Research Study to Look at How Well the Drug Concizumab Works in Your Body if You Have Haemophilia With Inhibitors

Running, not enrolling · Phase 3

Conditions studied: Haemophilia A With Inhibitors, Haemophilia B With Inhibitors

In brief

This study will test how well a new medicine called concizumab works in the body of people with haemophilia A or B with inhibitors. The purpose is to show that concizumab can prevent bleeds in the body and is safe to use. Participants who usually only take medicine to treat bleeds (on-demand) will be placed in one of two groups. In one group, participants will get study medicine from the start of the study. In the other group, participants will continue with their normal medicine and get study medicine after 6 months. Which treatment the participant gets is decided by chance. Participants who usually take medicine to prevent bleeds (prophylaxis treatment) or who are already being treated with concizumab (study medicine) will receive the study medicine from the start of the study. Participants will get 1 injection with the study medicine every day under the skin. This participants will have to do themselves and can be done at home. The study doctor will hand out the medicine in the form of a pen-injector. The pen-injector will contain the study medicine. The study will last for about seven years. The length of time the participants will be in the study depends on when they agreed to take part or when the medicine is available for purchase in their country (31 December 2026 at the latest). The time between visits will be approximately 4 weeks for the first 6 to 12 months, depending on the group participants are in and approximately 8 weeks for the rest of the study. Participants will be asked to record information into an electronic diary during the study and may also be asked to wear an activity tracker.

Key facts

Study ID

NCT04083781

Run by

Novo Nordisk A/S

People needed

134

Starts

2019-10-21

Expected to finish

2027-02-21

Last updated by the study team

2026-06-12

Who can join

Age: any. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Informed consent obtained before any trial-related activities. Trial-related activities are any procedures that are carried out as part of the trial, including activities to determine suitability for the trial.
• Male aged 12 years or older at the time of signing informed consent.
• Congenital Haemophilia A or B of any severity with documented history of inhibitor (equal to or above 0.6 Bethesda Units (BU).
• Patient has been prescribed, or in need of, treatment with bypassing agents in the last 24 weeks prior to screening (for patients not previously enrolled in NN7415-4310 (explorer 4)).

You may not qualify if…

• Known or suspected hypersensitivity to any constituent of the trial product or related products.
• Known inherited or acquired coagulation disorder other than congenital haemophilia.
• Ongoing or planned Immune Tolerance Induction treatment.
• History of thromboembolic disease (includes arterial and venous thrombosis including myocardial infarction, pulmonary embolism, cerebral infarction/thrombosis, deep vein thrombosis, other clinically significant thromboembolic events and peripheral artery occlusion). Current clinical signs of, or treatment for thromboembolic disease. Patients who in the judgement of the investigator are considered at high risk of thromboembolic events (thromboembolic risk factors could include, but are not limited to, hypercholesterolemia, diabetes mellitus, hypertension, obesity, smoking, family history of thromboembolic events, arteriosclerosis, other conditions associated with increased risk of thromboembolic events.)

Where it is running

• Children's Healthcare Atlanta — Atlanta, Georgia, United States
• Indiana Hemophilia-Thromb Ctr — Indianapolis, Indiana, United States
• Washington University School of Medicine_St. Louis — St Louis, Missouri, United States
• St. Jude Affiliate Clinic at Novant Health Hemby Children's — Charlotte, North Carolina, United States
• TriStar Medical Group Children's Specialist — Nashville, Tennessee, United States
• University of Texas San Antonio — San Antonio, Texas, United States
• Haematology and Blood Bank Department — Algiers, Algeria
• CHU Constantine BEN BADIS/ Hematology department — Constantine, Algeria
• The Alfred — Melbourne, Victoria, Australia
• The Royal Children's Hospital — Parkville, Victoria, Australia
• Fiona Stanley Hospital - Haemophilia and Haemostasis Centre — Murdoch, Western Australia, Australia
• Klin. Abt. f. Hämatologie und Hämostaseologie, AKH Wien — Vienna, Austria
• UMHAT Tsaritsa Yoanna - ISUL EAD, Pediatric clinical hematology and oncology — Sofia, Bulgaria
• Hamltn Hth Sci/McMstr Child Hosp — Hamilton, Ontario, Canada
• KBC Zagreb, Rebro, Hemofilija centar — Zagreb, Croatia
• KBC Zagreb_Hematology — Zagreb, Croatia
• KBC Zagreb, Zavod za pedijatrijsku hematologiju — Zagreb, Croatia
• Ustav Hematologie a krevni tranfuze — Prague, Czechia
• Fakultni Nemocnice Motol A Homolka — Prague, Czechia
• Skejby Blodsygdomme, blødercentret — Aarhus N, Denmark
• Hospices Civils de Lyon- Hopital Louis Pradel — Bron, France
• Centre Hospitalier de Clermont-Ferrand-Hopital Estaing — Clermont-Ferrand, France
• Ap-Hp-Hopital de Bicetre — Le Kremlin-Bicêtre, France
• Centre Hospitalier Universitaire de Rennes - Hopital Pontchaillou — Rennes, France
• Center for Inherited Blood Dis — Orange, California, United States

Full record on ClinicalTrials.gov

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