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FDA approves Pentixapharm’s trial for new leukemia and myeloma treatment using targeted imaging and radiotherapy.
Pentixapharm has received FDA "Study May Proceed" approval for two IND applications, enabling a Phase I/II trial of its CXCR4-targeted theranostic approach in acute myeloid leukemia and multiple myeloma.
The trial will test PentixaFor for imaging and [⁹⁰Y]Y-PentixaTher for targeted radiotherapy as a less toxic alternative to conventional bone marrow conditioning before stem cell transplantation.
The FDA’s 30-day review confirmed the study’s safety, marking a key regulatory milestone.
The company plans to determine trial timing based on strategic priorities and resource availability.
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La FDA aprueba el ensayo de Pentixapharm para el nuevo tratamiento de la leucemia y el mieloma utilizando imágenes específicas y radioterapia.