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Saskatchewan.ca will undergo routine maintenance on October 1 from 12:30 to 5 a.m. (CST) and may be unavailable briefly during this time.
We apologize for the inconvenience and thank you for your patience.
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The Saskatchewan Biosimilars Initiative was announced to improve the uptake of biosimilar drugs.
Biosimilars present a significant opportunity for cost savings and health system sustainability while providing safe and effective medication options. The Biosimilars Initiative supports patient access to public drug coverage and new drug benefits.
The Biosimilars Initiative means that patients are covered for a biosimilar version of their biologic medication where one is available.
Several public drug plans across Canada, including Alberta, British Columbia, New Brunswick, Newfoundland and Labrador, Nova Scotia, the Northwest Territories, Ontario, Quebec and Yukon have put in place similar policies to increase uptake of biosimilar drugs. Several countries have also put in place policies to encourage the use and transition to biosimilars.
Under the Saskatchewan Biosimilars Initiative patients already using a reference biologic (or “originator” biologic) with an available biosimilar version need to start using a biosimilar version of their medication to keep their coverage under the Saskatchewan Drug Plan.
Letters have been mailed to affected patients using the following reference biologic drugs:
Drug | Letters Mailed |
Humalog (insulin lispro) | Week of October 2, 2023 |
This information will be updated as letters are mailed to affected patients using other reference biologic drugs included in the Saskatchewan Biosimilars Initiative.
You may be affected by this policy if:
To start using a biosimilar medication, you should:
In some cases, you may have the option to enrol in a biosimilar patient support program. Your health care provider can help you with this.
If you receive Saskatchewan Drug Plan coverage of a reference biologic insulin affected by the Saskatchewan Biosimilars Initiative, you will need to start using a biosimilar insulin to keep your coverage of this medication. You can start using a biosimilar insulin by getting a new prescription for a biosimilar from your physician or nurse practitioner, or by asking your pharmacist to help you transition to a biosimilar. More details for patients and health care providers.
If you also receive medication coverage from a third-party insurance provider (such as a benefits plan through your employer):
Exemptions: Some patients may need to continue using the reference biologic for medical reasons. Exemptions to the Saskatchewan Biosimilars Initiative policy may be considered for an individual patient to continue their Saskatchewan Drug Plan coverage of a reference biologic. Prescribers can submit a request and clinical information for an individual patient. The Exemption Request Form can be found in the Prescriber Forms section.
The List of drugs affected outlines the biologic drugs currently included in the Biosimilars Initiative. The Biosimilars Initiative will also apply to future reference biologics as new biosimilars are launched and listed on the Saskatchewan Formulary. Prescribers and patients will be notified of these changes in the future.
Drug Name | Reference biologic brand name (switch from) | Biosimilar brand name (switch to) | Health conditions | End of transition period |
Insulin lispro | Humalog® | Admelog® | Diabetes | March 31, 2024 |
Please note that patients will continue to be able to access Saskatchewan Drug Plan coverage of their reference biologic medication if a suitable biosimilar format is not available.
Notes
Concluded Transition Periods
Biologic drugs are made from living organisms or their cells. They differ from most other drugs in that they are not made by chemicals. Biologic drugs include hormones, blood products, antibodies, genes and vaccines. Biologics treat many different diseases, including Crohn’s and colitis, rheumatoid arthritis and diabetes.
A reference biologic or “originator” drug is the first version of a biologic drug to be made.
Biosimilar drugs are the next versions of the biologic drug to be made after the reference biologic’s patent expires. Patients and health care professionals can be confident that biosimilars are as effective and safe as reference biologics.
Biosimilars are regulated and monitored by Health Canada. Clinical studies show that biosimilars have the same efficacy and safety as the reference biologic drug.
Note: Patient Support Program information has been provided to the Saskatchewan Drug Plan by the manufacturers and may not be available for all biologic products. Please contact the Patient Support Program or drug manufacturer directly for more information, or if you have questions about these services.
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Download Biosimilars Policy Resources
Saskatchewan Biosimilars Initiative: Notice to Patients - Humalog® (insulin lispro)
Biosimilar Insulin Transition Fee (BITF) Pharmacy Policy and Billing Procedure
Letter to Health Care Providers - October 20, 2022
Letter to Health Care Providers - November 18, 2022
Letter to Health Care Providers - January 23, 2023
Letter to Health Care Providers - February 27, 2023
Letter to Health Care Providers - April 6, 2023
Letter to Health Care Providers - May 1, 2023
Letter to Health Care Providers - September 25, 2023
Patients should contact their doctor, nurse, or pharmacist with questions about their treatment or about biosimilar medications.
medSask is a drug information service available to support patients and health care providers with questions about their biologic drug treatment.
For general questions about the Saskatchewan Biosimilars Initiative, please contact the Saskatchewan Drug Plan by email: sk.biosimilars@health.gov.sk.ca or call 1-800-667-7581 (306-787-3317 in Regina)
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