tara

tara
LA Mayor's Office Acknowledges the NDF's Advocacy with GNEM

Thursday, February 27, 2014

National Institutes of Health to Host a Series of Events to Address Rare Disease Day



The NIH will be celebrating Rare Disease Day on February 28th.  There are over 6500 rare diseases.  The event is free to the public and is held at the NIH in Bethesda, Maryland.  I have attached the link.
https://events-support.com/Documents/AGENDA_RDD14.pdf



Wednesday, February 26, 2014

A Conglomeration of List of Links and Updates On HIBM (GNE Myopathy)

It appears that rare diseases are getting more coverage in the media and bio-pharmaceutical companies are willing to take on the tasks of research and drug trials
.http://www.phrma.org/working-together-we-can-produce-results

1.  Ultragenyx, the company that is conducting the Sialic Acid (extended and immediate release) tablets for HIBM has started trading their stock on Wall Street now.  They use the ticker symbol RARE.  Here is a link on their presentation and an upcoming event.  On March 5th they will be having a  Health care conference of which it seems one could register for.
  http://ir.ultragenyx.com/events.cfm

2.  The LA Marathon will be happening on March 9th. and there is a site set up for those who would like to participate or donate. http://www.crowdrise.com/runforhibm2014/fundraiser/sandradarvish

3. Ultragenyx is recruiting participants for a Combined Registry Prospective Natural History Study.  They are recruiting participants in the United Kingdom, Canada, and the United States.  I see also listed are France and Bulgaria  however they are not recruiting yet.  Here is the link:
http://clinicaltrials.gov/ct2/show/NCT01784679?term=hibm&rank=2

4.  The National Institutes of Health still seems to be recruiting for their natural history study:
http://clinicaltrials.gov/ct2/show/NCT01417533?term=hibm&rank=4

5.  There is support group on  facebook for patients and family with HIBM.  This is a very helpful group of people who offer tips on how to manage our disease.  We also started a Google hangout group and this was quite informative to see and chat with others.

Please feel free to contact me if you need more information in this blog.
Thank you for visiting this blog.

Monday, January 6, 2014

Affordable Testing for HIBM Will Take Place in Los Angeles, California on January 12th. 2014


For those who  are living in Los Angeles, California  or can make there this weekend,  please use this opportunity to get tested for HIBM.
NDF is proud to partner with Sinai Temple and the Los Angeles Jewish Genetic Disease Project to finally bring affordable genetic disease screening to Los Angeles. Together we can stop HIBM from passing to the next generation.
Please refer to this link.

https://www.facebook.com/events/397791307033701/

Saturday, December 28, 2013

End of 2013 With Promising Developments in Research and Trials of HIBM/GNE Myopathy

Dear friends, family and readers:
I wish you a joyful conclusion to 2013 and  may 2014 bring you joy, good tidings, and peace. I continue to forge ahead  with my participation in a clinical trial for HIBM.
There has been some progress with the clinical trials conducted by NIH and Ultragenyx Pharmaceutical.  NIH concluded the phase 1 trial with ManNac and will be starting phase 2 in the near future.  Ultragenyx Pharmaceutical has concluded extended phase 2 with the Sialic Acid Extended Release SA-ER tablets and has started patients on Sialic Acid Immediate Release (SA-IR) in addition to the SA-ER tablets.  The total dose per day is 12,000 mg. In addition to the 46 patients who were in the trial already, they are recruiting 10 new patients -"treatment naïve subjects" (those who have never taken sialic acid)  for this current trial.  Here is the link with the details.

http://clinicaltrials.gov/ct2/show/NCT01830972?term=hibm&rank=5


Ultragenyx Pharmaceutical  found the following based on preliminary data in phase 2 trial which is quite promising.
"Similar to the results observed at the 24-week interim analysis, at 48 weeks the
comparison of the upper extremity composite of muscle strength for the combined
group of patients on 6 grams showed a modest increase and a statistically significant
difference relative to the decline in strength observed in the combined groups on 3
grams. In the 6-gram cohort treated for 48 weeks, the modest increase in upper 
extremity strength observed at 24 weeks was sustained relative to a further decline in 
the comparable 3-gram group. These changes were more pronounced in those patients
that have less advanced disease as assessed by a greater walking ability at baseline, a
predefined subset. The lower extremity composite did not show a statistically significant
difference between the dose groups, but neither group showed a significant decline
during the treatment period."

