Feature

Humira biosimilars: Five things to know


 

Will patients pay less?

Biosimilars have been touted as a potential solution to lower spending on biologic drugs, but it’s unknown if patients will ultimately benefit with lower out-of-pocket costs. It’s “impossible to predict” if the discount that third-party payers pay will be passed on to consumers, said Mark Fendrick, MD, who directs the University of Michigan Center for Value-based Insurance Design in Ann Arbor.

Dr. A. Mark Fendrick, Director V-BID, University of Michigan Michigan Medicine

Dr. Mark Fendrick

Generally, a consumer’s copay is a percentage of a drug’s list price, so it stands to reason that a low drug price would result in lower out-of-pocket payments. While this is mostly true, Humira has a successful copay assistance program to lower prescription costs for consumers. According to a 2022 IQVIA report, 82% of commercial prescriptions cost patients less than $10 for Humira because of this program.

To appeal to patients, biosimilar companies will need to offer similar savings, Dr. Fendrick added. “There will be some discontent if patients are actually asked to pay more out-of-pocket for a less expensive drug,” he said.

All eight companies behind these biosimilars are offering or will be launching copay saving programs, many which advertise copays as low as $0 per month for eligible patients.

How will Humira respond?

Marta Wosińska, PhD, a health care economist at the Brookings Institute, Washington, predicts payers will use these lower biosimilar prices to negotiate better deals with AbbVie, Humira’s manufacturer. “We have a lot of players coming into [the market] right now, so the competition is really fierce,” she said. In response, AbbVie will need to increase rebates on Humira and/or lower its price to compete with these biosimilars.

“The ball is in AbbVie’s court,” she said. “If [the company] is not willing to drop price sufficiently, then payers will start switching to biosimilars.”

Dr. Fendrick reported past financial relationships and consulting arrangements with AbbVie, Amgen, Arnold Ventures, Bayer, CareFirst, BlueCross BlueShield, and many other companies. Dr. Wosińska has received funding from Arnold Ventures and serves as an expert witness on antitrust cases involving generic medication.

A version of this article first appeared on Medscape.com.

Pages

Recommended Reading

Researchers seek to understand post-COVID autoimmune disease risk
MDedge Dermatology
FDA puts partial hold on investigational alopecia areata drug deuruxolitinib
MDedge Dermatology
FDA approves autoinjector pen for Humira biosimilar, Cyltezo
MDedge Dermatology
FDA approves Yuflyma as ninth adalimumab biosimilar
MDedge Dermatology
ILD risk elevated in RA, PsA after starting biologic or targeted synthetic DMARDs
MDedge Dermatology
Is ChatGPT a friend or foe of medical publishing?
MDedge Dermatology
Why not both? Dual biologics for treatment-resistant RA and PsA
MDedge Dermatology
After Yusimry’s steep discount, little clarity on future adalimumab biosimilar pricing
MDedge Dermatology
Methotrexate does not impair sperm quality, small study finds
MDedge Dermatology
Does colchicine have a role in treating excess ASCVD risk in patients with chronic inflammatory conditions?
MDedge Dermatology