NXT007 vs Emicizumab for Hemophilia A
(ZEBRHA 2 Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests two treatments, NXT007 (an experimental treatment) and emicizumab (a medication), to determine which is more effective and safer for people with hemophilia A. Hemophilia A is a condition where blood doesn't clot properly, causing frequent bleeding episodes. The study targets individuals with severe or moderate hemophilia A or any severity with certain inhibitors that hinder clotting factor activity. Participants will either continue their current treatment or switch to a new one to help prevent bleeding. Those with hemophilia A experiencing regular bleeding issues might find this trial suitable. As a Phase 3 trial, it represents the final step before FDA approval, offering access to potentially groundbreaking treatment.
Do I have to stop taking my current medications for the trial?
The trial does not specify if you need to stop taking your current medications, but you cannot use systemic immunomodulators (medications that affect the immune system) during the study, except for antiretroviral therapy for HIV.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that NXT007, a new treatment for hemophilia A, has been well tolerated in studies. Previous research found it generally safe at different doses, with no major safety concerns reported, such as blood clots.
Emicizumab, the treatment to which NXT007 is being compared, has a well-established safety record. The FDA has already approved it for people with hemophilia A, indicating it has passed safety tests for this condition.
Both treatments appear safe based on existing research. However, joining a trial is a personal decision, and discussing any concerns with a doctor is important.12345Why are researchers excited about this trial's treatments?
Unlike the standard treatment for Hemophilia A, which often involves regular injections of clotting factor replacements, NXT007 works by mimicking the action of a natural protein that helps blood clot. This new mechanism could offer more consistent protection against bleeding episodes. Researchers are excited about NXT007 because it may reduce the frequency of treatments compared to traditional approaches, promising a simpler and potentially more effective management of the condition.
What evidence suggests that this trial's treatments could be effective for hemophilia A?
This trial will compare NXT007 with Emicizumab for treating hemophilia A. Research has shown that NXT007 could be beneficial for this condition. Early results suggest it might help control bleeding, even in patients with factor VIII inhibitors. NXT007 is designed to mimic factor VIII, which is either absent or malfunctioning in people with hemophilia A. Initial studies found that NXT007 is generally well tolerated and may significantly reduce bleeding. Emicizumab, which participants in this trial may also receive, is already known to be effective and well tolerated for hemophilia A across different patient groups. These findings suggest that both treatments could effectively manage hemophilia A.16789
Who Is on the Research Team?
Clinical Trials
Principal Investigator
Hoffmann-La Roche
Are You a Good Fit for This Trial?
This trial is for people age 12 and older with hemophilia A—either severe or moderate cases (with or without factor VIII inhibitors), or mild cases if they have chronic inhibitors. Participants must have records of recent treatments and bleeding episodes, and be willing to switch to regular preventive treatment if needed.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive either NXT007 or Emicizumab prophylaxis during the main study treatment period
Open-label extension
Participants may continue with NXT007 dosing or switch from Emicizumab to NXT007
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Emicizumab
- NXT007
Trial Overview
The study compares two preventive treatments for hemophilia A: a new drug called NXT007 versus an existing one, Emicizumab. Participants are randomly assigned to receive either medication as ongoing prophylaxis to help prevent bleeding episodes.
How Is the Trial Designed?
3
Treatment groups
Experimental Treatment
Active Control
After the main study treatment period, participants in the NXT007 arm will be able to continue with NXT007 dosing, and participants in the Emicizumab arm will be able to switch to NXT007, in the open-label extension period.
Participants randomized to this arm will receive NXT007 prophylaxis for the main study treatment period.
Participants randomized to this arm will receive emicizumab prophylaxis for the main study treatment period at 3 mg/kg once weekly (QW) for 4 weeks as loading doses, followed by maintenance dosing of either 1.5 mg/kg QW, 3 mg/kg once every 2 weeks (Q2W), or 6 mg/kg once every 4 weeks (Q4W). Loading doses are not required for participants who were taking emicizumab prior to study start.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Hoffmann-La Roche
Lead Sponsor
Dr. Levi Garraway
Hoffmann-La Roche
Chief Medical Officer since 2019
MD from the University of Basel
Dr. Thomas Schinecker
Hoffmann-La Roche
Chief Executive Officer since 2023
PhD in Molecular Biology from New York University
Chugai Pharmaceutical
Industry Sponsor
Dr. Osamu Okuda
Chugai Pharmaceutical
Chief Executive Officer since 2020
MD from Kyoto University
Dr. Mariko Y. Momoi
Chugai Pharmaceutical
Chief Medical Officer
MD from Jichi Medical University
Citations
1.
ashpublications.org
ashpublications.org/blood/article/146/Supplement%201/302/550346/NXT007-prophylaxis-in-people-with-hemophilia-ANXT007 prophylaxis in people with hemophilia A with or ...
At data cut-off, 6/7 (85.7%) pts in cohort 1 had experienced a total of 47 AEs; 8/9 (88.9%) pts in cohort 2 had 26 AEs; and 5/6 (83.3%) pts in ...
Next-generation FVIIIa-mimetic bispecific antibody NXT007
Emicizumab is well tolerated and effective in people with congenital hemophilia A regardless of age, severity of disease, or inhibitor status: a scoping review.
A first-in-human study of NXT007, a next-generation ...
Emicizumab is well tolerated and effective in people with congenital hemophilia A regardless of age, severity of disease, or inhibitor status: a scoping ...
NXT007 Suggests Favorable Tolerability and Efficacy in ...
NXTAGE Part C suggested favorable tolerability in people with hemophilia A with or without factor VIII inhibitors when switching from ...
5.
ashpublications.org
ashpublications.org/blood/article/147/19/2261/566441/NXTAGE-a-phase-1-2-study-of-NXT007-to-assessNXTAGE: a phase 1/2 study of NXT007 to assess safety ...
Managing surgery in hemophilia with recombinant factor VIII Fc and factor IX Fc: data on safety and effectiveness from phase 3 pivotal studies.
NXTAGE: a phase 1/2 study of NXT007 to assess safety ...
NXT007 had a tolerable safety profile at all doses assessed and demonstrated the potential to provide nonhemophilic coagulation activity. Abstract. NXT007 is a ...
7.
genentech-clinicaltrials.com
genentech-clinicaltrials.com/en/trials/Hemophilia/hemophilia-a/a-study-to-evaluate-the-safety--tolerability--pharmacok-88545.htmlClinical Study/NXT007-01 | ForPatients-Roche
A clinical trial to look at how safely and how well NXT007 works at different doses in people with hemophilia A – and to understand how the body processes.
8.
bleeding.org
bleeding.org/news/trial-data-for-roche-investigational-subq-hemophilia-therapy-presented-at-isthTrial Data for Roche Investigational SubQ Hemophilia ...
NXT007 is an investigational bispecific antibody therapy for people with hemophilia A who do not have factor VIII inhibitors.
A Clinical Study to Evaluate the Effects of NXT007 ...
The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics and pharmacodynamics of NXT007 prophylaxis compared with Factor VIII (FVIII) ...
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