The International Generic and Biosimilar Medicines Association has appointed a veteran member, Vivian Frittelli, MBA, ACIS, to take over as chair.
The International Generic and Biosimilar Medicines Association has appointed a new chair to lead the manufacturers trade association through the coming year.
Vivian Frittelli, MBA, ACIS, the CEO of Generic and Biosimilar Medicines of Southern Africa (GBM), is taking over from Sudarhsan Jain, secretary general of the Indian Pharmaceutical Alliance. Frittelli has also served as chair of the IGBA in the past.
GBM is also a trade association representing manufacturers and distributors in pharmaceuticals in South Africa. The group has made expanding access to biosimilar and generic medicines a focus of its efforts. Biosimilars are as safe and efficacious as the brand-name products they reference.
Frittelli has roughly 25 years of experience working in the pharmaceutical industry. He formerly headed Hoffmann La Roche’s marketing and sales division in South Africa and later became country manager for Roche in Saudi Arabia. He has also served as regional director for the Smile Train, which works to bring surgical attention to children with cleft lips and palates in the Southern Africa region.
Frittelli has also worked for Sandoz Pharmaceuticals to establish their oncology division in South Africa.
IGBA has worked with the World Health Organization to reduce clinical trials requirements for biosimilar development, so that unnecessary measures of biosimilarity can be replaced by more modern, reliable means of verifying equivalence to reference products. Jain stepped into the IGBA chair role in January 2021.
“Despite these disruptive times, tangible progress was made under the WHO-IGBA Memorandum of Understanding, which allowed the IGBA submission for the WHO Non-State Actor status, which aims to increase worldwide access to affordable quality treatment,” Jain said in a statement.
Under Jain, the IGBA in 2021 published a whitepaper mapping out a blueprint for expanding generic and biosimilar access worldwide, calling for fair patenting and litigation systems, harmonized regulatory frameworks across international borders, and support for new technology and new drug development, in the form of allowances for financial support for development.
“I am very pleased to take over the Chair of IGBA for the second time and look forward to building upon the strong leadership of Sudarshan Jain,” Frittelli said.
The group also noted that Jonathan Kimball, vice president of Trade and International Affairs at the Association for Accessible Medicines, wil take over as vice chair of the IGBA. Kimball has served as vice chair of the IGBA International Trade and Intellectual Property Committee.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
Health Canada Approves First Omalizumab Biosimilar
December 16th 2024Health Canada has approved Omlyclo, the first omalizumab biosimilar in Canada, for the treatment of chronic idiopathic urticaria, allergic asthma, and chronic rhinosinusitis with nasal polyps, based on a phase 3 study confirming its bioequivalence to the reference product.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Review Confirms Clinical Safety of Sandoz Denosumab Biosimilar vs Originator
December 11th 2024Sandoz's biosimilar denosumab (Jubbonti/Wyost) has demonstrated analytical, pharmacokinetic, pharmacodynamic, and clinical equivalence to reference denosumab (Prolia/Xgeva), supporting its approval and extrapolation to all approved indications.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.