These 48 week data suggest that 6 grams per day of SA-ER is mitigating the normally 
expected decline in upper extremity muscle strength,” said Emil Kakkis, M.D., Ph.D.,
Chief Executive Officer of Ultragenyx. “The maintenance of this effect from the 24-week
data is encouraging. Given the difference between the dose groups and good safety
profile, we plan to test an even higher dose of sialic acid in these patients who have no
other approved treatment options.”
I have attached the link of their complete press release here.
http://www.ultragenyx.com/index.php?ht=a/GetDocumentAction/i/17531


The acronym HIBM (Hereditary Inclusion Body Myopathy) has been widely used to describe the muscle wasting disease and  also has been confused with another disease, therefore the name of HIBM is now changed to GNE myopathy which more accurately defines this disease as it is on this gene - GNE where the deficiency happens. I will gradually change my blog name to "Tara Talks GNE Myopathy". Here is some discussion on this topic.

"There is confusion in some circumstances with the very similar names of two quite different medical disorders; Inclusion Body Myositis and Hereditary Inclusion Body Myopathy. This press release is to advise that Inclusion Body Myositis is NOT THE SAME as HIBM (myopathy). Because of this confusion, NZP supports the name change of Hereditary Inclusion Body Myopathy (HIBM) to “GNE myopathy” (see; http://dx.doi.org/10.1016/j.ymgme.2012.10.011).
Myositis is a mostly inflammatory muscle disease and mostly occurring sporadically in elderly people. There is no inflammation in HIBM/GNE myopathy and GNE myopathy has a much earlier onset than myositis. Also HIBM/GNE myopathy is a genetic disease, while for Inclusion Body Myositis no common genetic component has been identified.
 
To make the names more confusing, inclusion body myositis is abbreviated as sIBM (sporadic inclusion body myositis). More about sIBM can be found at: http://omim.org/entry/147421.
In some publications, Inclusion Body Myositis is called IBM1 and HIBM/GNE myopathy is called IBM2."

http://www.nzp.co.nz/index.php/news/7-news/79-ibm-hibm-and-gne-myopathy.html

"GNE myopathy, previously termed hereditary inclusion body myopathy (HIBM), is an adult-onset neuromuscular disorder characterized by progressive muscle weakness. The disorder results from biallelic mutations in GNE, encoding UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, the key enzyme of sialic acid synthesis. GNE myopathy, associated with impaired glycan sialylation, has no approved therapy. "

http://www.sciencedirect.com/science/article/pii/S1096719212003794


Best wishes for 2014.





Saturday, November 16, 2013

A Profoundly Touching Video of a Friend with HIBM

This is quite a moving video of a friend who also has HIBM.  She gave this speech at the annual fundraising gala event for the Neuromuscular Disease Foundation.  http://www.ndf-hibm.org/

The video is about thirteen minutes long.  In her speech Jennifer poignantly describes what it is like to inhabit  a body that suffers from HIBM. She has effectively encapsulate  the whole spectrum of feelings of HIBM patients and their daily challenges.

Please take the time to watch this video, and visit the NDF web site.
Thank you Jennifer. 
http://vimeo.com/79357093

Sunday, November 3, 2013

A More Functional Sleek Designed Wheel Chair With Reviews From Gizmodo


Finally, a wheel chair is coming on the market with functionality and "good looks" for people with disabilities.  I feel this company has done it's research in how people could more effectively use a wheel chair that assists in maintaining proper posture, ease in getting up, and sitting down. I had the pleasure of meeting one of it's founder and I am impressed with their vision to create this chair. Check out the wheel technology and the turning radius.  I do not know the cost for such a chair yet and if and when Medicare will cover it.  Please feel free to contact the company.
Best wishes to all my readers.  May your light continue to shine.
Tara

http://whill.jp/


Type-A is classified as a non-medical device. So, people will need to buy WHILL Type-A out of pocket... We plan to receive FDA clearance with our future model and already got started with it.


Review of this chair by Gizmodo
http://gizmodo.com/this-professor-x-approved-futuristic-wheelchair-is-arri-1450704347

Friday, October 11, 2013

Friend from Japan with HIBM/gne Myopathy, Japanese Registry, and Recent Research on HIBM

 I recently had the pleasure of meeting a friend from Japan who like me has HIBM. Yuriko travelled to the United States to visit  the National Institutes of Health in Bethedsa, Maryland and attend a HIBM symposium held in San Francisco, California. Yuriko started noticing weakness associated with HIBM in her early twenties and is the only one in her family affected.  She currently uses  a wheel chair and is getting weaker as this disease progresses.  She is the vice president for  the Patients Association for Distal Myopathies or PADM in Japan. This is a patient organization which is very active in pursuing a treatment for HIBM.  There are over 130 members in this  association which is quite a high number for a rare disease. There are two well known researchers of HIBM  (Dr. I. Nishino and Dr. I. Nonaka)  on their Academic Advisory board.

