Pharma News

Biosimilar uptake appears to finally be on the upswing, and Biocon Biologics is betting on the sector’s future

This audio is auto-generated. Please let us know if you have feedback.

When a copycat of Amgen’s Neupogen became the first approved biosimilar in the U.S. less than a decade ago, the competitive prospect of drugs that mimicked pricey biologics appeared poised to bring down drug costs.

Matthew Erick, chief commercial officer, Biocon Biologics

Matthew Erick, chief commercial officer, Biocon Biologics

Permission granted by Biocon Biologics

 

Now, biosimilar makers are still fighting for even small slices of the patient population as the makers of branded drugs rake in the profits. For example, even as a new knockoff of AbbVie’s Humira hit the scene almost every month last year, payers often stuck with the branded product for a variety of reasons. Although Humira sales declined 32% last year, the drug stayed competitive through rebate-driven deals AbbVie struck with pharmacy benefit managers, according to a 2023 report from KFF Health News.

Still, Biocon Biologics, a subsidiary of India’s Biocon, has doubled down on its long-haul commitment to the biosimilars space. Some recent data supports that decision. According to a report from IQVIA, spending on biosimilars is expected to reach as much as $49 billion in 2027, and biosimilars for drugs like Rituxan and Avastin from Genentech and Herceptin from Roche have garnered more than 60% market share in their first three years after approval.

In 2021, the U.S. granted the first approval of an interchangeable biosimilar — the insulin glargine injection Semglee, a biosimilar of Sanofi’s Lantus — that could be substituted for the branded product at the pharmacy. Having partnered with Viatris on Semglee, Biocon Biologics in 2022 opted to purchase the company’s entire biosimilars program for more than $3 billion.

As a pure-play biosimilar maker with eight commercial products globally in diabetes, oncology and immunology, as well as upcoming programs in ophthalmology and bone health, Biocon Biologics competes with major companies that don’t give up ground easily.

“The real risk around this is when you have all the approvals and then things still don’t move. I can have the product and all the programs and launch with FDA approval, but I’m still fighting for 2%,” said Matthew Erick, chief commercial officer at Biocon Biologics. 

‘Biosimilar first’

To promote more equitable competition, Erick believes healthcare policies should grant biosimilars better market position as they launch so that prescribers and payers understand and take advantage of the potential savings.

“We need to think about a ‘biosimilar first’ program for adoption, because if biosimilars come in and the innovator just lowers their price, like you saw with Humira, and biosimilars gain zero traction, that’s not good for the future because a lot of money was spent on those biosimilars,” Erick said. “We need to [ensure] biosimilars are supported as a viable entity not to take the branded people out but … continuing to introduce competition.”

A “biosimilar first” approach would motivate clinicians to opt for the biosimilar over an originator product for new patients.


“If we have biosimilars launching, and they still stay where the innovators have 98% [of the market], I don’t think you’re going to have biosimilars very long. It’s really tough thinking about the investments around that.”

Matthew Erick

Chief commercial officer, Biocon Biologics


Erick sees progress being made on that front despite the challenges.

“From our perspective, it’s about access and affordability … [but] today, it’s very confusing to the patient,” Erick said. “In the next five to 10 years, though, it will be successful — what I’m proud of is we’re seeing more affordability, the launch of more biosimilars, and they can add a lot of value.”

Even in areas where innovative biologics have accrued monumental success, biosimilars can thrive, Erick said. For instance, GLP-1 medications for diabetes and weight loss such as Ozempic and Mounjaro play an important role in improving health outcomes, but they’re not for everyone. And insulin biosimilars like Semglee can fill a gap for patients outside the GLP-1 bubble.

“As we’re seeing the shift not only in the U.S. but elsewhere with GLP-1s, someone has to be there to help the patients who maybe don’t qualify for that product yet, or can’t afford it because it’s not covered,” Erick said. 

Source link
#Biosimilar #uptake #appears #finally #upswing #Biocon #Biologics #betting #sectors #future

Related Articles

Leave a Reply

Your email address will not be published. Required fields are marked *