Cellular Pharmacodynamics of Small Molecules in Lysosomal Storage Disorders

Overview

The purpose of this study is to evaluate the effect of small molecule therapy in primary cells derived from patients with lysosomal storage disease. The study will focus on activity of small molecules, in terms of measurements enzymes activity and level of substrates accumulations. Also, the effects of small molecules on cell function, including autophagy-lysosomal pathways, metabolism, mitochondrial function and immune reaction will be investigated.

Full Title of Study: “Cellular Pharmacodynamics of Small Molecules in Sanfilippo Disease(s) (MPS3) and Other Lysosomal Storage Disorders”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: July 2020

Detailed Description

Lysosomal storage diseases (LSD) often cause severe disability and have a devastating effect on quality of life. The current standard of care of a majority of LSD is enzyme replacement therapy (ERT). ERT, however, becomes less effective during the advanced stages of a disease. Another therapy is substrate reduction therapy (SRT). For example, SRT therapy for Gaucher disease with small molecules acts on ceramide synthesis pathway by decreasing production of the substrate. But, none of the above therapies are effective for treatment of a neuropathic form of LSD. Neurodegenerative changes in the central nervous system are a major problem in Sanfilippo disease. They cause severe disability and behavioral disturbance. This is the main reason for the absence of therapeutic options for MPS3 (Sanfilippo) patients. The future of neuropathic form of LSD therapy may lie in small molecules acting as agents for enzyme-enhancement therapy (EET). EET is based on the ability of small molecules to fold the misfolded mutant enzyme, activate autophagy-lysosomal pathways or mitochondrial function. This treatment approach has the potential to cross the CNS and carries the potential to treat the neurological symptoms of Sanfilippo disease or other types of LSD. The purpose of this study will evaluate the effect of small molecule therapy in primary cells derived from patients with lysosomal storage disease. The study will be focused on activity of small molecules, in terms of measurements enzymes activity and level of substrates accumulations. Also, the effects of small molecules on cell function, including autophagy-lysosomal pathways, metabolism, mitochondrial function and immune reaction will be investigated.

Arms, Groups and Cohorts

  • LSD
    • Subjects diagnosed or suspected to have any of the following lysosomal storage diseases: Gaucher disease, Fabry disease, Pompe disease, Mucopolysaccharidoses.
  • Control
    • Subjects with no known lysosomal storage disorder

Clinical Trial Outcome Measures

Primary Measures

  • Effect on enzyme activity
    • Time Frame: 24 months
    • To evaluate the effect of small molecules on level of enzyme activity in primary cells derived from patients using fluorometric enzyme assays.
  • Effect on substrate accumulation
    • Time Frame: 24 months
    • To evaluate the effect of small molecules on heparin sulfate accumulation and substrate accumulation in primary cells derived from patients using techniques like ELISA and mass spectrometry
  • Effect on autophagy-lysosomal pathway
    • Time Frame: 24 months
    • To evaluate the effect of small molecules on autophagy-lysosomal functions in primary cells derived from patients using commercially available assays
  • Effect on mitochondrial functions
    • Time Frame: 24 months
    • To evaluate the effect of small molecules on energy metabolism and mitochondrial functions in primary cells derived from patients using commercially available assay kits
  • Effect on immune and inflammatory response
    • Time Frame: 24 months
    • Examine the immune and inflammatory response to treatment with small molecules using flow cytometry based immunophenotyping

Participating in This Clinical Trial

Inclusion Criteria

Subjects with 1. confirmed diagnosis of any lysosomal storage disorder 2. family members with history of lysosomal storage disorders Exclusion Criteria:

Subjects excluded from the study include those who: 1. present with severe cognitive deficits impairing decision making 2. are unable to or for whom it is medically unsafe to withdraw from their current medications, such as subjects on SSRI s and other psychoactive drugs. The subjects on SSRIs may be included in the study only with an approval from the prescribing physician to discontinue their medications temporarily for the study. 3. are pregnant or nursing. All women of child bearing potential will undergo a pregnancy test. 4. have a history of neurologic conditions such as stroke or any focal brain lesion that may result in parkinonian manifestations. Individuals with such MRI findings will be excluded from the study.

Gender Eligibility: All

Minimum Age: N/A

Maximum Age: N/A

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Lysosomal and Rare Disorders Research and Treatment Center, Inc.
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Margarita M Ivanova, PhD, Principal Investigator, LDRTC
    • Ozlem Goker-Alpan, MD, Principal Investigator, LDRTC
    • Renuka Limgala, PhD, Principal Investigator, LDRTC
  • Overall Contact(s)
    • Margarita M Ivanova, PhD, 7032616220, mivanova@ldrtc.org

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