It was very insightful to meet Yuriko and her husband.  I find Yuriko  brave to travel such a long distance, as in my experience  with my disability a flight of only five hours is my limit.  There are many barriers at the airports, getting on and off  the plane for one to overcome when using a wheelchair.  It was  quite insightful for me to meet another patient with HIBM and observe how gracefully Yuriko is able to manage her disability.





Link for the PADM association.
http://enigata.com/index_e.html

There is a Japanese GNE myopathy registry which was set up in 2012. 
 http://www.remudy.jp/dmrv/index.html

A research abstract recently published on Japanese patients.
I find this  information quite interesting from this abstract that there were able to profile 212 patients as with rare diseases it is quite difficult to get that many patients.. "Here, we report the mutation profile of the GNE gene in 212 Japanese GNE myopathy patients, which is the largest single-ethnic cohort for this ultra-orphan disease. We confirmed the clinical difference between mutation groups. However, we should note that the statistical summary cannot predict clinical course of every patient."
http://europepmc.org/abstract/MED/24027297

Just a personal note to my friends from far and near,  I continue to participate in a clinical trial in the U.S and I am well.

Thursday, August 1, 2013

Conglomeration of Articles, Updates, and Announcements


This is an article from the New York Times discussing the effects of exercise on muscles. Since our muscles deteriorate with HIBM, I think this is a well written article which discusses "epigenetics" and muscles.  It also lists the research being done in this area.

Exercise promotes health, reducing most people’s risks of developing diabetes and growing obese. But just how, at a cellular level, exercise performs this beneficial magic — what physiological steps are involved and in what order — remains mysterious to a surprising degree.
Several striking new studies, however, provide some clarity by showing that exercise seems able to drastically alter how genes operate.
Genes are, of course, not static. They turn on or off, depending on what biochemical signals they receive from elsewhere in the body. When they are turned on, genes express various proteins that, in turn, prompt a range of physiological actions in the body.
One powerful means of affecting gene activity involves a process called methylation, in which methyl groups, a cluster of carbon and hydrogen atoms, attach to the outside of a gene and make it easier or harder for that gene to receive and respond to messages from the body. In this way, the behavior of the gene is changed, but not the fundamental structure of the gene itself. Remarkably, these methylation patterns can be passed on to offspring – a phenomenon known as epigenetics.
What is particularly fascinating about the methylation process is that it seems to be driven largely by how you live your life. Many recent studies have found that diet, for instance, notably affects the methylation of genes, and scientists working in this area suspect that differing genetic methylation patterns resulting from differing diets may partly determine whether someone develops diabetes and other metabolic diseases.
But the role of physical activity in gene methylation has been poorly understood, even though exercise, like diet, greatly changes the body. So several groups of scientists recently set out to determine what working out does to the exterior of our genes.
The answer, their recently published results show, is plenty.
Of the new studies, perhaps the most tantalizing, conducted principally by researchers affiliated with the Lund University Diabetes Centre in Sweden and published last month in PLoS One, began by recruiting several dozen sedentary but generally healthy adult Swedish men and sucking out some of their fat cells. Using recently developed molecular techniques, the researchers mapped the existing methylation patterns on the DNA within those cells. They also measured the men’s body composition, aerobic capacity, waist circumference, blood pressure, cholesterol levels and similar markers of health and fitness.
Then they asked the men to start working out. Under the guidance of a trainer, the volunteers began attending hourlong spinning or aerobics classes approximately twice a week for six months. By the end of that time, the men had shed fat and inches around their waists, increased their endurance and improved their blood pressure and cholesterol profiles.
Less obviously, but perhaps even more consequentially, they also had altered the methylation pattern of many of the genes in their fat cells. In fact, more than 17,900 individual locations on 7,663 separate genes in the fat cells now displayed changed methylation patterns. In most cases, the genes had become more methylated, but some had fewer methyl groups attached. Both situations affect how those genes express proteins.
The genes showing the greatest change in methylation also tended to be those that had been previously identified as playing some role in fat storage and the risk for developing diabetes or obesity.
“Our data suggest that exercise may affect the risk for Type 2 diabetes and obesity by changing DNA methylation of those genes,” says Charlotte Ling, an associate professor at Lund University and senior author of the study.
Meanwhile, other studies have found that exercise has an equally profound effect on DNA methylation within human muscle cells, even after a single workout.
To reach that conclusion, scientists from the Karolinska Institute in Stockholm and other institutions took muscle biopsies from a group of sedentary men and women and mapped their muscle cell’s methylation patterns. They then had the volunteers ride stationary bicycles until they had burned about 400 calories. Some rode strenuously, others more easily.
Afterward, a second muscle biopsy showed that DNA methylation patterns in the muscle cells were already changing after that lone workout, with some genes gaining methyl groups and some losing them. Several of the genes most altered, as in the fat cell study, are known to produce proteins that affect the body’s metabolism, including the risk for diabetes and obesity.
Interestingly, the muscle cell methylation changes were far more pronounced among the volunteers who had ridden vigorously than in those who had pedaled more gently, even though their total energy output was the same.
The overarching implication of the study’s findings, says Juleen Zierath, a professor of integrative physiology at the Karolinska Institute and senior author of the study, is that DNA methylation changes are probably “one of the earliest adaptations to exercise” and drive the bodily changes that follow.
Of course, the intricacies of that bogglingly complex process have yet to be fully teased out. Scientists do not know, for instance, whether exercise-induced methylation changes linger if someone becomes sedentary, or if resistance training has similar effects on the behavior of genes. Nor is it known whether these changes might be passed on from one generation to the next. But already it is clear, Dr. Ling says, that these new findings “are additional proof of the robust effect exercise can have on the human body, even at the level of our DNA.”   http://well.blogs.nytimes.com/2013/07/31/how-exercise-changes-fat-and-muscle-cells/?smid=fb-share&_r=0

