The purpose of this study is to find out whether upfront emapalumab treatment can help in sAA (Aplastic Anemia) treatment planning and increase the effectiveness of standard treatment options. Funding Source- FDA OOPD
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
35
Emapalumab is an interferon gamma (IFNγ) blocking antibody
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York, United States
RECRUITINGCincinnati Children's Hospital Medical Center (Data collection only)
Cincinnati, Ohio, United States
RECRUITINGChildren's Hospital of Philadelphia (Data Collection AND Specimen Analysis)
Best Response
The primary objective of the study is to assess the efficacy of early upfront emapalumab on hematologic recovery within 6 weeks of starting therapy after a new diagnosis of Aplastic Anemia. Response will be determined by blood count.
Time frame: 6 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Philadelphia, Pennsylvania, United States
Virginia Commonwealth University (Data Collection Only )
Richmond, Virginia, United States
RECRUITINGChildren's Hospital of Wisconsin (Data Collection Only)
Milwaukee, Wisconsin, United States
RECRUITINGMedical College of Wisconsin (Data Collection AND Data Analysis)
Milwaukee, Wisconsin, United States
NOT_YET_RECRUITING