatments that might focus on managing symptoms or other pathways, MK-2060 directly interrupts the coagulation cascade, potentially reducing the risk of blood clots without the same bleeding risks associated with traditional anticoagulants. Additionally, the treatment is administered via intravenous infusion, which might offer a controlled delivery method compared to oral medications, ensuring precise dosing and potentially improving outcomes.
What evidence suggests that this trial's treatments could be effective for kidney failure?
Research has shown that MK-2060, a type of antibody, has not significantly reduced blood clots in patients with severe kidney disease on dialysis. In this trial, participants will receive either a high dose or low dose of MK-2060, or a placebo. Studies comparing MK-2060 to a placebo found it ineffective in preventing clots in the blood vessels used for dialysis. While researchers are studying MK-2060 for its potential to prevent blood clots, current evidence does not support its effectiveness for this purpose. Ongoing research aims to better understand its role and possible benefits.12345
Who Is on the Research Team?
Medical Director
Principal Investigator
Merck Sharp & Dohme LLC
Are You a Good Fit for This Trial?
This trial is for adults with end-stage renal disease (ESRD) who are on hemodialysis through an arteriovenous graft. Participants must not be pregnant, agree to contraception if of childbearing potential, and have had stable dialysis sessions. Exclusions include recent cancer or strokes, recurrent bleeding episodes, substance abuse history, and those on certain blood thinners.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive either MK-2060 or placebo via IV infusion with a loading dose every other day during week 1, then once a week after week 1
Follow-up
Participants are monitored for safety and effectiveness after treatment, including monitoring for adverse events and bleeding events
What Are the Treatments Tested in This Trial?
Interventions
- MK-2060
Find a Clinic Near You
Who Is Running the Clinical Trial?
Merck Sharp & Dohme LLC
Lead Sponsor
Chirfi Guindo
Merck Sharp & Dohme LLC
Chief Marketing Officer since 2022
Degree in Engineering from Ecole Centrale de Paris, MBA from New York University Stern School of Business
Robert M. Davis
Merck Sharp & Dohme LLC
Chief Executive Officer since 2021
JD from Northwestern University Pritzker School of Law, MBA from Northwestern University Kellogg Graduate School of Management, Bachelor's in Finance from Miami University
Merck Sharp & Dohme Corp.
Lead Sponsor
Chirfi Guindo
Merck Sharp & Dohme Corp.
Chief Medical Officer
Engineering degree from Ecole Centrale de Paris, MBA from New York University Stern School of Business
Robert M. Davis
Merck Sharp & Dohme Corp.
Chief Executive Officer since 2021
J.D. from Northwestern University Pritzker School of Law, MBA from Northwestern University Kellogg Graduate School of Management, Bachelor's in Finance from Miami University