
Report: UnitedHealth picks up healthcare payments company Equian in $3.2B deal
Indianapolis-based Equian processes more than $50o billion in healthcare claims annually and works with nine out of the top 10 healthcare payers.
Indianapolis-based Equian processes more than $50o billion in healthcare claims annually and works with nine out of the top 10 healthcare payers.
Beacon Health serves more than 40 million individuals across the country, including 3 million patients in" risk-based behavioral programs."
The planned withdrawal follows the January failure of a Phase III trial to back up the study used for Lartruvo's accelerated approval. Following the announcement, the FDA and EMA recommended no new patients receive the drug.
Through a grant to the Indiana Legal Services, Anthem has expanded access to free legal services to all Medicaid patients in 18 counties in Central Indiana to assist with housing, employment and child support issues.
The company, Olio, plans on using the funding to scale its technology, expand across the country and grow its marketing, engineering and customer success teams.
Sen. Dick Durbin, D-Illinois, was also among four signatories to a letter to FDA Commissioner Scott Gottlieb calling on the agency to speed up approvals of generic versions of insulin products.
The new version, sold under its generic name, would be priced 50 percent lower than the branded version, at $137.35 per vial or $265.20 for a five-pack of pens.
Anthem, which has nearly 40 million members, has moved up the timeline on the development and launch of its own PBM known as IngenioRx, cutting ties with Express Scripts in the process.
Lilly announced last week that the Phase III confirmatory trial for Lartruvo in soft-tissue sarcomas failed to confirm the benefit seen in the Phase II study that led to its accelerated approval.
A Phase III trial of Lartruvo, which won accelerated approval for soft-tissue sarcoma in 2016, failed to confirm an overall survival benefit.
Loxo's shares were up 65 percent on the news. The company won FDA accelerated approval on Nov. 26 for its tissue-agnostic cancer drug, Vitrakvi.
Most recently, Udi Manber has served as a healthcare researcher and faculty member at the National Institutes of Health and at UC San Francisco.
Endocyte entered its targeted radioligand therapy, Lu-PSMA-617, into a Phase III study in June following Phase II data showing more than 60 percent response rate.
The company plans to use the financing to support development of its drug, KarXT, in schizophrenia and indications like pain.
Financial terms of the deal, which expected to close in the third quarter of this year, were not disclosed.