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Multiple Sclerosis, Secondary ProgressivePhase 2NCT05013463

Hydroxychloroquine and Indapamide in SPMS

A Phase 2 study testing Hydroxychloroquine Pill and Indapamide Pill in people with Multiple Sclerosis, Secondary Progressive, run by University of Calgary at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this clinical trial is to determine if HCQ in a dose of 400mg daily and indapamide in a dose of 2.5mg daily can help in reducing the progression of disability in people with secondary progressive multiple sclerosis. The number of participants in this study will be 35. Read more about this study

Who is it for?
Ages 18 to 60 years
What is being tested?
Hydroxychloroquine Pill and Indapamide Pill
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
35 participants
Where
1 siteCanada
Study dates
1 Oct 2021to 1 Sep 2024
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Written informed consent obtained
  • Men and women aged 18 and 60 years inclusive
  • With SPMS, according to current diagnostic criteria
  • Screening Expanded Disability Status Scale score between 4.0 and 6.5 inclusive.
  • Screening timed 25-foot walk (average of two trials) of 9 seconds or more

Who cannot join

  • Individuals with retinopathy
  • Individuals whose screening ophthalmological exam shows retinopathy
  • Individuals with renal insufficiency (pre-existing or developing during the trial)
  • Individuals with significant hepatic impairment (pre-existing or developing during the trial)
  • Individuals with abnormal screening labs
  • Individuals with cardiac arrhythmia
Show all 16Show fewer
  • Individuals with a prolonged QT interval: individuals with frequency corrected QT (QTc) intervals of more than 450ms (men) or 470ms (women) at the screening examination will not be included in the study, and participants with QTc intervals of greater than 500ms on any of the other ECG examinations throughout the study will be excluded from the study.
  • Individuals with porphyria
  • Individuals with an allergy or other intolerability to HCQ or IND
  • Individuals who use Fampridine or 4-aminopyridine
  • Individuals who start Fampridine or 4-aminopyridine during the trial
  • Individuals who start Baclofen or Tizanidine during the trial
  • Individuals who increase the dose of Baclofen or Tizanidine during the trial
  • Individuals who receive treatment with Botulinum toxin in the leg muscles during the trial
  • Individuals who use siponimod, amiodarone, dapsone, digoxin or antimalarial drugs other than HCQ
  • Pregnant or breast-feeding women

Trial locations and contacts

1 site in 1 country.

Canada1 site, 1 recruiting
  • Foothills Medical Centre

    Calgary, Alberta, T2N 2T9

    Martha Rojas, (403) 944-4244, Martha.RojasZavala@ahs.ca

    Graziela Cerchiaro, (403) 944-4315, Graziela.Cerchiaro@ahs.ca

    Recruiting

Other trials in Canada

About this study

Official title: Open-label, Single-center, Single-arm Futility Trial Evaluating the Combination of Oral Hydroxychloroquine 200mg BID and Indapamide 2.5mg OD for Reducing Progression of Disability in People With Secondary Progressive Multiple Sclerosis (SPMS)

The purpose of this clinical trial is to determine if HCQ in a dose of 400mg daily and indapamide in a dose of 2.5mg daily can help in reducing the progression of disability in people with secondary progressive multiple sclerosis.

The number of participants in this study will be 35. A maximum of 42 people with SPMS will be included. The trial is funded through internal funding through the University of Calgary. There is no sponsorship from any pharmaceutical industry.