The registry for HIBM being conducted by Ultragenyx has added a new site in addition to the British and Canadian sites, they added a U.S. site (although not recruiting). I attended a webinar yesterday on the "Registry" process of rare diseases.  I learned  from the presenters that we as patients need to be included in the design of the "natural history", questionnaires and testing procedures. Please refer to this link:  http://clinicaltrials.gov/ct2/show/NCT01784679?term=hibm&rank=2

To those who are interested in knowing what the doctors and researchers are  finding out about muscles, there will be a World Muscle Society "congress"  to be held from October 1-5th.


 Here is the link to the announcement:   http://www.worldmusclesociety.org/news/read/105

Saturday, July 6, 2013

Phase 2 of the Extension Clinical Trial of Sialic Acid - Extended Release Tablet Recruiting Participants

For those who are interested Ultragenyx has now  opened the extension of Phase 2 study or SA-ER. Seems like you have had to participate in Phase 2 to qualify for this study.  For those interested, please contact the  sites listed.

An Open Label Phase 2 Extension Study of(SA-ER)Tablet

This study is currently recruiting participants.
Verified July 2013 by Ultragenyx Pharmaceutical Inc
Sponsor:
Information provided by (Responsible Party):
Ultragenyx Pharmaceutical Inc
ClinicalTrials.gov Identifier:
NCT01830972
First received: April 10, 2013
Last updated: July 3, 2013
Last verified: July 2013
  Purpose
GNE myopathy or hereditary inclusion body myopathy (HIBM) is a severe progressive metabolic myopathy caused by a defect in the biosynthetic pathway for sialic acid(SA). The purpose of the study is to measure long term safety and the effects of Sialic Acid-Extended Release (SA-ER) pills.


Condition Intervention Phase
GNE Myopathy
HIBM
Drug: SA-ER tabletsPhase 2

Study Type:Interventional
Study Design:Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title:An Open-label Phase 2 Extension Study to Evaluate the Long Term Safety and Efficacy of Sialic Acid-Extended Release (SA-ER) Tablets in Patients With GNE Myopathy or Hereditary Inclusion Body Myopathy


Further study details as provided by Ultragenyx Pharmaceutical Inc:


Primary Outcome Measures:
  • Assess long-term safety of 6000 mg/day SA-ER in HIBM subjects [ Time Frame: approximately 3 years ] [ Designated as safety issue: Yes ]

Estimated Enrollment:45
Study Start Date:June 2013
Estimated Primary Completion Date:June 2016 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
Experimental: open label, 6000 mg/day Drug: SA-ER tablets

