MORQUIO IN CANADA

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AN ONLINE RESOURCE FOR MORQUIO A SYNDROME PATIENTS AND THEIR FAMILIES
What is Morquio A Syndrome?
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What is Morquio A Syndrome?

Morquio A Syndrome is a rare and debilitating genetic disorder. It is a form of Mucopolysaccharidosis (MPS IVA) and is characterized by significant bone and joint disease, as well as numerous other symptoms throughout the body.

Patients suffering from Morquio A Syndrome lack an enzyme in their blood that breaks down cellular waste in the body. This waste builds up and stores in the bones, tissues, organs, and muscles, and leads to some of the symptoms described below.

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MORQUIO QUICK STATS

100

Estimated Morquio A Syndrome Cases in Canada

21

Canadian Clinical Trial Participants

32

Weeks Since Life-Sustaining ERT (VIMIZIM) Treatment Approved by Health Canada

1

Patients Receiving Reimbursed Treatment in Canada  

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What Causes Morquio A Syndrome?

Morquio A Syndrome is an inherited genetic disorder caused by a deficiency of an enzyme called N-acetylgalactosamine-6 sulfatase, or GALNS. Deficiency of this enzyme causes cellular waste to build up in the body and progressively store in the bones, tissues, organs, and muscles. Morquio A Syndrome is estimated to occur in 1 in 200,00 to 300,000 live births, with 90-100 estimated cases in Canada.

Genetic Condition Caused By Enzyme Deficiency

Missing or deficient enzyme (GALNS) causes cellular waste from the cells to store in the bones, tissues, organs, and muscles.  This disease is characterized as a lysosomal storage disorder.

Lysosomal Storage Leads To Progressive Symptoms

Virtually all bones, muscles, organs, and tissues in the body are affected by GALNS deficiency, leading to progressive, multi-systemic and debilitating symptoms.

First Ever Treatment Now Available

The FDA, the European Commission, and Health Canada have all approved the first ever treatment for Morquio A Syndrome.  Developed by Biomarin Pharmaceuticals, this enzyme replacement therapy (ERT) delivers a synthetic version of the GALNS enzyme into the bloodstream.

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Symptoms of Morquio A

There are many symptoms and associated consequences for patients suffering from Morquio A Syndrome. Until recently, management of symptoms was the only course of care for patients. In 2014, the first ever treatment for Morquio A was approved by the FDA, the European Commission, and Health Canada. More information on this new treatment can be found in our TREATMENT section.

Heart and Airway Disease

People suffering from Morquio A Syndrome can develop respiratory failure, severe sleep apnea, and upper airway collapse.  Affected individuals may also develop numerous and recurrent respiratory infections and a thickening of the heart valves.

Skeletal Symptoms

People with Morquio A Syndrome may have a wide range of skeletal symptoms.  These can include shortened stature, spinal cord compression, bone deformities, chest protrusion, kyphosis, and scoliosis.

Hearing Loss

Usually common in the second decade of life, hearing loss can be progressive and severe.

Eye and Vision Issues

Some people with Morquio A Syndrome may develop severe corneal clouding and a debilitating decease in vision.

Frequent Hospital Visits

People with Morquio A Syndrome have frequent hospital stays for surgical procedures and to manage the symptoms of the disease.

Specialist Care

Patients battling Morquio A Syndrome often visit numerous specialists to help manage their disease.  These can include, but aren’t limited to, MPS Genetics Specialists, Neurologists, Ophthalmologists, Orthopaedic Specialists, Cardiologists, ENTs, Pulmonologists,  and Rheumatologists.  

Surgical Interventions

In almost all cases of Morquio A Syndrome, patients need multiple surgical procedures.  These may include skeletal corrections, corneal transplants, heart valve replacements, spinal cord decompression, and other procedures.

Decreased Endurance

Studies have shown that endurance of affected individuals is impacted greatly due to the progression of the disease.  Endurance has an impact on all facets of life.  Recent clinical trials have shown a significant increase in endurance for all patients receiving enzyme replacement therapy.

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Treatment with Vimizim for Morquio A

New Hope for Morquio A Patients and Their Families

In 2014, the first ever treatment for Morquio A Syndrome was approved in the US, European Union, and Canada.  Vimizim, created by Biomarin Pharmaceuticals, is a synthetic version of the GALNS enzyme that patients are lacking in their blood.  This enzyme replacement therapy (ERT) was fast-tracked through the approval process in both the US and Canada because of the tremendous unmet need the treatment provided patients.

