A Phase 2/ 3 Trial to Evaluate the Efficacy and Safety of BAY86-6150

Completed · Phase 2/Phase 3

Conditions studied: Hemophilia A, Hemophilia B

In brief

Haemophilia is a disorder, usually genetic, affecting mostly male individuals, in which one of the proteins needed to form blood clots (FVIII) is missing or not present in sufficient levels. In a person with haemophilia, the clotting process is much slower and the person experiences bleeding episodes that can result in serious problems and potential disability. The current haemophilia standard of care is to maintain FVIII activity level above 1%. Sometimes, patients can develop antibodies (so called "inhibitors") against FVIII and it is no longer effective at controlling bleeds. Bleeds in these patients are currently treated using other proteins involved in the clotting process. The purpose of this study is to investigate how effectively BAY86-6150 may stop acute bleeds in "inhibitor" patients. This study consists of two parts, A and B. The purpose of part A is to find the most effective yet tolerable out of four doses of BAY86-6150 with regard to efficacy and safety (dose-finding part). Part A is expected to last 9 - 29 months. The purpose of part B is to confirm efficacy and safety of the dose found in part A in all participating patients (confirmatory part). Part B is expected to last 12-32 months. Approximately 60 male subjects 12 to 62 years-of-age with moderate or severe haemophilia A or B, with inhibitors to FVIII or FIX, who have had 4 or more bleeding episodes in the last 6 months, will participate in this study. Patient's bleeds will be treated with BAY86-6150 and with a rescue medication if no response is made to BAY86-6150. Patients will attend the treatment centre at regular intervals and be required to keep an electronic diary.

Key facts

Study ID

NCT01625390

Run by

Bayer

People needed

10

Starts

2012-06-01

Expected to finish

2014-03-01

Last updated by the study team

2015-07-01

Who can join

Age: 12 and older, up to 62. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Male subjects
• 12 to 62 years-of-age
• History of moderate or severe congenital hemophilia A or B with inhibitors to FVIII or FIX
• 4 or more bleeding episodes in the last 6 months before enrollment.

You may not qualify if…

• Clinically relevant coagulation disorder other than congenital hemophilia A or B with inhibitors
• History of coronary and/or peripheral atherosclerotic disease
• Disseminated intravascular coagulopathy, or stage 2 hypertension
• Angina pectoris
• Myocardial infarction
• Transient ischemic attack
• Stroke
• Congestive heart failure
• Thromboembolic event

Where it is running

• Study site — Chattanooga, Tennessee, United States
• Study site — Melbourne, Victoria, Australia
• Study site — Rio de Janeiro, Rio de Janeiro, Brazil
• Study site — São Paulo, São Paulo, Brazil
• Study site — São Paulo, São Paulo, Brazil
• Study site — Sofia, Bulgaria
• Study site — Santiago, Chile
• Study site — Guangzhou, Guangdong, China
• Study site — Beijing, China
• Study site — Tianjin, China
• Study site — Barranquilla, Atlántico, Colombia
• Study site — Bogotá, Colombia
• Study site — Aarhus N, Denmark
• Study site — Lyon, France
• Study site — Tours, France
• Study site — Villingen-Schwenningen, Baden-Wurttemberg, Germany
• Study site — Mainz, Rhineland-Palatinate, Germany
• Study site — Budapest, Hungary
• Study site — Debrecen, Hungary
• Study site — Hyderabad, Andhra Pradesh, India
• Study site — Ludhiana, Punjab, India
• Study site — Bangalore, India
• Study site — Pune, India
• Study site — Tel Litwinsky, Israel
• Study site — Sacramento, California, United States

Full record on ClinicalTrials.gov

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