Factor XI LICA to Reduce Events Such as Heart Attack and Stroke in Patients Whose Kidneys Are no Longer Able to Work as They Should and Require Treatment to Filter Wastes From the Blood: Focus is on the Safety of BAY2976217 and the Way the Body Absorbs, Distributes and Removes the Study Drug

Completed · Phase 2 · Has a placebo group

Conditions studied: End Stage Renal Disease Requiring Hemodialysis

In brief

Patients whose kidneys are no longer able to work as they should and require treatment to filter wastes from the blood (hemodialysis) are at high risk for blood clots that form in blood vessels (thrombosis) blocking blood flow that causes heart attacks, strokes, and other life-threatening conditions. BAY2976217 is under clinical development for prevention of thrombosis. The goal of the study is to learn more about the safety of BAY2976217, how it is tolerated and the way the body absorbs, distributes and gets rid of the study dug given as multiple doses in participants with renal impairment who require hemodialysis.

Key facts

Study ID

NCT04534114

Run by

Bayer

People needed

307

Starts

2020-09-04

Expected to finish

2022-05-12

Last updated by the study team

2023-07-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant must be at least 18 years of age at the time of signing the informed consent form (ICF)
• Participants with ESRD on hemodialysis (HD) for ≥3 months at the time of signing of the ICF, receiving dialysis at least 9 hours a week and stable in the view of the investigator
• Male or female (contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies)
• Capable of giving signed ICF as described in the Protocol, which includes compliance with the requirements and restrictions listed in the ICF and in the protocol

You may not qualify if…

• Participants receiving antiplatelet therapy except daily acetylsalicylic acid (ASA) ≤ 150 mg/day
• Participants receiving anticoagulation in therapeutic doses, other than standard anticoagulation during the hemodialysis procedure
• Known inherited bleeding disorder e.g. von-Willebrand disease or Hemophilia A, B or C
• Recent (<6 months before screening) clinically significant bleeding, or at high risk of bleeding (in the judgement of the investigator)
• Recent (<3 months before screening) thromboembolic event, e.g. acute coronary syndrome, stroke, or Venous thromboembolism (except dialysis access thrombosis)
• Recent (<3 months before screening) major surgery or scheduled major surgery during participation in the study
• Scheduled living donor renal transplant during study participation
• Known Hepatitis B or C
• Known HIV with recent documented detectable viral load (<3 months before screening)
• Persistent heart failure as classified by the New York Heart Association classification of 3 or higher
• Life expectancy less than 6 months
• Sustained uncontrolled hypertension (persistent measurements of diastolic blood pressure ≥ 100 mmHg, and/or systolic blood pressure ≥ 180 mmHg)
• Hepatic disease associated with either: coagulopathy leading to a clinically relevant bleeding risk, or ALT > 3x ULN, or total bilirubin >2x ULN with direct bilirubin > 20% of the total
• Hb < 9.0 g/dL at screening
• Platelet count < 120,000 mm\^3 at screening
• Known hypersensitivity to the investigational drug or to inactive constituents of the study intervention
• Active malignancy requiring treatment during study participation (except non-melanoma skin cancer, or cervical carcinoma in situ)
• Participation in a study with an investigational medicinal product within 30 days or within 5 half-lives of the previous administered drug, whichever is longer, prior to the screening/observational period (Note: Participants from previous BAY2306001/ISIS 416858 and BAY2976217/ ION 957943 studies are eligible)
• Any other conditions, which, in the opinion of the investigator or Sponsor would make the subject unsuitable for inclusion
• Confirmed pregnancy

Where it is running

• Desert Cities Dialysis-Amethyst & Desert Cities Dialysis — Victorville, California, United States
• Davita East Ft. Lauderdale Dialysis Center — Fort Lauderdale, Florida, United States
• Fresenius Kidney Care St. Louis Regional Dialysis — Saint Ann, Missouri, United States
• Chromalloy Dialysis Center — St Louis, Missouri, United States
• Fresenius Medical Care - Fire Mesa Dialysis Unit — Las Vegas, Nevada, United States
• DaVita Northwest Medical Center Dialysis — San Antonio, Texas, United States
• San Antonio Kidney Disease Center Physicians Group, PLLC — San Antonio, Texas, United States
• Salem VA Medical Center — Salem, Virginia, United States
• OL Vrouwziekenhuis - Campus Aalst — Aalst, Belgium
• UZ Brussel — Bruxelles - Brussel, Belgium
• UZ Antwerpen — Edegem, Belgium
• Regionaal ZH Jan Yperman Campus Mariaziekenhuis — Ieper, Belgium
• First Dialysis Services Bulgaria Ead — Montana, Bulgaria
• MHAT Samokov — Samokov, Bulgaria
• MHAT "Knyaginya Klementina - Sofia"EAD — Sofia, Bulgaria
• MHAT National Cardiology Hospital EAD — Sofia, Bulgaria
• Etobicoke General Hospital — Etobicoke, Ontario, Canada
• St. Joseph's Healthcare - Hamilton — Hamilton, Ontario, Canada
• Lakeridge Health-Oshawa — Oshawa, Ontario, Canada
• Unity Health Toronto: St. Michael's Hospital — Toronto, Ontario, Canada
• Centre de services ambulatoires de dialyse de Gaspé — Montreal, Quebec, Canada
• CHU de Québec-Université Laval — Québec, Canada
• Nemocnice Frydek-Mistek — Frýdek-Místek, Czechia
• Klatovska nemocnice — Klatovy, Czechia
• Fresenius Kidney Care Clovis — Clovis, California, United States

Full record on ClinicalTrials.gov

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