Pharmacy U

Updated: BC expands use of biosimilars


by Staff

PharmaCare launched the first phase of the Biosimilars Initiative on May 27, 2019 with the goal of switching patients using Enbrel®, Remicade®, and Lantus® for certain indications to their biosimilar versions by November 25, 2019. In its second phase (September 5, 2019 — March 5, 2020), the Initiative will switch patients using Remicade for gastrointestinal (GI) indications (Crohn’s disease or ulcerative colitis) to a biosimilar version. For details on the affected indications and biosimilar brands, see PharmaCare coverage changes below.

“B.C. is leading the country by promoting the widespread use of biosimilars, which have been proven to work just as safely and effectively as higher priced biologics. To date, Canada is far behind European jurisdictions,” said Adrian Dix, Minister of Health. “Biosimilars are a necessary step to ensure PharmaCare provides existing coverage for more people and funds new drugs well into the future.”

Despite clear evidence to support the use of biosimilars – highly similar versions of biologics that cost anywhere from 25% to 50% less – Canada has a significantly lower use rate for biosimilars compared to other jurisdictions, at approximately 8%. Other nations have upwards of 50 to 95%.

Bioengineered drugs, known as biologics, collectively are the single biggest expense for public drug plans and their costs continue to climb. In 2018, B.C. spent $125 million on Lantus, Enbrel and Remicade, three biologic drugs that treat chronic conditions such as diabetes, arthritis and Crohn’s disease.

About 20,400 British Columbians living with either ankylosing spondylitis, diabetes, plaque psoriasis, psoriatic arthritis or rheumatoid arthritis will have six months to work with their healthcare team to transition their prescription from the biologic to the biosimilar drug by Nov. 25, 2019. After that time, PharmaCare will no longer provide coverage for the original biologic drug for these indications, except for exceptional cases.

“We know that our use rates can be much higher. For example, the biosimilars for infliximab (known as Inflectra and Remsima) have combined 5 to 10% use rate in Canada after four years on the market, compared to Norway (98%), United Kingdom (90%) and Scotland (85%). As a result, in 2017, Canada spent over $1.1 billion on the original biologic drug called Remicade,” added Dix.

B.C. consulted with a number of stakeholders on the transition to biosimilars and received support from prescribers and patient groups, such as the rheumatologists, the BC Society of Rheumatologists, endocrinologists, Doctors of BC, Arthritis Consumer Experts, Arthritis Society, BC Pharmacy Association, Neighbourhood Pharmacy Association, regional health authorities, Health Canada, CADTH, Patented Prices Medicine Review Board and the pan-Canadian Pharmaceutical Alliance.

Roughly 2,700 Crohn’s and ulcerative colitis patients will also be transitioning to their biosimilar treatment option in the coming months. More information for gastroenterology patients will be available in summer 2019.

After the six-month transition period, PharmaCare will no longer provide coverage for the original biologic drug for these indications. By increasing the use of biosimilars, B.C. will save about $96.6 million over the first three years which will be redirected to support additional drug listings and improved patient coverage.

Effective May 27, Jardiance (empagliflozin) is now listed as a limited coverage benefit under PharmaCare. Jardiance is a type of drug known as an SGLT2 inhibitor and has been shown to be an effective treatment option to manage diabetes. Approximately 22,000 patients could stand to benefit from this listing, which will cost roughly $4.1 million this fiscal year and $18.9 million over three years.

The psoriatic arthritis drug Taltz (ixekizumab) is being added as a limited coverage benefit, and coverage criteria will be expanded for existing arthritis drugs to improve patient access. More information about improved coverage criteria is available on the PharmaCare website. These changes will help more British Columbians living with arthritis to find the treatment option that works best for them.

PharmaCare will also be broadening coverage for several drugs used for arthritis (i.e., DMARDs, certolizumab, leflunomide, rituximab, tocilizumab, and tofacitinib). These changes will improve patient access to these important medicines by, for example, reducing coverage pre-requirements and extending the coverage periods.

According to a news release from the government, this is the latest major change to improve access to prescription drugs for British Columbians. In January 2019, B.C. made a $105-million investment over three years to reduce and/or eliminate deductibles and co-payments for lower-income British Columbians. This was the first change in the Fair Pharmacare deductible structure in 15 years.

As well, B.C. held a leading role in the national Generics 2.0 agreement to lower costs of the most commonly prescribed drugs, and actively participates in the pan-Canadian Pharmaceutical Alliance to negotiate for lower drug costs for all Canadians. British Columbia will continue to work to make sure everyone can afford and receive the medication they need.