Researchers are conducting a clinical trial of AGT-182, an investigational treatment for people with Hunter syndrome aka mucopolysaccharidosis II or mps 2
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Hunter Syndrome Trial - MPS 2 Treatment | breakingbarriershuntertrial.com Reviews
https://breakingbarriershuntertrial.com
Researchers are conducting a clinical trial of AGT-182, an investigational treatment for people with Hunter syndrome aka mucopolysaccharidosis II or mps 2
breakingbarriershuntertrial.com
What is Hunter Syndrome?
http://breakingbarriershuntertrial.com/what-is-hunter-syndrome
What is Hunter Syndrome? Also known as mucopolysaccharidosis type II, or MPS 2, is a rare, hereditary metabolic disorder. That primarily affects males; it is often severe and almost always progressive. In people with MPS syndrome, the iduronate-2-sulfatase (IDS) enzyme, which breaks down complex sugars, is missing or not working properly. This leads to an abnormal buildup of complex sugars in tissues throughout the body, including the brain, skeleton, joints, spinal cord, heart spleen, or liver.
Participating Physicians Hunter Syndrome (MPS 2) Trials
http://breakingbarriershuntertrial.com/participating-physicians
Participating Physicians – Hunter Syndrome Trial aka Mucopolysaccharidosis II or MPS2. Contact: Jacqueline Madden, PNP. SEE IF YOU QUALIFY. Children’s Hospital of Orange County. SEE IF YOU QUALIFY. Dr William R. Wilcox. SEE IF YOU QUALIFY. Ann and Robert H. Lurie Children’s. Dr Barbara K. Burton. SEE IF YOU QUALIFY. Dr Chester B. Whitley. SEE IF YOU QUALIFY. Of Pittsburgh of UPMC. Contact: Nadene Henderson, MS, CGC. SEE IF YOU QUALIFY. O and O Alpan, LLC. Fairfax, VA 22030. SEE IF YOU QUALIFY.
Hunter Syndrome Trial Blog
http://breakingbarriershuntertrial.com/category/hunter-syndrome-blog
Category Archives: Hunter Syndrome Trial Blog. Armagen Presents Data for Treatment of Hunter Syndrome MPS 2. July 14, 2016. Hunter Syndrome Trial Blog. In a recent press release, Armagen Inc. presented data from the first chorot of their Phase 1/2a sutyd of AGT-182, an investigational Enzyme Replacement Therapy that has received orphan drug designation from the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of Hunter Syndrome aka MPS 2. When GAG...
Hunter Syndrome Treatment - Hunter Disease Trial - AGT-182
http://breakingbarriershuntertrial.com/about-the-breaking-barriers-trial
The Breaking Barriers Clinical Trial of AGT-182 is a Phase 1 trial that will test the safety and determine a well-tolerated dose of AGT-182 for the treatment of patients with Hunter Syndrome. Participating in the Trial. Contact the clinical site via the contact form through this website. Call the clinical site directly. Ages 18 or older. Diagnosed with Hunter syndrome. Available for 8 weeks of investigational treatment. For more information on the trial, please view the Frequently Asked Questions.
Hunter Syndrome support groups - MPS 2 groups
http://breakingbarriershuntertrial.com/hunter-support-groups
Hunter Syndrome (MPS 2) Support Groups. If you or a loved one has Hunter syndrome. There are many dedicated organizations, Hunter Syndrome Support groups and other resources that foster education, support and research for these diseases. We encourage patients and caregivers living with Hunter syndrome to learn more about ongoing clinical trials for investigational therapies. Barbara Wedehase, MSW, CGC, Executive Director of the National MPS Society. CLICK THE LOGOS ABOVE TO BE LINKED TO THEIR WEBSITES.
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Hunter Syndrome (MPSII) « Hunter Syndrome Foundation
https://huntersyndromefoundation.org/what-is-hunter-syndrome-mpsii
A CURE IS WITHIN REACH! Research for a Cure. What is Gene Therapy? Hunter Syndrome (or Mucopolysaccharidosis/MPS II) is a rare condition affecting between 1 in 100,000 to 1 in 150,000 male births, although it is estimated that the grouping of MPS conditions collectively affect 1 in 25,000 births in the United States (MPS conditions include MPS I, II, III, IV, VI, VII and ML II and III). Unrelated children with Hunter Syndrome often look alike and have a distinctive coarseness in their facial features, in...
AGT-182 and AGT-181 and Clinical Trials | ArmaGen
http://armagen.com/our-pipeline/clinical-trials
Solving the Blood- Brain Barrier Dilemma. Ongoing Trial: AGT-182 Phase 1 Trial in Hunter Syndrome. The purpose of this Phase 1 clinical trial is to test the safety and determine a well-tolerated dose of the investigational treatment AGT-182 for male patients (age 18 years and older) with Hunter syndrome or mucopolysaccharidosis type II (MPS II). More information about the trial is available on www.breakingbarriershuntertrial.com. Or www.clinicaltrials.gov. Using the identifier number. ArmaGen is conducti...
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Hunter Syndrome Trial - MPS 2 Treatment
Click here to download the Newsletter:. Study Update from Armagen 3-18-16. Researchers are conducting a clinical trial of AGT-182. An investigational treatment for people with Hunter Syndrome aka mucopolysaccharidosis II or MPS 2. AGT-182 is an enzyme replacement therapy (ERT) designed to treat both the body-related (somatic) and central nervous system (CNS) symptoms and complications of Hunter syndrome. To find out how you or a loved one can participate in this trial. Ages 18 or older.
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