Literature DB >> 18341400

Cellular therapy for childhood neurodegenerative disease. Part II: clinical trial design and implementation.

Nathan R Selden1, Daniel J Guillaume, Robert D Steiner, Stephen L Huhn.   

Abstract

Cellular replacement therapy attempts to improve functioning of the diseased human central nervous system (CNS). In this second installment of a 2-part review, the authors discuss the major challenges to the translation of in vitro and animal studies of neural stem cell (NSC) therapy in the clinical setting. This analysis details the problems unique to the design of clinical trials using human NSCs, outlines patient selection practices, describes surgical techniques for cellular transplantation, and reviews the regulatory issues and ethical concerns in trials involving neurologically impaired children.

Entities:  

Mesh:

Year:  2008        PMID: 18341400     DOI: 10.3171/FOC/2008/24/3-4/E22

Source DB:  PubMed          Journal:  Neurosurg Focus        ISSN: 1092-0684            Impact factor:   4.047


  9 in total

1.  Therapeutic effects of stem cells and substrate reduction in juvenile Sandhoff mice.

Authors:  J R Arthur; J P Lee; E Y Snyder; T N Seyfried
Journal:  Neurochem Res       Date:  2012-02-25       Impact factor: 3.996

2.  Methodology of clinical research in rare diseases: development of a research program in juvenile neuronal ceroid lipofuscinosis (JNCL) via creation of a patient registry and collaboration with patient advocates.

Authors:  Elisabeth A de Blieck; Erika F Augustine; Frederick J Marshall; Heather Adams; Jennifer Cialone; Leon Dure; Jennifer M Kwon; Nicole Newhouse; Katherine Rose; Paul G Rothberg; Amy Vierhile; Jonathan W Mink
Journal:  Contemp Clin Trials       Date:  2013-04-26       Impact factor: 2.226

Review 3.  Treating childhood traumatic brain injury with autologous stem cell therapy.

Authors:  Shyam Dewan; Samantha Schimmel; Cesar V Borlongan
Journal:  Expert Opin Biol Ther       Date:  2018-02-15       Impact factor: 4.388

4.  Intravenous high-dose enzyme replacement therapy with recombinant palmitoyl-protein thioesterase reduces visceral lysosomal storage and modestly prolongs survival in a preclinical mouse model of infantile neuronal ceroid lipofuscinosis.

Authors:  Jie Hu; Jui-Yun Lu; Andrew M S Wong; Linda S Hynan; Shari G Birnbaum; Denis S Yilmaz; Barbara M Streit; Ewelina M Lenartowicz; Thomas C M Thompson; Jonathan D Cooper; Sandra L Hofmann
Journal:  Mol Genet Metab       Date:  2012-05-22       Impact factor: 4.797

Review 5.  Progenitor cell-based treatment of the pediatric myelin disorders.

Authors:  Steven A Goldman
Journal:  Arch Neurol       Date:  2011-03-14

Review 6.  Stem cells and stroke: opportunities, challenges and strategies.

Authors:  Terry C Burns; Gary K Steinberg
Journal:  Expert Opin Biol Ther       Date:  2011-02-16       Impact factor: 4.388

7.  Experience, knowledge, and opinions about childhood genetic testing in Batten disease.

Authors:  Heather R Adams; Katherine Rose; Erika F Augustine; Jennifer M Kwon; Elisabeth A deBlieck; Frederick J Marshall; Amy Vierhile; Jonathan W Mink; Martha A Nance
Journal:  Mol Genet Metab       Date:  2013-11-04       Impact factor: 4.797

Review 8.  Mesenchymal Stem Cell-Based Therapy for Lysosomal Storage Diseases and Other Neurodegenerative Disorders.

Authors:  Shaza S Issa; Alisa A Shaimardanova; Victor V Valiullin; Albert A Rizvanov; Valeriya V Solovyeva
Journal:  Front Pharmacol       Date:  2022-03-02       Impact factor: 5.810

9.  An Implantable Micro-Caged Device for Direct Local Delivery of Agents.

Authors:  Alexander I Son; Justin D Opfermann; Caroline McCue; Julie Ziobro; John H Abrahams; Katherine Jones; Paul D Morton; Seiji Ishii; Chima Oluigbo; Axel Krieger; Judy S Liu; Kazue Hashimoto-Torii; Masaaki Torii
Journal:  Sci Rep       Date:  2017-12-15       Impact factor: 4.379

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.