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A Clinical Trial to Evaluate Prophylactic Emicizumab Versus no Prophylaxis in Hemophilia A Participants Without Inhibitors (HAVEN3)
A Clinical Trial to Evaluate Prophylactic Emicizumab Versus no Prophylaxis in Hemophilia A Participants Without Inhibitors
- Hemophilia A
Trial Status:
Completed
This trial runs in
Cities
- Adelaide
- Atlanta
- Bonn
- Boston
- Bron
- Cardiff
- Detroit
- Dublin 8
- Firenze
- Gainesville
- Gdańsk
- Johannesburg
- Kashihara
- Kawasaki
- Le Kremlin-Bicêtre
- London
- Lublin
- Madrid
- Melbourne
- Milano
- Nedlands
- New York
- Osaka
- Paris
- Poznań
- San José
- Santa Monica
- Seattle
- Sendai
- Seoul
- Sevilla
- Shinjuku City
- Suginami City
- Taichung City
- Taipei City
- Warszawa
- Washington
- 横浜市
Trial Identifier:
NCT02847637 2016-000072-17, HAVEN3 BH30071
Trial Summary
This is a randomized, global, multicenter, open-label, Phase 3 clinical study in participants with severe hemophilia A without inhibitors against Factor VIII (FVIII) who are 12 years or older. The study evaluates two prophylactic emicizumab regimens versus no prophylaxis in this population with emphasis on efficacy, safety, and pharmacokinetics.
Hoffmann-La Roche
Sponsor
Phase 3
Phase
NCT02847637 , BH30071 , 2016-000072-17, HAVEN3
Trial Identifier
Emicizumab, Factor VIII (FVIII)
Treatments
Hemophilia A
Condition
Official Title
A Randomized, Multicenter, Open-Label, Phase III Clinical Trial to Evaluate the Efficacy, Safety, and Pharmacokinetics of Prophylactic Emicizumab Versus no Prophylaxis in Hemophilia A Patients Without Inhibitors
Eligibility Criteria
All
Gender
≥12 Years
Age
No
Healthy Volunteers
Inclusion Criteria
- Body weight >/= 40 kilogram (kg) at the time of screening
- Diagnosis of severe congenital hemophilia A
- Documentation of the details of prophylactic or episodic FVIII treatment and of number of bleeding episodes for at least the last 24 weeks
- Adequate hematologic function
- Adequate hepatic function
- Adequate renal function
- For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods that result in a failure rate of less than (<) 1 percent (%) per year during the treatment period and for at least 5 elimination half-lives (24 weeks) after the last dose of study drug
Exclusion Criteria
- Inherited or acquired bleeding disorder other than hemophilia A
- Previous or current treatment for thromboembolic disease or signs of thromboembolic disease
- Conditions that may increase risk of bleeding or thrombosis
- History of clinically significant hypersensitivity associated with monoclonal antibody therapies or components of the emicizumab injection
- Known human immunodeficiency virus (HIV) infection with cluster of differentiation (CD) 4 count <200 cells per microliter (cells/mcL) within 24 weeks prior to screening. Participants with HIV infection who has CD4 greater than (>) 200 and meet all other criteria are eligible
- Use of systemic immunomodulators at enrollment or planned use during the study, with the exception of anti-retroviral therapy
- Participants who are at high risk for thrombotic microangiopathy (TMA) (for example, have a previous medical or family history of TMA), in the investigator's judgment
- Concurrent disease, treatment, or abnormality in clinical laboratory tests that could interfere with the conduct of the study, may pose additional risk, or would, in the opinion of the investigator, preclude the participant's safe participation in and completion of the study
- Planned surgery (excluding minor procedures) during the study
- Receipt of emicizumab in a prior investigational study; an investigational drug to treat or reduce the risk of hemophilic bleeds within 5 half-lives of last drug administration; a non-hemophilia-related investigational drug concurrently, within last 30 days or 5 half-lives, whichever is shorter
- Pregnant or lactating, or intending to become pregnant during the study
For the latest version of this information please go to www.forpatients.roche.com