Detailed Description:
GNE myopathy or hereditary inclusion body myopathy (HIBM) is a severe progressive metabolic myopathy caused by a defect in the biosynthetic pathway for sialic acid (SA). Substrate replacement therapy is a potential therapeutic strategy based on the success of replacing missing SA and reducing muscle disease in a relevant mouse model of the human disease (Malicdan et al., 2009). Successful use of SA replacement therapy in humans is believed to depend upon providing steady long-term exposure to the compound in an extended release form (such as Sialic Acid-Extended Release [SA-ER]), given SA's short half-life. Following a Phase 1 study to establish the pharmacokinetics for SA-ER and an ongoing Phase 2 study to assess the pharmacodynamic effect of restoring sialylation of muscle by treatment over 48 weeks, Ultragenyx is conducting this study to evaluate the long term safety and efficacy of SA-ER treatment for up to 36 additional months.
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria
Inclusion Criteria:
  • Enrollment in and successful completion of the UX001-CL201 protocol. Must be willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures.
  • Must be willing and able to comply with all study procedures
  • Sexually active subjects must be willing to use an acceptable method of contraception while participating in the study.
  • Females of childbearing potential must have a negative pregnancy test at Baseline and be willing to have additional pregnancy tests during the study.
  • Females considered not of childbearing potential include those who have been in menopause for at least two years, or have had tubal ligation at least one year prior to Baseline, or who have had total hysterectomy.
Exclusion Criteria:
  • Pregnant or breastfeeding at Baseline or planning to become pregnant (self or partner) at any time during the study
  • Use of any investigational product (other than SA-ER tablets) to treat HIBM
  • Ingestion of ManNAc or similar SA producing compounds
  • Has had any hypersensitivity to SA or its excipients that, in the judgment of the investigator, places the subject at increased risk for adverse effects
  • Have any co-morbid conditions, including unstable major organ-system disease(s) that in the opinion of the Investigator, places the subject at increased risk of complications, interferes with study participation or compliance, or confounds study objectives.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01830972


Locations
United States, California
UCLA Medical CenterRecruiting
Los Angeles, California, United States
Contact: Perry Shieh, MD     310-994-5142     pshieh@mednet.ucla.edu    
Principal Investigator: Perry Shieh, MD            
United States, New York
NYU Medical CenterRecruiting
New York, New York, United States, 10016
Contact: Heather Lau, MD     212-263-8344     Heather.Lau@nyumc.org    
Contact: Pankaj Patel     212-263-0139     pankaj.patel@nyumc.org    
Principal Investigator: Heather Lau, MD            
Israel
Hadassah Univeristy HospitalRecruiting
Jerusalem, Israel
Contact: Yoseph Caraco, MD     972-2-6778584     caraco@hadassah.org.il    
Principal Investigator: Yoseph Caraco, MD            

Sponsors and Collaborators
Ultragenyx Pharmaceutical Inc

  More Information

No publications provided

Responsible Party:Ultragenyx Pharmaceutical Inc
ClinicalTrials.gov Identifier:NCT01830972     History of Changes
Other Study ID Numbers:UX001-CL202
Study First Received:April 10, 2013
Last Updated:July 3, 2013
Health Authority:United States: Food and Drug Administration

ClinicalTrials.gov processed this record on July 04, 2013
http://clinicaltrials.gov/ct2/show/NCT01830972?term=hibm&rank=5

Wednesday, July 3, 2013

Breaking News from Ultragenyx; the Company Conducting the Sailic Acid Trial for HIBM

Ultragenyx released their  preliminary findings for the Sialic Acid Extended Release tablet for phase 2 clinical trial.  I have been participating in this study and have just finished my one year on this medicine. I have my personal anecdotal findings , however here is what Ultragenyx have found and it is very encouraging to see that this medicine is showing some hope and improvement in muscle strength.  It is  stated in their News Release:  

"The data showed dose-dependent improvement in muscle strength relative to placebo in some muscle groups, particularly in the upper extremities at the 6-gram dose. These changes were statistically significant or trended towards significance, and were more pronounced in those patients that had greater walking ability at baseline, a predefined subset."

Here is a copy of their complete release.


