Fact CheckerSign in

NCT04563520RecruitingPhase 3

SAFE Study: Safety of aPCC Following Emicizumab Prophylaxis

aPCC and Emicizumab Safety Study in Congenital Hemophilia A Patients With Inhibitors (SAFE Study: Safety of aPCC Following Emicizumab Prophylaxis)

Source: ClinicalTrials.gov · Last updated 21 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
5 (estimated)
First submitted
21 Sept 2020
Start date
Sept 2026
Primary completion date
Mar 2027
Lead sponsor
Emory University
Diseases
Haemophilia
NCT number
NCT04563520

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 5
  • From Sept 2026 to the primary completion date, Mar 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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
  • If the patient is treated with rFVIIa or aPCC seven days before screening
  • Had current use of any medication other than emicizumab that could affect the coagulation system.
  • Participants who are at high risk for TMA (for example, have a previous medical/family history of TMA), in the investigator's judgment

Other illness

  • Inherited or acquired bleeding disorder other than hemophilia A excluding low VWF (\>30% VWF:RCo or VWF:GP1bm)
  • Conditions that may increase the risk of bleeding or thrombosis
  • History of clinically significant hypersensitivity associated with monoclonal antibody therapies or components of the emicizumab injection

Lab values

  • Known HIV infection with CD4 count \<200 cells/µL within 24 weeks before screening. Testing is not required if \<35 years of age.
  • Concurrent disease, treatment, or abnormality in clinical laboratory tests that could interfere with the conduct of the study, may pose an additional risk, or would, in the opinion of the investigator, preclude the participant's safe participation in and completion of the study

Other

  • Use of systemic immunomodulators at enrollment or planned use during the study

Who the study is looking for

  • 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)

Age in the registry: 6 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Children's Healthcare of Atlanta
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Emory University Hospital
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.