Daratumumab Combo Meets Primary End Point in Relapsed/Refractory Multiple Myeloma
August 3rd 2020The study is evaluating the subcutaneous formulation of daratumumab in combination with pomalidomide and dexamethasone versus pomalidomide and dexamethasone alone as treatment for patients with relapsed or refractory multiple myeloma.
Back on the Books Initiative Launched to Aid in Rescheduling Cancer Screening Appointments
July 31st 2020The goal of the initiative is to have cancer screenings that were made in the first half of 2020 and cancelled due to COVID-19 rescheduled to ensure patients are again receiving routine screenings.
Global Lung Cancer Burden Suggests Need for Tailored Measures
July 31st 2020Researchers suggested that based on their findings, increased efforts are needed to implement intervention strategies tailored to local settings to effectively decrease the global lung cancer burden and reduce health inequality.
FDA Grants Breakthrough Therapy Designation for Pevonedistat to Treat Higher-Risk MDS
July 30th 2020Takeda Pharmaceutical Company Limited announced the FDA granted pevonedistat, its investigation NEDD8-activating enzyme inhibitor, breakthrough therapy designation to treat patients with higher-risk myelodysplastic syndrome.
FDA Grants Breakthrough Therapy Designation to Osimertinib for Early-Stage EGFR+ NSCLC
July 30th 2020The FDA granted breakthrough therapy designation to osimertinib for the adjuvant treatment of patients with early-stage epidermal growth factor receptor-mutated non-small cell lung cancer after complete tumor resection with curative intent.
FDA Grants Breakthrough Therapy Designation, Orphan Drug Designation to MK-6482
July 29th 2020The FDA granted breakthrough therapy designation to MK-6482 for the treatment of patients with von Hippel-Lindau disease-associated renal cell carcinoma and orphan drug designation to MK-6482 for von Hippel-Lindau disease.
FDA Grants Fast Track Designation to BDTX-189 to Treat Allosteric HER2 or EGFR Mutations
July 28th 2020Black Diamond Therapeutics announced that the FDA granted fast track designation to BDTX-189 for the treatment of adult patients with solid tumors harboring an allosteric HER2 mutation or an EGFR or HER2 Exon 20 insertion mutation.
Oral Apixaban May Be Safe Alternative to Subcutaneous Enoxaparin for Thromboprophylaxis
July 27th 2020Within this study, satisfaction was markedly higher in those treated with apixaban, and adherence rates appeared to be similar between both modalities in women undergoing surgery for gynecologic cancer.
Hospice Video Educational Tool Shows Promise for Patients with Advanced Cancer and Their Caregivers
July 24th 2020Though the video did not have a statistically significant impact, those assigned to watch the video appeared to be more informed about hospice care and reported more favorable perceptions of hospice.