Clinical trial results were very promising, with patients seeing a sizeable increase in endurance, an excellent indicator for how well the treatment works.  Endurance measures how well a patient’s body is performing.  From heart to bones to pulmonary function, increased endurance indicates that those systems are working better.

Jump To Biomarin’s Vimizim Information Page
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" This has given our family the chance to think a little further into the boys’ future and to dream again of all the things they will be able to do and accomplish. It’s given us back the hope that was taken from us so long ago when we were diagnosed! "
Debbie Braun – Mother of 2 children with Morquio A Syndrome - Ontario, Canada

 

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Access to Treatment in Canada

 Reimbursement for Rare Diseases in Canada – A Long and Arduous Process

From an access standpoint, there is no reason for delay, and no reason why patients who need access can’t receive it soon after regulatory approval from Health Canada.  Patients suffering from these rare and progressive diseases don’t have the luxury of time on their side, and the current process is long and arduous. Andrew McFadyen, Executive Director, The Isaac Foundation

Unfortunately, any approval by Health Canada for treatments for a Rare Disease doesn’t mean that patients can begin receiving therapy immediately.  Canada’s lack of an Orphan Drug Plan, coupled with a very illogical approval process that differs in individual provinces, often leaves patients lacking the treatment they desperately need.  The reason?  While Health Canada may approve a treatment for use, it’s still up to individual provinces to decide whether they will pay for the treatment or not.  This leaves Canadians with inequitable access to our health care system, with some patients receiving treatment for their conditions based solely on what part of the country they happen to live in.

Physicians with patients suffering from a rare disease need to fill out a request for reimbursement application and submit it to the provincial Ministry of Health.  From there, the application is reviewed and a decision to cover the cost of treatment is either approved or, in most cases, denied.  Most reasons governments provide for denial are due to a lack of evidence of the benefits these treatments provide patients, even when significant data exists to show such benefits exist.  The true reason these therapies are denied is cost – provinces feel the cost to treat individuals is a burden on their health care budgets.

More often than not, patients and their families are forced to advocate and lobby provincial governments to cover the cost of the treatments they need.  Grassroots social media campaigns, press releases, and demonstrations are all common mechanisms that people use during their lobbying efforts.  Sometimes they are successful, oftentimes they are not, and many patients needing therapy go untreated.  In Canada, organizations like The Isaac Foundation and RQMO work with families and governments to help ensure patients needing treatment for rare diseases gain access in a timely and equitable manner.

Beaurocratic Path to Reimbursement – Information and Estimated Timelines 

7

Months to Review and Receive Approval from Health Canada (Approval: July, 2014)

8

Months Estimated to Complete COMMON DRUG REVIEW process (Application Submitted: August, 2014)

12

Months Estimated to Negotiate Reimbursement Cost through the Pan-Canadian Pricing Alliance (Submission after CDR is completed)

Beaurocratic Path to Reimbursement Could Take 20 Months or More 

Health Canada Approval Announcement

Common Drug Review Information and Website

 

Pan-Canadian Pricing Alliance Website

 

STEP 1 - Approval By Health Canada

Biomarin submits VIMIZIM to Health Canada for review and approval for use in Canada.  The review was considered a “priority” review because of the potential impact the therapy could have on patients.  Submission took place in December of 2013, and approved by Health Canada in July of 2014.

STEP 2 - Submission and Review to the Common Drug Review (CDR)

The Common Drug Review  is a “process for conducting objective, rigorous reviews of the clinical, cost-effectiveness, and patient evidence for drugs.”  The CDR completes their review and recommends to provinces whether a drug should be reimbursed or not.

STEP 3 - Negotiations Begin With the Pan-Canadian Pricing Alliance (PCAP)

The Pan-Canadian Pricing Alliance works to capitalize “on the combined ‘buying power’ of drug plans across multiple provinces and territories” to bring the cost of expensive treatments down.  

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Support for Accessing Treatment in Canada

If you would like assistance obtaining VIMIZIM treatment in Canada, please don’t hesitate to contact us and we will do whatever we can to assist.

