Senate Bill 6569 (Out-of-Pocket Task Force)
SB 6569 was an initiative that passed into law by a veto override vote during a special session that adjourned in March to end the two-year legislative cycle (2015-2016). The bill creates a task force to study the high out-of-pocket costs for patients.
Task force members will be required to study the following issues associated with high out-of-pocket costs:
- Evaluate factors contributing to the high out-of-pocket costs for patients.
- Consider patient treatment adherence and the impacts on chronic illness and acute disease.
- Discuss the impact when patients cannot maintain access to their prescription drugs and the implications of adverse health impacts.
- Consider the impact of the factors on affordability of health care coverage.
Recommendations by the task force are required to be submitted to the appropriate committees by December 2016. WRA’s legislative staff will monitor scheduled task force hearings and provide updates as necessary.
Senate Bill 5935 (Biological Products)
SB 5935 authorizes a biological product to be substituted in the place of another biological product. Before allowing pharmacist to make the switch, they must adhere to the following:
- Prescription must be marked “substitution permitted.”
- The substitute product has to be lower than the wholesale price of the original biologic.
- Pharmacist must notify the prescriber and inform the patient of the substitution.
The bill took effect on July 24, 2015.
Other State News Stories of Interest
M.D. Phone Home: New Legislation Expands Telemedicine in Washington
New law fights “doc-shopping” by addicts
Washington Legislature: What passed, died and was revived
State revokes, suspends licenses, certifications, registrations of health care providers
Medicare Part B Sparks Opposition
Centers for Medicare and Medicaid Services (CMS) recently proposed a new payment structure for Medicare Part B drugs, leaving Rheumatologist and other physicians across the country with serious concerns about access to care for their patients. The new plan looks to reduce the reimbursement of Part B drugs from ASP + 6% to ASP +2.5% and a fixed $16.80 per day. To combat the measure, opponents have been publically engaged as over 300 groups have already sent letters urging House and Senate leadership to advise CMS to rethink their position.
WRA has been tracking the issue on an ongoing basis and will look to provide resources for rheumatologists and their practices to oppose the Part B model. WRA will also be providing comments to CMS during their open comment period which ends on May 9.
FDA Approves Biosimilar to Remicade
The U.S. Food and Drug Administration have approved Inflectra (infliximab-dyyb) for multiple indications. The biosimilar can be prescribed by a health care professional for the treatment of rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, ulcerative colitis and crohn’s disease. This is the second biosimilar to be approved by the FDA.
Other Federal News Stories of Interest
The HIPAA Audits are Coming, The HIPAA Audits are Coming
Report Offers a Mixed View of Health Care Law Costs
CMS finalizes mental health and substance use disorder parity rule for Medicaid and CHIP
FDA Issues Draft Guidance for Labeling Biosimilars