MOZOBIL (plerixafor) by Sanofi is cxcr4 chemokine receptor and blocks binding of its cognate ligand, stromal cell-derived factor-1α (sdf-1α). First approved in 2008.
Drug data last refreshed 21h ago · AI intelligence enriched 1w ago
MOZOBIL (plerixafor) is a small-molecule hematopoietic stem cell mobilizer approved in 2008 that blocks the CXCR4 chemokine receptor, releasing CD34+ stem cells from bone marrow into circulation. It is used to mobilize autologous stem cells prior to collection and transplantation in patients with non-Hodgkin lymphoma and multiple myeloma. The drug works by disrupting the SDF-1α/CXCR4 interaction that anchors hematopoietic stem cells to the marrow microenvironment.
Product approaching loss of exclusivity with modest Part D utilization and minimal claims volume; expect transition from growth-focused roles to lifecycle extension and generic transition planning.
CXCR4 chemokine receptor and blocks binding of its cognate ligand, stromal cell-derived factor-1α (SDF-1α). SDF-1α and CXCR4 are recognized to play a role in the trafficking and homing of human hematopoietic stem cells (HSCs) to the marrow compartment. Once in the marrow, stem cell CXCR4 can act to…
Hematopoietic Stem Cell Mobilizer
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Plerixafor in Acute Respiratory Distress Syndrome Related to COVID-19 (Phase IIb)
Study of MGTA-145 and Plerixafor in Patients With Sickle Cell Disease
Mobilization of Stem Cells With AMD3100 (Plerixafor) in Combination With G-CSF in Multiple Myeloma Patients
Plerixafor and Cemiplimab in Metastatic Pancreatic Cancer
Whole Brain Radiation Therapy With Standard Temozolomide Chemo-Radiotherapy and Plerixafor in Treating Patients With Glioblastoma
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Upgrade to Pro — $25/moMOZOBIL offers limited career growth opportunities due to its LOE-approaching lifecycle stage and minimal linked job count. Professionals joining this product should anticipate transition planning, generic defense strategies, and potential reassignment to growth-stage assets within 12-24 months.