Earlier this month, pharmacy benefit managers (PBMs) were called before the Senate Finance Committee to answer questions about how their businesses impact drug prices for Americans. While the executives deflected criticism and pointed to issues like legal challenges to biosimilars as playing a key role in keeping drug prices high, lawmakers and officials are taking steps to rein in PBMs.
Earlier this month, pharmacy benefit managers (PBMs) were called before the Senate Finance Committee to answer questions about how their businesses impact drug prices for Americans. While the executives deflected criticism and pointed to issues like legal challenges to biosimilars as playing a key role in keeping drug prices high, lawmakers and officials are taking steps to rein in PBMs.
This week, Representative Peter Welch, D-Vermont, announced 2 new bills targeting PBMs’ practices. The first bill would prevent PBMs from imposing retroactive fees on pharmacy drug sales, while the second would prohibit PBMs from excluding small, independent pharmacies from joining preferred pharmacy networks that fill prescriptions for Medicare beneficiaries.
According to Welch, these bills will address 2 significant threats to local pharmacies to help ensure fair competition and keep small pharmacies in business.
Separately, Dave Yost, attorney general of the state of Ohio, has filed a lawsuit against the PBM OptumRx.
According to the complaint, filed in Franklin County, Ohio, OptumRx, which served as the Ohio Bureau of Workers Compensation (BWC)’s PBM from 2009 to October 2018, breached its contract with the state. The breaches alleged include failure to provide a guaranteed discount on generic drug prices, resulting in nearly $16 million in damages, and making misrepresentations to the state in order to be selected as its PBM.
The complaint explains that, in 2009, the BWC sought to enter into a pass-through contract with a PBM, in which the selected PBM would receive only administrative fees for its transactions conducted on behalf of the BWC. In such an arrangement, the PBM would be obligated to pass through the costs of drugs without markup, eliminating the possibility of spread pricing or rebates.
“Deprived of the opportunity to ramp up profits,” says the complaint, the PBM “found another way to add to its bottom line at the expense of BWC—by failing to provide the promised and agreed to pricing discounts for drugs purchased by BWC claimants.”
The complaint explains that OptumRx did not comply with its contractual duty to provide minimum average discounts of 74% off average sales price to BWC, as determined by an independent consultant hired to examine compliance. When BWC threatened to terminate the contract, OptumRx amended the contract. According to the BWC, the PBM then failed to meet its obligations under the amendment. Later, the PBM also increased the prices of drugs without explanation.
“When challenged by BWC about its failure to abide by the [agreement],” reads the complaint, OptumRx “tellingly, did not deny BWC’s obligations…instead Defendant admitted it had breached the agreement.”
Ohio is seeking a trial by jury and has asked for compensatory damages, punitive damages, all costs of litigation, and other relief the court deems to be appropriate.
In a statement, Yost said that the state’s review of PBM practices is ongoing and called this lawsuit “the first raindrops” in a coming storm.
Targeted Reimbursement Encourages Oncology Biosimilar Use
May 7th 2025Incentivizing physicians with modest financial bonuses may seem like a small step, but in Japan’s outpatient oncology setting, it helped push trastuzumab biosimilars toward broader adoption, demonstrating how even limited reimbursement reforms can reshape prescribing behavior under the right conditions.
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."
Samsung Bioepis Report Signals Turning Point for US Biosimilars
May 1st 2025A wave of biosimilar approvals, aggressive pricing strategies, and a regulatory sea change are setting the stage for unprecedented momentum in the US biologics market, with 2025 already proving to be a landmark year in reshaping cost, access, and innovation across therapeutic areas.
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?
Biosimilar Market Development Requires Strategic Flexibility and Global Partnerships
April 29th 2025Thriving in the evolving biosimilar market demands bold collaboration, early global partnerships, and a fresh approach to development strategies to overcome uncertainty and drive future success.
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.