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FDA approves new medicine for aggressive pancreatic cancer, extending survival by 11.1 months in phase 3 trial.
Read on beckershospitalreview.com
The FDA has approved a new medication called Onivyde, developed by Ipsen, for patients with aggressive, metastatic pancreatic adenocarcinoma. This approval followed positive results from a phase 3 trial involving 770 patients. Onivyde, an infusion administered every two weeks, extended patients' survival by a median of 11.1 months compared to other treatments. Common side effects include fatigue, nausea, vomiting, decreased appetite, abdominal pain, and diarrhea. Despite being designated as an "orphan drug" by the FDA, meaning it's for rare conditions, Onivyde has shown significant efficacy in improving patient outcomes.
Continue reading at beckershospitalreview.com
The Commission on Excellence and Innovation in Health reflects on their first go-live of the South Australia Statewide Patient Reported Measures Program at The Queen Elizabeth Hospital.Read on …
Posted Feb 14, 2024 Digital Health Innovation Adoption Curve
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