In an effort to ensure access to certain widely used drugs at affordable prices, a group of leading hospitals and health systems have established a not-for-profit organization to produce therapies in short supply or subject to unusual price increases. Industry veteran Martin van Trieste, former chief quality officer for Amgen, was named CEO of Civica Rx, lending credibility to this much-anticipated plan.
An initial proposal for a provider-based system to counter rocketing drug prices and serious shortages was announced in January 2018. Since then it has attracted more than 120 health organizations, including Catholic Health Initiatives, HCA Healthcare, Intermountain Healthcare, Mayo Clinic and Providence St. Joseph Health; these and others together represent more than one-third of the nation’s hospitals. The venture has received $30 million in funding from a number of foundations and investors and aims to raise $200 million to support the operation.
The plan is to initially produce 14 hospital-administered generic drugs through contract manufacturers or generic drug makers with FDA-approved facilities, with the aim of bringing an initial product to market by early 2019. Van Trieste, who had recently retired and is heading the venture with no salary, expects the venture to bring “much needed competition to the generic drug market.”
An unknown is how current manufacturers will respond to this operation, perhaps by reducing prices or boosting production. Many short-supply therapies are sterile injectables, which raise production challenges. But hospitals anticipate that access to more reliable supplies will be important in reducing the time and effort now needed to track supplies, seek out alternatives, and advise health workers on the need to vary prescribing and drug administration practices.
What Every Pharma CEO Should Know About Unlocking the Potential of Scientific Data
December 11th 2024When integrated into pharmaceutical enterprises, scientific data has the potential to drive organizational growth and innovation. Mikael Hagstroem, CEO at leading laboratory informatics provider LabVantage Solutions, discusses how technology partners add significant value to pharmaceutical R&D, in addition to manufacturing quality.
FDA Approves Hikma’s Generic GLP-1 Agonist for Type 2 Diabetes
December 24th 2024Approval marks the first generic version of liraglutide injection, referencing Victoza, for improving glycemic control in adults and children aged 10 years and older with type 2 diabetes, alongside diet and exercise.
Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.