Immuno-Oncology Drug, AM0010, Is Effective in Treating Advanced Pancreatic Cancer
New clinical trial research presented at the European Society for Medical Oncology 19th World Congress on Gastrointestinal Cancer suggests that ARMO BioSciences’ immuno-oncology drug, AM0010, is effective in treating patients with advanced pancreatic cancer.
COPD Exacerbations May Lead to Increased Risk of Heart Attack and Stroke in CVD Patients
Those with chronic obstructive pulmonary disease (COPD) may be more likely to suffer from a heart attack or stroke following an acute exacerbation if they have a history or at risk of cardiovascular disease (CVD).
Protect Against Skin Cancer by Avoiding Common Sunscreen Mistakes
With the Fourth of July quickly approaching, many people are planning to spend time outside under the sun. Sunscreen is necessary for this time of year to protect against the sun’s harmful rays; however, it is only effective if it is used properly.
Study Investigates Treatment Trends in COPD and Asthma–COPD Overlap Patients
While treatments prescribed for people with chronic pulmonary disease (COPD) and asthma—COPD overlap syndrome (ACOS) are similar, there is a need for a clearer therapeutic approach for patients with ACOS, according to a new study.
US Multi-Society Task Force's New Colorectal Cancer Screening Recommendations
The US Multi-Society Task Force recently released new recommendations for colorectal cancer (CRC) screenings. Since there has been an increase in CRC among younger Americans, while incidences in those over age 50 is decreasing, the recommendations consider the importance of systematic screening tests even for people without any CRC symptoms.
FDA Approves Rituxan Hycela for Treating Certain Blood Cancers
The FDA has approved Genentech’s Rituxan Hycela for subcutaneous injection for the treatment of certain blood cancers. Rituxan Hycela has similar outcomes as Rituxan, but can be delivered in 5 to 7 minutes compared with 1.5 hours for Rituxan.
Genentech's Ocrevus Reduces Disease Progression in Multiple Sclerosis Patients
A phase 3 clinical trial of patients with relapsing multiple sclerosis and primary progressive multiple sclerosis found that Ocrevus (ocrelizumab) significantly reduced disease progression, according to results released by Genentech.
FDA Approves of Darzalex Combination for Multiple Myeloma
The FDA has approved the use of Janssen Biotech, Inc’s immunotherapy Darzalex in combination with pomalidomide and dexamethasone. Darzalex is used to treat multiple myeloma patients who have previously received at least 2 therapies with lenalidomide and a proteasome inhibitor.
Family History, Mutation Location Increase Risks of Breast, Ovarian Cancers
Researchers investigating the risks of breast, ovarian, and contralateral breast cancer for mutation carriers found that family history and mutation position are important for determining cancer risk estimates, according to a study published in JAMA.
FDA Approves Baxdela for Skin Infections
The FDA has approved Baxdela, a drug intended to treat adults with acute bacterial skin and skin structure infections caused by susceptible bacteria. Baxdela is also effective in treating MRSA and against other gram-positive or gram-negative pathogens.
ICER Releases Update Due to New Evidence About PCSK9 Inhibitor Effectiveness
On June 14, 2017, The Institute for Clinical and Economic Review (ICER) added a “New Evidence Update” to the 2015 review of the comparative clinical effectiveness and value of PCSK9 inhibitors for management of high cholesterol.
WCHN Launches New Study to Investigate Link Between Diabetes and Pancreatic Cancer
On June 14, 2017, Western Connecticut Health Network (WCHN) announced its launch of a new study that will research the connection between pancreatic cancer and new-onset diabetes. This $2.7 million study will span 3 years and aims to discover a method to detect pancreatic cancer while it can still be cured.
SCOTUS Rules in Favor of Sandoz, Speeding Biosimilars to Market Sooner
The Supreme Court of the United States ruled in favor of Sandoz, on Monday, by allowing biosimilars to give notice of commercial marketing before or after FDA approval-meaning biosimilar products can be available sooner.