This week, drug maker Sanofi filed a patent infringement suit against Mylan in a New Jersey district court. Sanofi’s suit alleges that Mylan has infringed on 18 patents for its originator insulin glargine, Lantus.
This week, drug maker Sanofi filed a patent infringement suit against Mylan in a New Jersey district court. Sanofi’s suit alleges that Mylan has infringed on 18 patents for its originator insulin glargine, Lantus.
The suit was triggered by Mylan’s filing of a New Drug Application (NDA) with the FDA for a pre-filled pen and a drug vial presentation of a follow-on insulin glargine (in the United States, insulins are regulated as drugs and not as biologics; hence, drug makers must submit NDAs rather than biologics license applications for follow-ons of originator products). According to Sanofi, the Mylan NDA included a challenge to all of Sanofi’s patents listed for Lantus in the FDA’s orange book.
Mylan’s filing of an NDA for its proposed insulin glargine follows the recent release of data demonstrating comparable efficacy, safety, and immunogenicity with Lantus, as well as the follow-on’s pharmacokinetic and pharmacodynamic equivalence with the reference drug. Mylan, working together with India-based partner Biocon, is also seeking European approval for its product; in September, Biocon received a certificate of compliance from the European Union for its manufacturing facility in Malaysia where it plans to produce the insulin. Approval of the facility was welcome news for Biocon; high operational costs related to the Malaysian facility had been partially responsible for a 51% drop in Biocon’s second-quarter net profits, despite the company’s strong sales of insulins.
Sanofi faces challenges from other drug developers who seek a share of the Lantus market; in July, the FDA granted Merck’s follow-on insulin glargine a tentative approval, but will not provide the drug with a final approval until patent litigation, brought by Sanofi, has concluded. Sanofi’s suit triggered an automatic stay of 30 months.
Already on the US market is Boehringer Ingelheim’s (BI) Basaglar, the first FDA-approved insulin glargine follow-on, which launched in 2016 after a lengthy patent litigation with Sanofi. Competition from Basaglar led to steep declines in insulin market share for Sanofi in the second quarter of 2017; Sanofi’s US sales of Lantus and Toujeo (a second insulin glargine) dropped by 23.9%. CEO Oliver Brandicourt has alerted investors that the company’s fortunes were unlikely to change in the remainder of 2017, and warned that the company could see accelerated declines in sales of its insulins as it faced further competition.
Eye on Pharma: Sandoz Files Antitrust Suit; Yuflyma Interchangeability; Costco’s Ustekinumab Pick
April 22nd 2025Sandoz's antitrust suit against Amgen, the FDA’s interchangeability designation for Celltrion’s adalimumab biosimilar, and the inclusion of an ustekinumab biosimilar in Costco’s prescription program highlight growing momentum to expand biosimilar access and affordability for patients with chronic inflammatory diseases.
How AI Can Help Address Cost-Related Nonadherence to Biologic, Biosimilar Treatment
March 9th 2025Despite saving billions, biosimilars still account for only a small share of the biologics market—what's standing in the way of broader adoption and how can artificial intelligence (AI) help change that?
President Trump Signs Executive Order to Bring Down Drug Prices
April 16th 2025To help bring down sky-high drug prices, President Donald Trump signed an executive order pushing for faster biosimilar development, more transparency, and tougher rules on pharmacy benefit managers—aiming to save billions and make meds more affordable for everyone.
Will the FTC Be More PBM-Friendly Under a Second Trump Administration?
February 23rd 2025On this episode of Not So Different, we explore the Federal Trade Commission’s (FTC) second interim report on pharmacy benefit managers (PBMs) with Joe Wisniewski from Turquoise Health, discussing key issues like preferential reimbursement, drug pricing transparency, biosimilars, shifting regulations, and how a second Trump administration could reshape PBM practices.
Latest Biosimilar Deals Signal Growth Across Immunology, Oncology Markets
April 14th 2025During Q1 2025, pharmaceutical companies accelerated biosimilar expansion through strategic acquisitions and partnerships in hopes of boosting patient access to lower-cost treatments in immunology and oncology.
Experts Pressure Congress to Remove Roadblocks for Biosimilars
April 12th 2025Lawmakers and expert witnesses emphasized the potential of biosimilars to lower health care costs by overcoming barriers like pharmacy benefit manager practices, limited awareness, and regulatory delays to improve access and competition in chronic disease management during a recent congressional hearing.