Pharmaceutical Executive
Recent events you may have missed on the global pharma scene.
Typically, news from global pharma comes from the UK, Brussels, Washington, or the NJ/PA corridor. But a recent Google search found these news nuggets from these unsung countries in pharmaceutical development-Egypt, Cuba and Prince Edward Island.
Military receives license to form a pharmaceutical company: According to a Reuters article online Jan. 22, Egyptian Prime Minister Sherif Ismail decreed its military could “partake in the founding of a company called the Egyptian
National Company for Pharmaceuticals.” The reasons are based on the country’s low currency rate, which has led to a drug shortage, inability for generic manufacturers in Egypt to purchase the active ingredients needed, and raised medicine prices due to fraying negotiations with pharma companies.“The real story is not so much Egypt’s involvement of the military as the sheer desperation of governments as they resort to drastic measures in their attempt to address the looming crisis across the globe in which access to even categories of basic, low-sophistication drugs is visibly worsening following manufacturing restructuring by the pharma industry,” said Frederic Boucheseiche, PE EAB member and senior publisher at PharmaBoardroom.com.
First American institution to offer Cuban medial therapy in clinical trials: Buffalo, N.Y.-based Roswell Park Cancer Institute received FDA authorization in October 2016 to begin offering the lung cancer treatment vaccine CIMAvax EGF® to a limited number of patients through a clinical trial. A Jan. 10 online
Marketplace.org article described how this US-Cuba connection came about, as well as the overall US-Cuba pharma atmosphere. The vaccine was developed by the government-run Center for Molecular Immunology (CIM). Roswell became the first American institution to receive FDA permission to sponsor testing of a Cuban medical therapy in the US. And while CIMAvax has already been used to treat about 4,000 patients worldwide, and is approved for use in Bosnia and Herzegovina, Colombia, Cuba, Paraguay and Peru, it could take some time before it is approved in the US.
Canadian island-based CDMO grows from garage to four locations: The Guardianreported on Jan. 7 that 45-year-old CDMO BioVectra (a Mallinkrodt Pharmaceuticals company) has plans to grow its staff and double its revenue within five years. BioVectra President Oliver Technow has been leading the
company since late 2015 and believes its customers appreciate the client-centric partnership, which is based on the Atlantic Canadian personality that “goes the extra mile.” Another plus in its Atlantic Canadian location is the proximity to several major markets and competitive costs compared to other CDMOs. The reporter also noted that BioVectra is the oldest and largest PEI-based biotechnology company and is one of over 45 business that make up the island’s bioscience cluster. Pretty impressive for an island comprising a bit over 2,000-square miles.
Lisa Henderson is Pharm Exec’s Editor-in-Chief. She can be rached at lisa-henderson@ubm.com
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.
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.