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Validation of the 18 kiloDalton Translocator Protein (TSPO) as a Novel Neuroimmunodulatory Target

Sponsor: Imperial College London

NCT ID: NCT03850301

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
XBD173 (drug), Etifoxine (drug)
How long the study runs
Study runs about 84 months (dates as stated)
About the drug or intervention
XBD173 — drug: 7 days treatment · Etifoxine — drug: 7 days treatment
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
35 Years to 65 Years
Who
All
Number of participants
44
Started
2018-01-01
Last checked
2024-10

Plain English Summary

What is this study?

  • • Testing a new treatment for multiple sclerosis
  • • NA - 44 participants
  • • In multiple sclerosis (MS) cells of the immune system attack the brain causing tissue damage

Who can take part?

  • • Ages 35 Years to 65 Years
  • • Diagnosed with multiple sclerosis

Where?

  • • London - Imperial College Healthcare NHS Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

In multiple sclerosis (MS) cells of the immune system attack the brain causing tissue damage. In secondary progressive MS (SPMS) these repeated immune attacks have stopped but despite this new damage continues to appear. TSPO is a protein found in the brain and cells of the immune system, whose levels increase during MS. The investigators would like to know whether drugs that bind TSPO could dampen the immune responses in patients with SPMS. The investigators will be testing two drugs that affect TSPO; etifoxine and XBD173. Subjects with SPMS will be recruited from neurology clinics at hospitals associated with Imperial College Healthcare NHS Trust. Healthy volunteers will also be recruited in order to provide a comparison to these patients. The volunteers recruited will be invited to the clinical research facility (CRF) at Hammersmith Hospital. The volunteers will take one of the two drugs every day for 7 days. The researchers will perform blood tests before the first dose and after the last dose to investigate the effects of the drugs, including the expression of genes and immune cell activity. This will allow the researchers to explore which of the two drugs produces the greatest changes in the amount of TSPO in the blood in MS patients relative to healthy controls.

More detail

The 18 kiloDalton Translocator Protein (TSPO) is a mitochondrial protein highly expressed in myeloid cells. While the full range of its functions are unknown, preclinical and in vitro studies provide suggestive evidence that TSPO ligands alter TSPO protein function to bias monocytes/macrophages and microglia towards reparative phenotypes. XBD173 and etifoxine are two TSPO ligands and represent two distinct chemotypes. Etifoxine is a benzoxaine, licenced in France (although not the UK) for the treatment of anxiety. XBD173 (Emapunil) is a phenylpurine that has recently been investigated for the treatment of anxiety, but is not licensed. The aim of this experimental medicine study is to test the hypothesis in humans that functional changes effected by TSPO can induce pro-inflammatory monocytes/macrophages and microglia to adopt a reparative phenotype. People with multiple sclerosis (MS) will be enrolled in this study because monocytes from MS patients have a chronic pro-inflammatory phenotype. Healthy volunteers (HVs) will also be enrolled to determine whether TSPO mediated effects are immune state dependant. The primary objective of this study is to determine the effects of TSPO ligand binding on monocyte/macrophage phenotype in humans. The secondary objectives are: a To characterise immunological responses in blood plasma and in circulating immune cell subsets of healthy volunteers and people with SPMS after TSPO functional changes induced by challenge ligand binding. b To explore the potential dependence of these pharmacodynamic responses on variation at rs6971 (a common polymorphism influencing ligand binding affinities in the TSPO protein) in the TSPO gene.

Multiple Sclerosis

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 35 Years - 65 Years
  • Who can join: All genders

Biomarkers mentioned

eGFR

What the study is looking for

  • ✓Capable of giving written agreement to take part, which includes compliance with the requirements and restrictions listed...
  • ✓Aged 35-65 years old
  • ✓Male subject must agree to use one of the contraception methods listed above.
  • ✓Willing to abstain from alcohol for the duration of dosing.
  • ✓Expanded Disability Status Scale (EDSS) \>3.5 \<6.5 (SPMS patients only)

Who cannot take part

  • ✗History of active neurological disease other than migraine or MS
  • ✗Clinically meaningful abnormalities in routine bloods including:
  • ✗eGFR \< 60ml/min
  • ✗Elevation of liver enzymes/liver blood test
  • ✗Prolonged prothrombin time
See the full criteria
Inclusion Criteria: 1. Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form. 2. Aged 35-65 years old 3. A female subject is eligible to participate if she is a) of non-childbearing potential, defined as pre-menopausal females with a documented tubal ligation or hysterectomy, or postmenopausal defined as 12 months of spontaneous amenorrhea or b) of childbearing potential but not pregnant (as determined by urinary pregnancy test on screening and on each study day) and willing to use one of the contraception methods listed below 4. Male subject must agree to use one of the contraception methods listed above. 5. Willing to abstain from alcohol for the duration of dosing. 6. Expanded Disability Status Scale (EDSS) \>3.5 \<6.5 (SPMS patients only) Exclusion Criteria: 1. History of active neurological disease other than migraine or MS 2. Clinically meaningful abnormalities in routine bloods including: * eGFR \< 60ml/min * Elevation of liver enzymes/bilirubin * Prolonged prothrombin time * Thrombocytopenia 3. Use of the following medications or therapies: * Immunosuppressive or immunomodulatory drugs within the last 6 months * Alemtuzumab or haematopeotic stem cell therapy * Central nervous system depressants (including opioid analgesics, barbiturates, sleeping pills, antihistamines, antipsychotics) * P450 CY3A4 inducers or inhibitors * oral contraceptives * oral anticoagulants or antiplatelet agents other than low dose aspirin * levothyroxine 4. Currently breastfeeding 5. Any clinical significant medical conditions that in the opinion of the investigator would compromise subjects' safety or compliance with study procedures. 6. History of any clinical condition which in the opinion of the principal investigator would compromise the scientific integrity of the study, such as some chronic systemic diseases affecting blood, liver or kidneys or endocrine system 7. Unwillingness or inability to follow the procedures outlined in the protocol 8. Subject is mentally or legally incapacitated 9. Contraindication to XBD173 use: • Hypersensitivity to the active substance or to any of the excipients 10. Contraindication to etifoxine use: * Myasthenia gravis * syndromes of glucose and galactose malabsorption or lactose deficiency

Where Is This Study? (1 UK site)

Imperial College Healthcare NHS Trust

London W12 0NN, United Kingdom

Recruiting
Site contact (verified)
Richard Nicholas, PhDr.nicholas@imperial.ac.uk

How to Get in Touch

David Owen, PhD

Sponsor contact

CONTACT

07801140800 d.owen@imperial.ac.uk

Lina Aimola, PhD

Sponsor contact

CONTACT

0207 594 1357 l.aimola@imperial.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2024-10