Not Yet RecruitingPhase 3ACTRN12624000423516

Efficacy of Reducing Fatigue In Relapsing Multiple Sclerosis: An Epstein Barr Virus Treatment Trial (FIRMS EBV)

Fatigue In Relapsing Multiple Sclerosis Epstein Barr Virus Treatment Trial (FIRMS EBV) - Comparing Spironolactone, Tenofovir Alafenamide and Placebo


Sponsor

The University of Sydney

Enrollment

240 participants

Start Date

May 1, 2024

Study Type

Interventional

Conditions

Summary

Existing Multiple Sclerosis (MS) therapies are effective at reducing MS relapses but there is currently no effective therapy for treating MS related fatigue. There is an understanding that chronic Epstein Barr Virus (EBV) infection of immune cells, called B lymphocytes, might be a driver of chronic symptoms in MS, such as fatigue. As such, this trial examines whether treating EBV infection can improve MS-related fatigue. The study tests two 'repurposed' anti-viral drugs, 'Tenofovir alafenamide' and 'Spironolactone', as an add-on to standard MS treatment for 16 weeks to see if fatigue can improve in participants with relapsing MS. We hypothesise that both Tenofovir alafenamide and Spironolactone will improve measures of fatigue in participants with relapsing MS compared to placebo.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 65 Yearss

Inclusion Criteria7

  • Male and female participants aged 18-65 years
  • Diagnosed with relapsing remitting Multiple Sclerosis (MS) by a neurologist
  • Expanded Disability Status Scale (EDSS) score of 6 within the last 12 months in the absence of an acute relapse or illness
  • Stable and have not received a new MS therapy in the preceding 8 weeks
  • Willingness to provide informed consent and willingness to participate and comply with the study requirements
  • Available to attend clinic visits within 1 week of each time point (baseline, Weeks 6, 16, and 20)
  • Clinical fatigue (evidenced by an FSS score greater than 4 on two occasions when completing the test serially online or in person over a fortnight)

Exclusion Criteria13

  • Participants treated with the MS disease-modifying therapy, cladribine (since TAF interacts with this drug) or the mood stabilizing agent, lithium (which interacts with spironolactone)
  • Treatment with angiotensin converting enzyme inhibitors or angiotensin 2 receptor blockers
  • A systemic medical disorder such as kidney disease or new diagnosis of hyper- or hypothyroidism OR any medical condition that may affect adherence to the trial intervention
  • Psychotropic medications if commenced < 4 weeks prior to study entry
  • Currently pregnant or lactating or if of child bearing potential, unwilling to take adequate contraception measures to prevent pregnancy for the duration of the clinical trial and for 2 weeks after trial completion
  • Commenced or are scheduled to commence iron supplementation
  • Acute suicidality (as per the Quick Inventory of Depressive Symptomology Tool) or a current diagnosis of substance abuse/dependence
  • Currently taking any illicit substances including any cannabis product (e.g. cannabis oil)
  • Recent gastrointestinal ulcers or renal stones
  • Epilepsy
  • Current use of any of the study drugs
  • Unable or unlikely to attend the required study visits at the required timepoints or unable to complete the study protocol
  • Lacks the capacity to consent as determined by the treating clinician

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Arm 1 - Spironolactone 25mg oral capsule twice daily for first week, then 50mg oral capsule twice daily for next 15 weeks. Arm 2 - Tenofovir Alafenamide (TAF) 25mg oral capsule daily for 16 weeks

Arm 1 - Spironolactone 25mg oral capsule twice daily for first week, then 50mg oral capsule twice daily for next 15 weeks. Arm 2 - Tenofovir Alafenamide (TAF) 25mg oral capsule daily for 16 weeks. Both interventions will be administered as an add-on to participants' usual MS treatments (disease-modifying therapies (DMT)) and they will continue taking these as prescribed by their treating doctor. Participants will return all unused study drug including empty bottles at study visits so that compliance can be checked.


Locations(12)

Concord Repatriation Hospital - Concord

NSW,QLD,TAS,WA,VIC, Australia

Brain and Mind Centre - University of Sydney - Camperdown

NSW,QLD,TAS,WA,VIC, Australia

The Alfred - Melbourne

NSW,QLD,TAS,WA,VIC, Australia

Royal North Shore Hospital - St Leonards

NSW,QLD,TAS,WA,VIC, Australia

John Hunter Hospital - New Lambton

NSW,QLD,TAS,WA,VIC, Australia

Launceston General Hospital - Launceston

NSW,QLD,TAS,WA,VIC, Australia

Gold Coast University Hospital - Southport

NSW,QLD,TAS,WA,VIC, Australia

Royal Brisbane & Womens Hospital - Herston

NSW,QLD,TAS,WA,VIC, Australia

Royal Melbourne Hospital - City campus - Parkville

NSW,QLD,TAS,WA,VIC, Australia

Liverpool Hospital - Liverpool

NSW,QLD,TAS,WA,VIC, Australia

Perron Institute for Neurological and Translational Science - Nedlands

NSW,QLD,TAS,WA,VIC, Australia

Austin Health - Austin Hospital - Heidelberg

NSW,QLD,TAS,WA,VIC, Australia

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12624000423516


Related Trials