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A Research Study Looking at How Safe it is to Switch From Emicizumab to Mim8 in People With Haemophilia A (FRONTIER 5)

Phase 3
Completed
Conditions
Haemophilia A
Haemophilia A With Inhibitors
Interventions
Drug: NNC0365-3769 (Mim8) PPX
Registration Number
NCT05878938
Lead Sponsor
Novo Nordisk A/S
Brief Summary

This study is looking at how safe it is to switch from emicizumab to Mim8, in people with haemophilia A. Mim8 is a new medicine that is used to prevent bleeding episodes in people with haemophilia A. Mim8 works by replacing the function of the missing clotting factor VIII (FVIII). Mim8 will be injected under the skin using a pen-injector either once every week, once every two weeks or once every month. The participants will be trained in using the pen injector. The participants can choose themselves, in collaboration with the study doctor how often they get Mim8 in this study. When the participant will get their first Mim8 injection depends on their current treatment with emicizumab. The participants will get their first Mim8 injection at Visit 2. Participants will have between 6 and 27 Mim8 injections. The total number of injections participants will have depends on their dosing frequency. The study will last for about 6-12 months. While taking part in this study, there are some restrictions about what medicine participant can use. The study doctor will tell the participants more about this. In case the participants experience bleeds, these can be treated with additional haemostatic medicine as agreed with the study doctor. Female participants cannot take part if they are pregnant, breast-feeding or plan to get pregnant during the study period.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
61
Inclusion Criteria
  1. Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study.
  2. Male or female with diagnosis of congenital haemophilia A of any severity based on medical records.
  3. Age 12 years or above at the time of signing the informed consent.
  4. Participants treated with emicizumab once-weekly (QW), once every two weeks (Q2W), or once every four weeks (Q4W) according to the label for at least 8 weeks prior to screening.
  5. Participants choosing to discontinue emicizumab treatment and switch to Mim8 QW, Q2W, or once-monthly (QM) treatment for 26 weeks from start of treatment (Visit 2).
  6. Participant and/or caregiver willingness and ability to comply with scheduled visits and study procedures, including the completion of an electronic diary and patient-reported outcomes (PRO) questionnaires.
Exclusion Criteria
  1. Participation (i.e., signed informed consent) in any interventional, clinical study, with the exception of emicizumab, with receipt of the last dose within 8 weeks (or 5 half-lives of the investigational medicinal product [IMP], whichever is longer) before screening.
  2. Any disorder, which in the investigator's opinion might jeopardise the participant's compliance with the protocol or safety, including ongoing Adverse Events (AEs) associated with emicizumab.
  3. Previous participation in this study. Participation is defined as signed informed consent.
  4. Known congenital or acquired coagulation disorders other than haemophilia A.
  5. Previous or current thromboembolic disease or events (with the exception of previous catheter associated thrombosis for which anti-thrombotic treatment is not currently ongoing) or risk of thromboembolic disease, as evaluated by investigator.
  6. Neutralising antibodies towards emicizumab have been detected or, for patients adherent to emicizumab therapy, are suspected based on clinical and laboratory assessments.
  7. Receipt of FVIII gene therapy at any time.
  8. Ongoing or planned immune tolerance induction therapy.
  9. Minor or major surgery planned to take place after screening and during the 26-week treatment period.
  10. Known or suspected hypersensitivity to study intervention, related products, any constituents of the product or to other monoclonal antibodies.
  11. Hepatic dysfunction defined as aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) greater than (>) 3 times the upper limit combined with total bilirubin >1.5 times the upper limit measured at screening.
  12. Renal impairment defined as estimated glomerular filtration rate (eGFR) lesser than or equal to (≤) 30 milliliter per minute per 1.73 square meter (mL/min/1.73 m^2) for serum creatinine measured at screening.
  13. Female who is pregnant, breast-feeding or intends to become pregnant or is of childbearing potential and not using highly effective contraceptive method.
  14. Mental incapacity, unwillingness to cooperate, or a language barrier precluding adequate understanding and cooperation.
  15. Other conditions (e.g. autoimmune disease) or laboratory abnormality that may increase risk of bleeding or thrombosis as evaluated by the investigator.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
NNC0365-3769 (Mim8) PPXNNC0365-3769 (Mim8) PPXParticipants will receive Mim8 prophylaxis (PPX) subcutaneous (s.c.) injection using a prefilled fixed dose DV3407-C1 pen-injector.
Primary Outcome Measures
NameTimeMethod
Number of treatment-emergent adverse eventsFrom Visit 2 (week 0) until week 26

Measured as count of events.

