SAFE Study: Safety of aPCC Following Emicizumab Prophylaxis (NCT04563520) | Clinical Trial Compass
RecruitingPhase 3
SAFE Study: Safety of aPCC Following Emicizumab Prophylaxis
United States5 participantsStarted 2026-06
Plain-language summary
The purpose of the aPCC-emicizumab safety study is to investigate the hemostatic efficacy as measured by thrombin generation, of a low personalized dose of aPCC (FEIBA) in children and adults with hemophilia A and inhibitors on emicizumab prophylaxis.
Who can participate
Age range6 Years
SexALL
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Inclusion Criteria:
* Moderately severe hemophilia A, defined as FVIII level \<0.05 IU/mL before development of an inhibitor
* Age ≥6 years of age at time of informed consent
* Documented on 2 occasions a high titer inhibitor (\>5 BU/mL) with a 72-hour washout within 2 years of enrollment
* Parent/guardian (Legally Authorized Representative) or the patient has provided written informed consent
* Adequate hematologic function (Hgb \>8 g/dL and platelet count \>100,000 µL)
* Adequate hepatic function (total bilirubin ≤1.5 x ULN and both AST/ALT ≤3x ULN at screening (excluding known Gilbert's)
* Adequate renal function (≤2.5 x ULN and CrCl ≥30 mL/min)
Exclusion Criteria:
* Inherited or acquired bleeding disorder other than hemophilia A excluding low VWF (\>30% VWF:RCo or VWF:GP1bm)
* Had an active bleed requiring factor therapy at screening
* Previous or current treatment for thromboembolic disease or signs of thromboembolic disease (excluding previously resolved line-associated thrombosis)
* Had a surgical procedure 14 days before screening
* Conditions that may increase the risk of bleeding or thrombosis
* If the patient is treated with rFVIIa or aPCC seven days before screening
* History of clinically significant hypersensitivity associated with monoclonal antibody therapies or components of the emicizumab injection
* Had current use of any medication other than emicizumab that could affect the coagulation system.
* Known HIV infection with CD4 count \<200 cells/µL within …
What they're measuring
1
Thrombin generation capacity after aPCC (FEIBA) infusion
Timeframe: Baseline and up to 30 minutes after infusion