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Motor Neurone Disease - Systematic Multi-Arm Adaptive Randomised Trial

Motor Neurone Disease - Systematic Multi-Arm Adaptive Randomised Trial

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04302870
Acronym
MND-SMART
Enrollment
1150
Registered
2020-03-10
Start date
2020-02-27
Completion date
2030-12-01
Last updated
2026-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Brief summary

MND-SMART is investigating whether selected drugs can slow down the progression of motor neuron disease (MND) and improve survival. The study is 'multi-arm' meaning more than one treatment will be tested at the same time. The trial started with 3 arms; drug 1 (memantine), drug 2 (trazodone) and placebo (dummy drug). A third drug, amantadine, was added in April 2023. A fourth drug, tacrolimus, was added in March 2025 in Edinburgh and across all sites in April 2025. The first two drugs, memantine and trazodone, were removed from the trial in September 2023 due to lack of benefit. The trial currently has 4 recruiting arms; amantadine, liquid placebo (matched to amantadine), tacrolimus, and tablet placebo (matched to tacrolimus). This allows the evaluation of each drug versus placebo. Participants will be randomly allocated between the treatment arms they are eligible for. Medicines being tested are already approved for use in other conditions. MND-SMART has an 'adaptive' design. This means medicines being studied can change according to emerging results. Treatments shown to be ineffective can be dropped and new drugs can be added over the duration of the study. This will allow many treatments, over time, to be efficiently and definitively evaluated. The medicines being tested have been selected following a rigorous process involving a systematic, unbiased, and comprehensive review of past clinical trials data, as well as information from pre-clinical research (studies in laboratories), for MND and other related neurodegenerative disorders. Drugs have been ranked for inclusion in MND-SMART by a group of independent MND experts according to set criteria. These include consideration of how the drugs work, their safety profiles, and the quality of previous studies. New drugs will be selected for investigation in MND-SMART based on continuous review of constantly updated scientific evidence as well as findings from state-of-the-art human stem cell based drug discovery platforms. These can be added by substantial amendment to the protocol.

Detailed description

For further information, please visit: https://mnd-smart.org/

Interventions

DRUGMemantine Hydrochloride Oral Solution

Memantine hydrocholoride taken once daily

DRUGTrazodone Hydrochloride oral solution

Trazodone Hydrochloride taken once daily

Placebo taken once daily

DRUGAmantadine Hydrochloride Oral Solution

Amantadine Hydrochloride taken once daily

DRUGTacrolimus 1Mg Cap

Tacrolimus 1Mg overencapsulated tablet taken once daily

DRUGPlacebo capsule

Placebo taken once daily

Sponsors

University of Edinburgh
Lead SponsorOTHER
University College, London
CollaboratorOTHER
University of Warwick
CollaboratorOTHER
NHS Lothian
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants will be considered eligible for randomisation if they fulfil all the core inclusion criteria and none of the

Exclusion criteria

as defined below. In addition, investigators must simultaneously check and ensure participants do not meet any of the drug specific

Design outcomes

Primary

MeasureTime frameDescription
Survival18 monthsCo-primary outcome measure
Change in decline of ALS-FRS(R) over 18months18 monthsCo-primary outcome measure

Secondary

MeasureTime frameDescription
Safety and tolerability of IMPs18 monthsMeasured using adverse events
Cognition and behaviour18 monthsUsing Edinburgh Cognitive and Behavioural ALS Screen (ECAS)
Respiratory function - Forced vital capacity18 monthsChange in FVC
Changes in anxiety and depression18 monthsMeasured using the hospital anxiety and depression scale (HADS), scale range 0 - 42
King's ALS Clinical stage18 monthsTime to reach King's stage IV, scale range I - V
Changes in Quality of Life18 monthsMeasured using EQ-5D-5L

Countries

United Kingdom

Contacts

CONTACTProfessor Chandran
siddharthan.chandran@ed.ac.uk0131 465 9612
CONTACTAmy Stenson
astenson@exseed.ed.ac.uk0131 242 9122
STUDY_DIRECTORProfessor Chandran

University of Edinburgh

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026