The FDA approved nivolumab and relatlimab-rmbw (Opdualag) for some patients with advanced melanoma The U.S. Food and Drug Administration (FDA) has approved a combination of the checkpoint inhibitors nivolumab and relatlimab-rmbw (Opdualag) for...
The FDA approved olaparib for patients with breast cancer who have inherited BRCA mutations and have received prior neoadjuvant or adjuvant chemotherapy The U.S. Food and Drug Administration (FDA) has approved the PARP inhibitor...
The FDA approved nivolumab in combination with chemotherapy for use before surgery in certain patients with non-small cell lung cancer The U.S. Food and Drug Administration (FDA) has approved the immune checkpoint inhibitor...
The FDA recently approved the second cellular immunotherapy to treat certain adult patients with multiple myeloma. The U.S. Food and Drug Administration (FDA) has approved ciltacabtagene autoleucel (Carvykti) to treat adult patients with relapsed...
The FDA approved the targeted immunotherapy tebentafusp-tebn for certain adult patients with uveal melanoma. The U.S. Food and Drug Administration (FDA) has approved tebentafusp-tebn (Kimmtrak), a fusion protein that acts as an immunotherapy, for...
The FDA approved an immune checkpoint inhibitor for patients with stage IIB or IIC melanoma following surgical removal of their tumor. The U.S. Food and Drug Administration (FDA) approved the immunotherapeutic pembrolizumab (Keytruda) for...
The FDA approved a monoclonal antibody combined with chemotherapy TO TREAT certain childhood blood cancers that express the protein CD20. The U.S. Food and Drug Administration (FDA) has approved rituximab (Rituxan), in combination with...
The U.S. FDA approved a new combination of existing drugs to treat certain patients with multiple myeloma The U.S. Food and Drug Administration (FDA) approved a new combination therapy for multiple myeloma in adult...
A new drug approved by the U.S. FDA may help surgeons find cancer more easily and reduce the likelihood of leaving cancer cells behind The U.S. Food and Drug Administration (FDA) approved the imaging...
The U.S. FDA approved the first treatment for malignant perivascular epithelioid cell tumor The U.S. Food and Drug Administration (FDA) approved sirolimus protein-bound particles for injectable suspension (albumin-bound) (Fyarro) to treat adult patients with...
AACR Fellow Lewis C. Cantley, PhD, leads a national effort targeting triple-negative breast cancer and ovarian cancer with a novel drug combination.
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