We can join you for a meeting with your Member of the Provincial Parliament (MPP) or  Member of the Legislature (MLA) and work closely with them to ensure reimbursement for treatment is forthcoming.  We can also help you connect with other families undertaking the same processes, connect with the drug company that makes VIMIZIM (Biomarin Pharmaceuticals) on your behalf, and come meet with you in your home province to help support you in any way necessary.

Whatever we can do to help, we’ll be here.

If you would rather connect with us via social media, please find us on the links below:

 

Morquio in Canada

 

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Latest From The Blog…

We'll do our best to update our blog as often as possible. Please check back often for our latest entries!

Saskatoon family awaits answer on treatment for crippling disease

Three children all suffer from genetic enzyme deficiency that could lead to early death CBC News Posted: Sep 15, 2015 5:30 AM CT Last Updated: Sep 15, 2015 6:43 AM CT A family in Saskatoon is waiting and hoping for the solution to a triple heartbreak. Three of the five children suffer from a crippling genetic disease that could kill

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FOR IMMEDIATE RELEASE – SASKATOON SIBLINGS AWAIT FUNDING FOR LIFE-SAVING TREATMENT

Children Diagnosed With Ultra-Rare Condition; Treatment Already Being Funded In Ontario and Quebec (Sept. 14, 2015) The Saskatchewan Ministry of Health is currently considering an application for exceptional funding of a life-sustaining treatment required by three siblings from Saskatoon. 8 year-old Sara Amir, along with her siblings Khadija, 10 and Muhammad, 12 have been diagnosed with Morquio Syndrome, and all

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  • @CarlWMayer Ha. This made me laugh more than I expected. Nicely done…
    Andrew McFadyen about 12 hours ago
  • RT @ArthurCaplan: Comparison of Wait Times for New Patients Between the Private Sector and VA Medical Centers https://t.co/N0JLfrutdg. VA…
    Andrew McFadyen about 1 days ago
  • RT @sarah_harmer: Reminder to spend a few minutes this wknd standing up for our living systems & wise longterm planning. Don't sit this one…
    Andrew McFadyen about 1 days ago
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Canadian Morquio A News

Families and advocacy groups through the country are doing an incredible job raising awareness of Morquio A Syndrome. We'll post newspaper reports, television, and radio appearances here as quickly as they come in. If you have a news item to share, please send it along for inclusion on this page!

CTV NEWS SASKATOON – PROVINCE ASKED TO FUND TREATMENT
New therapy helps London teen with ‘ultra-rare’ disorder
Drug brings hope for teen battling rare disorder
A London boy’s fight with rare disease
Hold on to your dreams – Adult living with Morquio meets Cornwall-area child
RQMO applauds Health Canada’s approval of first treatment for Morquio A syndrome
Barb Larson on AM630 CHED’s “Tencer and Grose”
Health Canada Approves Vimizim to Treat Rare Disease
Morquio Family Tree fundraising for rare disease
CTV NEWS SASKATOON – PROVINCE ASKED TO FUND TREATMENT

CTV NEWS SASKATOON – PROVINCE ASKED TO FUND TREATMENT

Television
New therapy helps London teen with ‘ultra-rare’ disorder

New therapy helps London teen with ‘ultra-rare’ disorder

Web/Mobile
Drug brings hope for teen battling rare disorder

Drug brings hope for teen battling rare disorder

Television, Web/Mobile
A London boy’s fight with rare disease

A London boy’s fight with rare disease

Newspaper, Web/Mobile
Hold on to your dreams – Adult living with Morquio meets Cornwall-area child

Hold on to your dreams – Adult living with Morquio meets Cornwall-area child

Newspaper, Web/Mobile
RQMO applauds Health Canada’s approval of first treatment for Morquio A syndrome

RQMO applauds Health Canada’s approval of first treatment for Morquio A syndrome

Web/Mobile
Barb Larson on AM630 CHED’s “Tencer and Grose”

Barb Larson on AM630 CHED’s “Tencer and Grose”

Radio
Health Canada Approves Vimizim to Treat Rare Disease

Health Canada Approves Vimizim to Treat Rare Disease

Newspaper, Web/Mobile
Morquio Family Tree fundraising for rare disease

Morquio Family Tree fundraising for rare disease

Newspaper, Web/Mobile

CONTACT US AND SHARE YOUR STORY!

We want to hear from you! Send us your story so we can share it with the world. Every person and family battling Morquio A Syndrome has a unique story to tell - one of bravery, resilience, and perseverance. We'll share all stories online here and on our social media feeds!