A small investor who currently holds 20 shares of Allergan has filed a proposed securities class action lawsuit seeking to stop its purchase by AbbVie, according to reports.
A small investor who currently holds 20 shares of Allergan has filed a proposed securities class action lawsuit seeking to stop its purchase by AbbVie, according to reports.
In June, AbbVie announced a $63 billion transaction agreement to acquire Allergan at a 45% premium to its trading price ($188 a share).
The shareholder, Yuan Lan Swei, bought 40 shares in 2015 and sold half of them the following year, according to FiercePharma. The New Jersey lawsuit says the proxy statement detailing AbbVie’s proposed Allergan buy leaves out important shareholder info, such as cost savings and expenses. It also says any payouts given to AbbVie executives could cloud their judgement about the deal, which was assessed by analysts to be beneficial to Allergan shareholders.
According to the the report, the shareholder sued on behalf of other investors who could join the class and wants a court to delay the shareholder vote until key information is released.
Meanwhile, both senators as well as advocacy groups and unions have asked the Federal Trade Commission (FTC) to block the deal.
According to Reuters, last week the AbbVie-Allergan deal was cited in a letter to the FTC from a small group of Democratic senators. The letter was led by US presidential hopeful Senator Amy Klobuchar, D-Minnestota, and cites ongoing industry consolidation amidst an affordability crisis in prescription drugs for many Americans. Saying the problem affects 1 in 4 in the United States, the letter says, “It is more important than ever that the FTC take appropriate action to protect consumers from acquisitions that may threaten competition in drug markets, raise drug prices, or reduce patient access to essential medications.”
In addition, about a dozen advocacy groups and unions, including Public Citizen and the American Federation of Teachers, want the FTC to block the deal, and to go beyond what it usually considers when it looks at anticompetitive behavior.
Reuters reported that the groups warned that the deal could lead to a broader use of volume-based rebates or other incentives to insurers or pharmacy benefit managers; the use of such payments are one reason drugmakers have said prescription prices are high. The group also criticized Allergan for practices like attempting to transfer patents for its cyclosporine eye drops (Restasis) to a Native American tribe to protect it from patent challenges and delay market entry of less expensive generic versions.
Unions have long complained about the price of AbbVie’s brand-name Humira, which faced competition in Europe from biosimilar adalimumab for the first time in late 2018. While no adalimumab biosimilars are slated for US launches prior to 2023, the Humira maker has sought to mitigate the impact of biosimilars through the sales of novel agents.
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.
Commercial Payer Coverage of Biosimilars: Market Share, Pricing, and Policy Shifts
December 4th 2024Researchers observe significant shifts in payer preferences for originator vs biosimilar products from 2017 to 2022, revealing growing payer interest in multiple product options, alongside the increasing market share of biosimilars, which contributed to notable reductions in both average sales prices and wholesale acquisition costs.
Exploring the Biosimilar Horizon: Julie Reed's Predictions for 2024
February 18th 2024On this episode of Not So Different, Julie Reed, executive director of the Biosimilars Forum, returns to discuss her predictions for the biosimilar industry for 2024 and beyond as well as the impact that the Forum's 4 new members will have on the organization's mission.
The Rebate War: How Originator Companies Are Fighting Back Against Biosimilars
November 25th 2024Few biologics in the US have multiple biosimilar competitors, but originator biologics respond quickly to competition by increasing rebates and lowering net prices, despite short approval-to-launch timelines for biosimilars.