Cited by 121Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and MyoclonusNanoparticle-Based Drug Delivery

Collaborative Development of 2-Hydroxypropyl-β-Cyclodextrin for the Treatment of Niemann-Pick Type C1 Disease

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Ottinger, Elizabeth, Kao, Mark, Carrillo-Carrasco, Nuria, Yanjanin, Nicole, Shankar, Roopa, Janssen, Marjo, Brewster, Marcus, Scott, Ilona +17 more·2014·Current Topics in Medicinal Chemistry

Abstract

In 2010, the National Institutes of Health (NIH) established the Therapeutics for Rare and Neglected Diseases (TRND) program within the National Center for Advancing Translational Sciences (NCATS), which was created to stimulate drug discovery and development for rare and neglected tropical diseases through a collaborative model between the NIH, academic scientists, nonprofit organizations, and pharmaceutical and biotechnology companies. This paper describes one of the first TRND programs, the development of 2-hydroxypropyl-β-cyclodextrin (HP-β-CD) for the treatment of Niemann-Pick disease type C1 (NPC1). NPC is a neurodegenerative, autosomal recessive rare disease caused by a mutation in either the NPC1 (about 95% of cases) or the NPC2 gene (about 5% of cases). These mutations affect the intracellular trafficking of cholesterol and other lipids, which leads to a progressive accumulation of unesterified cholesterol and glycosphingolipids in the CNS and visceral organs. Affected individuals typically exhibit ataxia, swallowing problems, seizures, and progressive impairment of motor and intellectual function in early childhood, and usually die in adolescence. There is no disease modifying therapy currently approved for NPC1 in the US. A collaborative drug development program has been established between TRND, public and private partners that has completed the pre-clinical development of HP-β-CD through IND filing for the current Phase I clinical trial that is underway. Here we discuss how this collaborative effort helped to overcome scientific, clinical and financial challenges facing the development of new drug treatments for rare and neglected diseases, and how it will incentivize the commercialization of HP-β-CD for the benefit of the NPC patient community.

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  1. [9]Rare Diseases and Orphan Products: Accelerating Research and Development 2011 The National Academies Press 21796826
  2. [65]Vol. 52 FR 19476, May 22, 1987, as amended at 57 FR 13248, Apr. 15, 1992

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Authors
Ottinger, E., Kao, M., Carrillo-Carrasco, N., Yanjanin, N., Shankar, R., Janssen, M., Brewster, M., Scott, I., Xu, X., Cradock, J., Terse, P., Dehdashti, S., Marugan, J., Zheng, W., Portilla, L., Hubbs, A., Pavan, W., Heiss, J., H.Vite, C., Walkley, S., Ory, D., Silber, S., Porter, F., Austin, C., & McKew, J.
Affiliations
  • National Institutes of Health (US)
  • Johnson & Johnson (United States) (US)
  • Yeshiva University (US)
Corresponding author
Ottinger, Elizabeth
Venue
Current Topics in Medicinal Chemistry
Published
2014-01-31
Volume
14
Issue
3
Pages
330-339
ISSN
1568-0266 (ISSN-L)
OpenAlex
W2146296797
Cited by
121
References
58
Citations by year
2026: 6 · 2025: 5 · 2024: 4 · 2023: 7 · 2022: 7 · 2021: 7 · 2020: 8 · 2019: 5 · 2018: 11 · 2017: 16 · 2016: 21 · 2015: 17 · 2014: 7
FWCI
13.52
Type
journal article
Language
en
Open access
Locations
  • Current Topics in Medicinal Chemistry (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health (UL1TR001425, ZIBTR000004)
  • National Institute of Neurological Disorders and Stroke (R01NS053677, R01NS081985)
  • National Center for Advancing Translational Sciences
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (P30HD071593)
Topics
  • Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
  • Health Sciences › Medicine › Rheumatology › Glycogen Storage Diseases and Myoclonus
  • Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
Keywords
hydroxypropyl-β-cyclodextrin, Niemann-Pick disease type C1, NPC1, NPC2, cholesterol transport, glycosphingolipid accumulation, rare disease drug development
MeSH terms
2-Hydroxypropyl-beta-cyclodextrin, Cooperative Behavior, Humans, National Institutes of Health (U.S.), United States, Rare Diseases, beta-Cyclodextrins, Niemann-Pick Disease, Type C, Drug Discovery, Neglected Diseases

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