Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Buffy coat-derived granulocyte transfusion is a blood component therapy used to treat or prevent life-threatening infections in patients with severe, prolonged neutropenia, such as those undergoing induction chemotherapy for acute myeloid leukemia (AML). Unlike apheresis-derived granulocytes, which are collected from a single donor using a cell separator, buffy coat-derived granulocytes are prepared from the buffy coat layer of standard whole blood donations. Each unit typically contains a lower dose of granulocytes (approximately 1 x 10⁹ per bag) compared to apheresis units, often requiring multiple units to achieve a therapeutic dose. The therapy aims to provide functional neutrophils to bridge the period of marrow aplasia, thereby reducing the incidence of severe bacterial and fungal infections.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on buffy coat-derived granulocyte transfusion.