Mylan revealed in its recent fourth quarter 2018 earnings call that it had an initial advisory meeting with the FDA regarding a proposed biosimilar onabotulinumtoxinA, referencing the brand-name Botox.
Mylan revealed in its recent fourth quarter 2018 earnings call that it had an initial advisory meeting with the FDA regarding a proposed biosimilar onabotulinumtoxinA, referencing the brand-name Botox.
Mylan said that the FDA’s feedback leads it to believe that the biosimilar approval pathway is viable for this product, and that Mylan could be the first developer to commercialize a biosimilar onabotulinumtoxinA.
The originator onabotulinumtoxinA, a neuromuscular blocking agent, is approved to treat conditions including incontinence due to neurological conditions, prophylaxis of headache in patients with migraine, upper limb spasticity, cervical dystonia, and strabismus, among other indications, such as its cosmetic uses.
Mylan’s development partner for the candidate, Revance, said that successful completion of a biosimilar program could result in FDA approval for all 11 FDA-approved indications for the reference product, and Revance’s president and chief executive officer said in a recent earnings call that “we know what needs to be done, and the FDA has set the right level of expectations” for biosimilar approval.
Allergan and Medytox, makers of the brand-name Botox, face a recent competitor, the recently FDA-approved prabotulinumtoxinA-xvfs, marketed as Jeuveau. Despite being a purified botulinum toxin type A, like the innovator Botox, the newly authorized product was submitted to the FDA under a new Biologics License Application, and was not treated as a biosimilar of the innovator Botox. Its developer, Evolus, in partnership with drug maker Daewoong, sought only indications for the product’s aesthetic use, and the product is not approved for medical indications.
Allergan and Medytox are hoping to block Jeuveau’s sales in the United States; the companies filed a complaint with the US International Trade Commission in which they asked for an investigation into Evolus’ manufacturing of botulinum toxin products. While details of the complaint are confidential, Bloomberg reported that Allergan and Medytox have alleged that the rival product was developed using manufacturing secrets stolen by an Evolus employee.
Allergan and Medytox seek an immediate investigation into whether the product was developed, made, or imported using stolen secrets, and ask for Evolus to be prohibited from selling the drug in the United States.
Eye on Pharma: Keytruda Biosimilar Deal; German Court Bans Imraldi; New Biosimilars for Japan
June 17th 2025Alvotech and Dr. Reddy's partner to develop a Keytruda biosimilar, a German court bans Humira biosimilar over patent dispute, and Samsung Bioepis enters a strategic agreement with NIPRO Corporation in Japan.
Escaping the Void: All Things Biosimilars With Craig & G
May 4th 2025To close out the Festival of Biologics, Craig Burton and Giuseppe Randazzo from the Association for Accessible Medicines and the Biosimilars Council tackle the current biosimilar landscape and how the industry can emerge from the "biosimilar void."
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?
Eye on Pharma: Interchangeability Labels and Expanded Biosimilar Partnerships
May 29th 2025The FDA designates 2 biosimilars as interchangeable, enhancing access to treatments for inflammatory diseases and multiple sclerosis, while 2 other companies expand their biosimilar partnership to include more products.