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FDA Approves Addition of Survival Data to Kyprolis Label for Multiple Myeloma Treatment
June 12th 2018The Food and Drug Administration (FDA) approved the supplemental New Drug Application to add to the U.S. Prescribing Information for Kyprolis (carfilzomib) for the treatment of patients with relapsed or refractory multiple myeloma.
Specialized Care Is Needed for Adolescent and Young Adult Cancer Survivors
June 11th 2018The survey contained questions on a range of issues they may have experienced, including pain, fatigue, as well as issues with sexual function, body image and finances. Researchers then looked at the anxiety and depression associated with those issues, and talked with patients about what they thought might be causing those problems.
Patients With Myeloma Precursor Report Worse Quality of Life
June 8th 2018Cancer affects many aspects of a person’s life, such as the overall quality of their day-to-day living, but what if a person didn’t have the full-blown disease already? Could a precursor or asymptomatic stage of the disease still burden them?
Venclexta Combination Receives Full FDA Approval for CLL, With or Without 17p deletion
June 8th 2018The Food and Drug Administration (FDA) approved Venclexta (venetoclax) in combination with Rituxan (rituximab) for the treatment of patients with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL), with or without the genetic mutation 17p deletion, who have received at least one prior therapy.
FDA Approves Leukine to Treat Blood-Related Acute Radiation Syndrome
June 6th 2018The Food and Drug Administration (FDA) approved Leukine (sargramostim) for the treatment of adult and pediatric patients who are exposed to myelosuppressive doses of radiation that results in a hematopoietic subsyndrome of acute radiation syndrome.