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      BioMarin Announces 20 Poster Presentations at Society for the Study of Inborn Errors of Metabolism (SSIEM) Symposium 2018

      Updated results from Phase 1/2 program for tralesinidase alfa (formerly BMN 250)

      BioMarin Pharmaceutical logo (PRNewsfoto/BioMarin Pharmaceutical Inc.)

      News provided by

      BioMarin Pharmaceutical Inc.

      Sep 05, 2018, 08:30 ET

      Share this article

      Share this article


      SAN RAFAEL, Calif., Sept. 5, 2018 /PRNewswire/ -- BioMarin Pharmaceutical Inc. (NASDAQ: BMRN) announced today that the company will present 20 poster presentations at the Society for the Study of Inborn Errors of Metabolism (SSIEM) Symposium 2018, which will be held on September 4-7 in Athens, Greece. 

      Listing of Posters and Presentations at Society for the Study of Inborn Errors of Metabolism 2018 Symposium

      Poster Presentations

      CLN2 Disease

      Title

      Authors

      Monitoring neuropsychological function in CLN2 disease

       

      Poster: #345

      Nickel M, Augustine E, Adams H, Baron I, Bjoraker K, Cohen-Pfeffer J, Delaney K, Elmerskog B, Newsom-Davis I, Rust S, Shapiro E, Tøssebro A, Schulz A

      Experiences of CLN2 disease diagnosis in the UK

       

      Poster: #357

      Burke D, Church H, Jackson M, Powers V, Tylee K

      Intracerebroventricular cerliponase alfa in children with CLN2 disease: interim results from an ongoing multicenter, multinational extension study

       

      Poster: #367

      Schulz A, de los Reyes E, Specchio N, Gissen P, Cahan H, Slasor P, Ajayi T, Jacoby D


      Phenylketonuria (PKU)

      Title

      Authors

      Burden of illness in adult patients with phenylketonuria and associated comorbidities – a retrospective database study in Germany

       

      Poster: #095

      Rutsch F, Muntau AC, Alvarez I, Lane P, Altevers J, Kohlscheen KM, Jacob C, Jain M, Schroeder C,

      Jha A, Treftz F

      Efficacy & safety of sapropterin in PKU patients <4 yrs: 3-year extension of SPARK open-label, randomized phase 3b trial

       

      Poster: #097

      Rutsch F, Burlina A, Eyskens F, Freisinger P,

      De Laet C, Leuzzi V, Sivri HS, Vijay S, Bal MO, Gramer G, Pazdírková R, Cleary M, Lotz-Havla AS, Mould DR, Lane P, Alvarez I, Muntau A

      Prevalence of comorbidities among phenylketonuria patients – a retrospective study of US health insurance claims data

       

      Poster: #098

      Burton B, Cederbaum S, Jurecki E, Lilienstein J, Alvarez I, Cohen-Pfeffer J, Irwin D, Levy H, Rohr

      The burden of illness in adults with phenylketonuria (PKU): interim analysis of a cross-sectional study

       

      Poster: #099

      Burton B, Longo N, Stuy M, Vockley J, van Backle J, Lane P, Alvarez I, Lilienstein J, Jurecki E

      International best practice recommendations for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria

       

      Poster: #117

      Bhattacharya K, Adams D, Belanger-Quintana A, Bushueva T, Cerone R, Chien N, Chiesa A, Coskun T, De la Heras Montero J, Feillet F, Katz R, Lagler F, Muntau A, Piazzon F, Rohr F, Spronsen F, Vargas P, Wilcox G

      Phase 3 PRISM clinical trials evaluating efficacy and safety of pegvaliase for treatment of adults with phenylketonuria

       

      Poster: #122

      Thomas J, Levy H, Amato S, Vockley G, Zori R, Dimmock C, Harding C, Bilder D, Weng HH, Olbertz J, Merilainen M, Rosen O, Gupta S, Gu K, Larimore K, Northrup H

      Long-term safety of induction, titration, and maintenance dosing of pegvaliase treatment in adults with phenylketonuria

       

      Poster: #123

      Burton B, Harding C, Thomas J, Longo N, Posner J, Dimmock D, Zori R, Weng H, Olbertz J, Gershman E, Rosen O, Gupta S, Jones S, Gu K, Vockley J

