After generic entry, Zytiga’s market share fell to about 14% and monthly net sales across the entire market fell 85%.
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New analysis suggests that even with rebates, the new Alzheimer’s therapy could have implications for Medicaid drug spending.
An FDA inspection of compound pharmacy Innoveix Pharmaceuticals indicated these lots may not be sterile.
A permanent code is expected in the third quarter of 2021.
The first generic equivalent of the HIV therapeutic is now available.
The therapy for opioid-induced constipation has no restrictions on an unidentified national formulary that serves these Blues plans.
The new indication provides a subcutaneous option for multiple myeloma that can be administrated in minutes, rather than hours.
The review will determine whether there should be a national Medicare coverage policy for the Alzheimer’s therapy.
Jardiance lowered risk of hospitalization from acute kidney injury but increased risk of hospitalized from diabetic ketoacidosis compared with a DPP4 inhibitor in one interim analysis.
Commercial insurers are beginning to provide coverage information on Biogen’s controversial therapy.
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While the risk of exposure is low, it presents a severe hazard.
This is part of a larger effort by President Joe Biden to promote competition in the American economy.
The specialty pharmacy is licensed in all 50 states.
This is the eighth generic version of the drug to treat insomnia.
Orally dissolving film formulation of riluzole is now available for patients who have difficulty swallowing.
New data show efficacy in all forms of heart failure regardless of ejection fraction.
The prescribing information for Aduhelm now specifies its use in patients with a mild form of the disease.
The agency also granted tezepelumab priority review with a PDUFA date sometime in the first quarter of 2022.
The single-dose antibiotic with a one-hour infusion is approved to treat MRSA and other skin infections.
The company is transferring manufacturing of the final product to its own site in Austria.
Despite an advisory committee recommendation for approval, the FDA did not approve what would have been the first disease-modifying therapy for type 1 diabetes.
This approval comes days after Merck announced it would withdraw indication for third-line gastric cancer.
New, extended-release therapy for post-operative pain reduces the need for opioid pain relief.
The move follows an April 29 vote by the FDA Oncology Drugs Advisory Committee.
Coverage now includes 85% of commercial lives.
Formulary adoption is a key step in achieving sales pull through starting in 2022, company officials said.
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