JointHealth™ express August 15, 2014
Call for patient input on subsequent entry biologic infliximab (Remsima™ and Inflectra™) for ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, and/or rheumatoid arthritis
Do you have ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, and/or rheumatoid arthritis or care for someone who does? We need your valuable input.
Health Canada defines subsequent entry biologics (SEBs) as biologic medicines that are similar to, and would enter the market after an approved innovator biologic (such as Remicade®).
Unlike the more common small-molecule drugs, biologics generally exhibit high molecular complexity, and are sensitive to changes in manufacturing practices. SEBs are not identical to their innovator products because their chemical characteristics cannot be precisely duplicated during the manufacturing process. Therefore, SEBs may have unique efficacy, immunogenicity, and safety profiles that are different from their innovator products.
The Common Drug Review (CDR) is currently welcoming patients and their caregivers to provide input on the manufacturer’s submission for infliximab (Remsima™) and infliximab (Inflectra™) for the treatment of ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, and rheumatoid arthritis in adults. The innovator biologic, or reference product, is infliximab (Remicade®). The JointHealth™ Report Card provides the current indications for Remicade®. Both Remsima™ and Inflectra™ are administered intravenously (IV) in the hand or arm.
The CDR is part of the Canadian Agency for Drugs and Technologies in Health (CADTH). The CDR conducts objective, rigorous reviews of the clinical and cost effectiveness of drugs, and provides drug formulary recommendations to the publicly funded drug plans in Canada (except Quebec).
To help them make their recommendations, the CDR accepts input from patient groups, like Arthritis Consumer Experts (ACE). Because patient input is vitally important to government decision-making about medications, we would like to gather your views and share them with the CDR.
These are the questions they are asking:
Please contact us at info@jointhealth.org to provide your input or arrange for a phone interview at 604-974-1366.
Call for patient input on subsequent entry biologic infliximab (Remsima™ and Inflectra™) for ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, and/or rheumatoid arthritis
Do you have ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, and/or rheumatoid arthritis or care for someone who does? We need your valuable input.
Health Canada defines subsequent entry biologics (SEBs) as biologic medicines that are similar to, and would enter the market after an approved innovator biologic (such as Remicade®).
Unlike the more common small-molecule drugs, biologics generally exhibit high molecular complexity, and are sensitive to changes in manufacturing practices. SEBs are not identical to their innovator products because their chemical characteristics cannot be precisely duplicated during the manufacturing process. Therefore, SEBs may have unique efficacy, immunogenicity, and safety profiles that are different from their innovator products.
The Common Drug Review (CDR) is currently welcoming patients and their caregivers to provide input on the manufacturer’s submission for infliximab (Remsima™) and infliximab (Inflectra™) for the treatment of ankylosing spondylitis, plaque psoriasis, psoriatic arthritis, and rheumatoid arthritis in adults. The innovator biologic, or reference product, is infliximab (Remicade®). The JointHealth™ Report Card provides the current indications for Remicade®. Both Remsima™ and Inflectra™ are administered intravenously (IV) in the hand or arm.
The CDR is part of the Canadian Agency for Drugs and Technologies in Health (CADTH). The CDR conducts objective, rigorous reviews of the clinical and cost effectiveness of drugs, and provides drug formulary recommendations to the publicly funded drug plans in Canada (except Quebec).
To help them make their recommendations, the CDR accepts input from patient groups, like Arthritis Consumer Experts (ACE). Because patient input is vitally important to government decision-making about medications, we would like to gather your views and share them with the CDR.
These are the questions they are asking:
- What are the disease-related symptoms and problems that impact the patients' day-to-day life and quality of life? For example: what aspects of their disease are more important to control, how does their disease affect day-to-day life, and are there any activities that the patient is not able to do as a result of their disease?
- How well are patients managing their disease with currently available treatments? Examples of the types of information to be included in the answer are:
- Are patients using or have they ever used the originator (Remicade®) for the treatment of their disease?
- What therapy are patients using for the treatment of their disease?
- How effective are current treatments in controlling the common aspects of the disease?
- Are there needs, experienced by some or many patients, which are not being met by the current treatments? What are these needs?
- Do current treatments have adverse effects that are more difficult to tolerate than others? What are they?
- Do patients have difficulty accessing current treatments because of costs, such as costs related to travel and drug administration costs?
- When offered, how do the patient assistance or support programs impact on the accessibility and effectiveness of the treatment?
- How does the disease affect caregivers?
- What challenges do family and friends who support a patient to manage the disease face?
- What impact does the treatment have on the caregivers’ daily life, such as emotional/psychological effects, fatigue, stress, and physical challenges?
- What are patients’ expectations for the SEB?
- What are the perceived advantages or disadvantages of the SEB?
- What are the aspects of the patients’ disease that it is hoped will be addressed?
Please contact us at info@jointhealth.org to provide your input or arrange for a phone interview at 604-974-1366.
Arthritis Consumer Experts
ACE thanks Arthritis Research Canada (ARC) for its scientific review of ACE and JointHealth™ information and education programs.