      Characterization of hypophenylalaninemia in pegvaliase treated adults with PKU

       

      Poster: #124

      Harding C, Thomas J, Burton B, Zori R, Dimmock D, Vockley J, Weng HH, Olbertz J, Gershman A,

      Rosen O, Jones S, Li M, Longo N

      An interim analysis of the KAMPER and PKUDOS registries: efficacy and safety of sapropterin before and during pregnancy

       

      Poster: #125

      Feillet F, Ficicioglu C, Lagler FB, Longo N, Alm J, Muntau AC, Burlina A, Belanger-Quintana A, Trefz FK, Kittus R, Jurecki E, Alvarez I, Lilienstein J, Burton B

      A meta-analysis of growth outcomes in phenylketonuria patients treated with phenylalanine-restricted diet + sapropterin

       

      Poster: #126

      Muntau A, Feillet F, Burton B, McDonald A, Wessel A, Alvarez I, Lilienstein J, Lane P, Jurecki E, Longo N


      Mucopolysaccharidosis (MPS)

      Title

      Authors

      Natural history data for young subjects with Sanfilippo syndrome type B (MPS IIIB)

       

      Poster: #315

      Harmatz P, Cleary M, de Castro Lopez MJ, Lee J, Lin S, Okur I, Ezgu F, Muschol N, Peters H, Solano Villarreal MS, Shaywitz AJ, Cahan H, Grover A, Maricich SM, Melton A, Smith L, Couce ML

      ICV-administered BMN 250 (NAGLU-IGF2) is well tolerated and reduces heparan sulfate accumulation in the CNS of subjects with Sanfilippo syndrome type B (MPS IIIB)

       

      Poster: #316

      Lin S, Cleary M, Couce ML, de Castro Lopez MJ, Harmatz P, Lee J, Okur I, Ezgu F, Peters H, Villarreal MS, Shaywitz AJ, Cahan H, Grover A, Maricich SM, Melton A, Smith L, Muschol N

      Critical care situations in patients with mucopolysaccharidosis (MPS)

       

      Poster: #321

      Stepien K, Geavorkian A, Hendriksz C, Lobzhanidze T, Perez-Lopez J, del Toro M, Vashakmadze N, Lampe C

      Transition from paediatric to adult care in patients with mucopolysaccharidosis (MPS)

       

      Poster: #324

      Lampe C, McNelly B, Geavorkian A, Hendriksz C, Lobzhanidze T, Perez-Lopez J, Vashakmadze N,

      del Toro M

      Mucopolysaccharidosis VI enzyme replacement therapy outcomes across the disease spectrum:  findings from the MPS VI clinical surveillance program

       

      Poster: #362

      Harmatz P, Lampe C, Teles EL, Parini R, Sharma R, Sivam D, Johnson J, Hawley S, Sisic Z

      Enzyme replacement therapy in patients with mucopolysaccharidosis VI: updated findings from the MPS VI clinical surveillance program

       

      Poster: #363

      Harmatz P, Lampe C, Leão-Teles E, Parini R, Sharma R, Sivam D, Johnson J, Sisic Z

      Mucopolysaccharidosis VI enzyme replacement therapy initiated in adulthood: findings from the MPS VI clinical surveillance program

       

      Poster: #364

      Lampe C, Harmatz, Leão-Teles E, Parini R, Sharma R, Sivam D, Johnson J, Hawley S, Sisic Z

      About BioMarin
      BioMarin is a global biotechnology company that develops and commercializes innovative therapies for people with serious and life-threatening rare disorders. The company's portfolio consists of seven commercialized products and multiple clinical and pre-clinical product candidates. 

      For additional information, please visit www.BMRN.com. Information on BioMarin's website is not incorporated by reference into this press release.

      BioMarin® is a registered trademark of BioMarin Pharmaceutical Inc.

      Contact:

      Investors: 

      Media:

      Traci McCarty

      Debra Charlesworth

      BioMarin Pharmaceutical Inc.

      BioMarin Pharmaceutical Inc.

      (415) 455-7558 

      (415) 455-7451

      SOURCE BioMarin Pharmaceutical Inc.

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