SBIR/STTR Research Award

A prototype diagnostic for cellular fetal hemoglobin in sickle cell disease

Award identifier db8f7d3486872aa63eeb866090b168433024f57b0b2f3cffe610c6a4557ef72cAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$225,000

Program and phase

SBIR · Phase I

Award year

2014

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
MyoSyntax Corporation
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PA13-234
Topic code
NHLBI

Research abstract

DESCRIPTION (provided by applicant): Sickle cell disease is a major clinical problem in the US, France, the United Kingdom, Brazil, and in Africa, India and the Middle East. A recent study shows that the annual cost of medical care in the US for people whosuffer from sickle cell disease exceeds 1.1 billion. Sickle hemoglobin (HbS) polymerization drives the pathophysiology of this disease. Fetal hemoglobin (HbF) is present throughout fetal development and is replaced by adult hemoglobin (HbA). A major therapeutic goal in sickle cell disease is to induce high HbF levels in sickle erythrocytes. We contend that the amount of HbF per F-cell (HbF/F-cell) and the distribution of concentrations of HbF/F-cells is a critical determinant of disease severity. Existingmeasurement of hemolysate HbF concentration or the number of F-cells in blood does not measure HbF/F-cell or the distribution of HbF/F- cell in a patient blood sample. This unmet need is critical because even patients with high HbF can have severe di

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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