Secondary Outcome Measures
NameTimeMethod
Change in participants' treatment burden using the Hemophilia treatment experience measure (Hemo-TEM) total scoreFrom Visit 2 (week 0) until end of treatment (up to 26 weeks)

Measured as score points. Hemo-TEM measures treatment burden. The measure consists of 26 items yielding 5 domain scores and 1 total score. Domain scores (score range): Injection difficulties (0-100), physical impact (0-100), treatment bother (0-100), interference with daily life (0-100), and emotional impact (0-100). Total score ranges 0-100. Higher scores indicate greater treatment burden.

Device handling experience using the Hemophilia Device Handling and Preference Assessment (HDHPA) questionnaireVisit 8 (after 26 weeks of treatment)

Measured as percentage of participants. HDHPA measures device handling experience and device preference. The measure consists of 26 items that are reported individually. it is measures in units: Percentage of participants = the distribution of participant answers within each response category, for each of the 26 individual items.

Trial Locations

Locations (28)

Vivantes Klinikum am Friedrichshain - Innere Medizin - Angiologie und Hämostaseologie

🇩🇪

Berlin, Germany

Universitätsklinikum Bonn - Institut für Experimentelle Hämatologie

🇩🇪

Bonn, Germany

Children's Hospital Los Angeles - Endocrinology

🇺🇸

Los Angeles, California, United States

UC Denver Hemoph & Thrombo Ctr

🇺🇸

Aurora, Colorado, United States

St Joseph's Children's Hospita

🇺🇸

Tampa, Florida, United States

University of Iowa_Iowa City

🇺🇸

Iowa City, Iowa, United States

Central Michigan University

🇺🇸

Detroit, Michigan, United States

Univ Hosp Cleveland Med Ctr

🇺🇸

Cleveland, Ohio, United States

Penn State MS Hershey Med Ctr

🇺🇸

Hershey, Pennsylvania, United States

Vanderbilt U Med Ctr_Nashville

🇺🇸

Nashville, Tennessee, United States

Universitätsklinik für Innere Medizin V

🇦🇹

Innsbruck, Austria

AKH - Klin. Abt. f. Haematologie u. Haemostaseologie

🇦🇹

Wien, Austria

Cliniques universitaires Saint-Luc - Service Hématologie

🇧🇪

Bruxelles, Belgium

McMaster University

🇨🇦

Hamilton, Ontario, Canada

Hospices Civils de Lyon-Hopital Cardiologique Louis Pradel-1

🇫🇷

Bron, France

AOU Careggi Firenze

🇮🇹

Firenze, Italy

Fondazione IRCSS Ca' Granda Ospedale Maggiore Policlinico

🇮🇹

Milano, Italy

Azienda Ospedaliera di Rilievo Nazionale Santobono Pausilipon

🇮🇹

Napoli, Italy

Nara Medical University Hospital_Pediatrics

🇯🇵

Nara, Japan

Severance Hospital, Yonsei University Health System

🇰🇷

Seoul, Korea, Republic of

Gangdong Kyung Hee University Hospital

🇰🇷

Seoul, Korea, Republic of

Charlotte Maxeke Johannesburg Academic Hospital

🇿🇦

Parktown, Johannesburg, Gauteng, South Africa

Hospital Universitario La Paz

🇪🇸

Madrid, Spain

Hospital Universitario Regional de Málaga

🇪🇸

Málaga, Spain

Belfast City Hospital

🇬🇧

Belfast, United Kingdom

Arthur Bloom Haemophilia Centre

🇬🇧

Cardiff, United Kingdom

Royal Free Haemophilia Comprehensive Care Center

🇬🇧

London, United Kingdom

Royal Hallamshire Hospital

🇬🇧

Sheffield, United Kingdom

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