In its second quarter earnings call, drug maker AbbVie revealed that, in the United States, Humira sales grew by $3.8 billion last quarter, up 7.7% from the prior year, with volume growth of approximately 7%.
In its second quarter earnings call, drug maker AbbVie revealed that, in the United States, Humira sales grew by $3.8 billion last quarter, up 7.7% from the prior year, with volume growth of approximately 7%.
Additionally, in the third quarter of this year, the company expects US Humira sales to grow by approximately 8%.
Furthermore, AbbVie’s spate of settlements with biosimilar developers with products referencing Humira “reinforces our confidence that we will not see direct biosimilar competition in the US until 2023,” said Rick Gonzalez, chief executive officer of AbbVie. Gonzalez also added that the company does not expect a prospective arrival of a biosimilar etanercept—2 of which are approved but unlaunched in the United States—to impact US Humira sales.
International sales of Humira, however, were down by $1.1 billion, or 31% on an operational basis, which Gonzalez said reflects “the impact of direct biosimilar competition in Europe” and other ex-US markets.
Other drivers of AbbVie’s revenue this quarter—which totaled more than $8.2 billion and exceeded expectations—were the oncology drugs ibrutinib (Imbruvica) and venetoclax (Venclexta) as well as risankizumab (Skyrizi), a treatment for plaque psoriasis.
Michael Severino, MD, executive vice president of research and development and chief scientific officer of AbbVie, added that the company expects an approval for upadacitinib shortly in the indication of rheumatoid arthritis without the convocation of an FDA advisory committee. Severino indicated that, while he cannot speak to the FDA’s position on whether JAKs as a class share similar safety concerns, such as those that led to a new warning for tofacitinib just last week, “we’ve said consistently [that] our program hasn’t demonstrated that risk.”
In looking toward the future, Gonzalez said that AbbVie’s acquisition of Allergan will give the company an opportunity to grow its non-Humira business, and to derive “significant additional earnings” when Humira faces US competition.
Overcoming Challenges to Improve Access and Reduce Costs
November 12th 2024Biosimilars hold the potential to dramatically lower health care costs and improve access to life-changing treatments, but realizing this potential will require urgent policy reforms, market competition, and better education for both providers and patients.
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.
Skyrizi Overtakes Humira: “Product Hopping” Leaves Biosimilar Market in Limbo
November 7th 2024For the first time, Skyrizi (risankizumab-rzaa) has replaced Humira (reference adalimumab) as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.
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.
Panelists Stress Stakeholder Education to Build Confidence in Biosimilars
October 31st 2024By expanding educational initiatives to clarify biosimilar safety, efficacy, and interchangeability, stakeholders can foster trust, improve access, and ensure that biosimilars are widely accepted as high-quality, cost-effective alternatives to originator biologics.