Transforming good science into great medicine for rare genetic diseases
www.ultragenyx.com
Contact Ultragenyx Pharmaceutical Inc.
For Investor inquiries, Shalini Sharp, Chief Financial Officer
415-483-8800
ssharp@ultragenyx.com
For Media inquiries, Susan Kinkead of Kinkead Communications
415-751-3611
skinkead@kinkeadcomm.com
FOR IMMEDIATE RELEASE:
Ultragenyx Announces a Positive Signal in Interim Data from Phase 2 Study of UX001
in Hereditary Inclusion Body Myopathy
Study to continue to 48 weeks, followed by extension study testing higher dosage
Novato, CA—July 3, 2013—Ultragenyx Pharmaceutical Inc., a biotechnology company focused on developing treatments for rare and ultra-rare genetic disorders, announced interim 24-week data from a 48-week Phase 2 clinical study of UX001 in 47 patients with hereditary inclusion body myopathy (HIBM), a progressive muscle-wasting disease. The study compared treatment with a total daily dose of 6 grams or 3 grams of UX001 with placebo. UX001, an oral sialic acid extended-release (SA-ER) tablet, is designed to replace the deficient sialic acid substrate in patients with HIBM.
The data showed dose-dependent improvement in muscle strength relative to placebo in some muscle groups, particularly in the upper extremities at the 6-gram dose. These changes were statistically significant or trended towards significance, and were more pronounced in those patients that had greater walking ability at baseline, a predefined subset. Other clinical endpoints did not reveal changes at this interim assessment. Creatine kinase levels showed a trend to improvement in the 6-gram dose group compared with placebo. UX001 appeared to be well tolerated with no serious adverse events observed to date in either dose group.
“These early data suggest a modest dose-dependent improvement in muscle strength in HIBM patients treated with UX001 compared to a decline in placebo-treated patients,” said Emil Kakkis, MD, PhD, Chief Executive Officer of Ultragenyx. “We need to evaluate whether the observed treatment effect is sustained or increased over a longer 48-week period, and if higher dosing might further enhance the efficacy signal observed.”
The primary objective of the Phase 2 study is to evaluate safety, dose and potential pharmacodynamic effect of restoring sialylation of muscle in patients with a confirmed genetic mutation for HIBM. The study is also evaluating clinical measures of muscle strength, mobility, function, self-reported disability, and changes in quality of life. The study is taking place at four sites in the United States and Israel. Patients were randomized to receive placebo, 3 grams, or 6 grams per day of UX001, in three divided doses. At 24 weeks, placebo patients were randomized and crossed over into either of the two dose groups on a blinded basis. Patients will be evaluated again at 48 weeks,with final data anticipated around year-end. Following the 48-week analysis, the company plans to continue to treat these patients in an extension study with an increased dosage of UX001 based on the dose-dependence observed at week 24.

About Hereditary Inclusion Body Myopathy
Hereditary inclusion body myopathy (HIBM) is also known as GNE myopathy,
Quadriceps Sparing Myopathy (QSM), Inclusion Body Myopathy type 2, Distal Myopathy
with Rimmed Vacuoles (DMRV) and Nonaka myopathy. HIBM is a severe, adult-onset,
progressive, genetic neuromuscular disease caused by a defect in the biosynthetic
pathway for sialic acid (SA). Patients with HIBM typically begin to have weakness and
abnormal walking at 18 to 30 years of age. The body’s failure to produce enough sialic
acid causes muscles to slowly waste away and can lead to very severe disability within
10 to 20 years of diagnosis, with patients often ending up wheelchair-bound within that
time. There is currently no approved therapy.
About Ultragenyx
Ultragenyx is a privately held, clinical-stage biotechnology company committed to
bringing to market life-transforming therapeutics for patients with rare and ultra-rare
metabolic genetic diseases. The company, founded in 2010, is rapidly building a diverse
portfolio of products addressing diseases for which the unmet medical need is high, the
biology for treatment is clear, and for which there are no effective treatments.
Ultragenyx has two products in Phase 2 clinical trials, UX001 for the treatment of
hereditary inclusion body myopathy (HIBM), and UX007 for the treatment of fatty acid
oxidation disorders (FAOD). A third compound, UX003 for MPS 7 (Sly Syndrome), will
begin Phase 1/2 clinical trials later this year. The company is led by a management team
experienced in the development and commercialization of rare disease therapeutics.
Ultragenyx’ strategy is predicated upon time and cost-efficient drug development, with
the goal of delivering safe and effective therapies to patients with the utmost urgency.

For more information on Ultragenyx, please visit the company’s website at
www.ultragenyx.com.
http://www.ultragenyx.com/index.php?ht=a/GetDocumentAction/i/12770