The Canadian Agency for Drugs and Technologies in Health (CADTH) is an independent, not for profit agency that is funded by Canada’s federal, provincial, and territorial governments, and which provides evidence-based information to health care leaders and policy makers about the effectiveness and efficiency of health technologies (i.e. drugs and medical devices). All new drugs and medical devices that are approved in Canada undergo a CADTH review, which is a process that also calls for input from patient groups. In the case of drugs, this is called the Common Drug Review or CDR. CAPA believes it is important to provide CDR input on all arthritis-related drugs so that there are many options available for people who live with arthritis. When CAPA undertakes submissions to CADTH’s CDR, it tries to ensure that voices and experiences of those patients who have used the drug under review are heard.
To learn more about the process of the CADTH CDR, including all stakeholders who provide input to CADTH, please refer to the process documenton CADTH’s website here.
CAPA developed and presented a poster presentation for the 2015 CADTH Symposium. The poster highlighted our involvement in providing patient evidence submissions to the CDR process.
CAPA posts its CADTH submissions below, and if you would like your voice heard in the patient input submission process, please visit CAPA’s Facebook page for more information on how to contribute to current submissions that are underway.
Note that Ontario and Quebec also have a patient input submission process to which CAPA also provides input – and our submissions to those calls are below the CADTH submissions.
Submissions to CADTH
Click on the titles below to see the submissions CAPA has prepared and submitted to CADTH.
- Upadacitinib for the treatment of psoriatic arthritis (PsA) (CAPA and the Arthritis Society submission)
- Anakinra (Kineret) for Still’s disease and SJIA in adults and pediatric patients (CAPA, the Arthritis Society and Cassie & Friends submission)
- Ixekizumab for ankylosing spondylitis (joint CAPA & TAS submission)
- Upadacitinib for rheumatoid arthritis (joint CAPA & TAS submission)
- Benlysta (belimumab) for systemic lupus erythematosus (SLE) (joint CAPA & TAS submission)
- Input on CADTH’s patient input template for subsequent entry biologics
- Input on conventional synthetic disease-modifying anti-rheumatic drugs (csDMARD’s)
- Input on availability and access to non-pharmacological treatments for chronic non-cancer pain
- Actemra (Tocilizumab) subcutaneous for Rheumatoid Arthritis
- Baricitinib for Rheumatoid Arthritis
- Canakinumab for Systemic Juvenile Idopathic Arthritis (SJIA)
- Cosentyx (Secukinumab) for Ankylosing Spondylitis
- Cosentyx (Secukinumab) for Psoriatic Arthritis
- Cimzia for Ankylosing Spondylitis
- Inflectra (Infliximab) for Ankylosing Spondylitis
- Inflectra (Infliximab) for Psoriatic Arthritis
- Inflectra (Infliximab) for Rheumatoid Arthritis
- Ixekizumab for Psoriatic Arthritis
- Nucynta for treatment of pain
- TBC (Etanercept) for Ankylosing Spondylitis
- TBC (Etanercept) for Rheumatoid Arthritis
- Remsima (Infliximab) for Ankylosing Spondylitis
- Remsima (Infliximab) for Psoriatic Arthritis
- Remsima (Infliximab) for Rheumatoid Arthritis
- Sarilumab for Rheumatoid Arthritis
- Xeljanz (Tofacitinib) for Rheumatoid Arthritis
Submissions to Ontario, Quebec and BC
- OPDP Actemra (self-injectable) for Rheumatoid Arthritis
- OPDP Apremilast (Otezla) for Psoriatic Arthritis
- OPDP Cimzia for Psoriatic Arthritis
- OPDP Cimzia for Ankylosing Spondylitis
- OPDP Inflectra (Infliximab) for Ankylosing Spondylitis
- OPDP Inflectra (Infliximab) for Psoriatic Arthritis
- OPDP Inflectra (Infliximab) for Rheumatoid Arthritis
Note that CAPA has provided submissions to BC Pharmacare through their online program for:
- Cimzia – Psoriatic Arthritis and Ankylosing Spondylitis
- Cosentyx – Ankylosing Spondylitis
- Xeljanz – Rheumatoid Arthritis