Read the detailed description

In patients with SPMS, there is ongoing slow and continuous loss of nerve cells, which causes damage to the brain and spinal cord. This ultimately becomes noticeable as slowly and continuously worsening disability. While the cause of this ongoing damage is unknown, it appears that at least part of the damage may be caused by cells in the brain called "microglia" (a type of immune cell that resides in the brain and spinal cord). These microglial cells can have beneficial roles, for instance when they clear away debris, but they can also cause damage to brain cells. In SPMS, microglial cells are often found to be in a state of activation, and it is currently believed that this constant activation of microglial cells is likely an important cause of the ongoing damage to brain cells. Another harmful process affecting patients with SPMS is "oxidative stress". Oxidative stress occurs when immune cells in the brain and spinal cord are activated and produce substances that may damage nerve cells. Current treatments for MS mostly are meant to prevent relapses and are beneficial in relapsing-remitting MS, but so far there are no treatments that benefit people with SPMS who do not experience relapses. Better therapies are needed for SPMS, and it is believed that treatments that reduce the activation of microglial cells and oxidative stress may be useful.

The medication Hydroxychloroquine (HCQ) reduces the activity of human microglia in laboratory experiments. Animal experiments also showed that treatment with HCQ reduces disease severity in an animal model of MS. HCQ, therefore, may also reduce the activity of microglia in people with SPMS, and hopefully prevent or slow down the progression of disability in SPMS. HCQ is currently approved in Canada to treat malaria and rheumatic diseases Systemic Lupus Erythematosus (SLE) and Rheumatoid Arthritis (RA). HCQ is available as a tablet that is usually taken two times per day. Doses up to 600mg per are used in clinical practice, but it is estimated that a dose of only 400mg daily, given as two doses of 200mg, will be sufficient to decrease the activity of microglia in patients with SPMS. HCQ is usually well tolerated.

Indapamide (IND) is a medication to treat high blood pressure that can reduce oxidative stress and improve the survival of nerve cells in laboratory studies. IND is currently approved to treat high blood pressure. IND is available in tablet form and is usually taken once a day, the most typical dose is 2.5mg. It is estimated that a dose of 2.5mg per day will be sufficient to treat oxidative stress in SPMS. IND is usually well tolerated.

Following a MinMax Simon-2-stage design, the study will require 35 patients with a complete 18 month follow-up. Presuming 20% drop-out, the investigators anticipate recruiting up to 42 patients. The trial will be conducted as follows: patients will continuously enter into the study until 35 patients have completed 18 months of follow-up with at least 75% adherence which will be measured by study drug count.

Being tested
Hydroxychloroquine Pill, Indapamide Pill
Medical subject headings
Multiple Sclerosis, Chronic Progressive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Hydroxychloroquine PillDrug

    Also called Plaquenil

    Oral Hydroxychloroquine, 200mg BID

  • Indapamide PillDrug

    Also called Lozol

    Oral Indapamide, 2.5 mg OD

Study groups in NCT05013463
Study groupRoleWhat they receive
Hydroxychloroquine and IndapamideExperimentalOral Hydroxychloroquine, 200mg BID Oral Indapamide, 2.5 mg OD
Receives: Drug: Hydroxychloroquine Pill; Drug: Indapamide Pill

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Timed 25-Foot Walk (T25FW)

    quantitative ambulation performance test

    Measured: Change in Timed 25-Foot Walk performance between the 6 month and 18 month visit

Secondary outcomes (5)
  1. 9-Hole Peg Test

    Brief, standardized, quantitative test of upper extremity

    Measured: baseline, 1 month follow-up, 6 months follow-up, 12 months follow-up, and 18 months follow-up

  2. Symbol Digit Modalities Test

    measures cognitive processing speed and working memory

    Measured: baseline, 1 month follow-up, 6 months follow-up, 12 months follow-up, and 18 months follow-up

  3. Functional Systems and Expanded Disability Status Scale (EDSS)

    Standard measure of neurologic impairment that is used to describe disability in MS. The neurological assessment comprises seven functional system on a scale of 0 (no disability) to 5 or 6 (more severe disability). EDSS steps 5.0 to 9.5 are defined by the impairment to walking.

    Measured: baseline, 1 month follow-up, 6 months follow-up, 12 months follow-up, and 18 months follow-up

  4. Modified Fatigue Impact Scale (MFIS)

    Structured, self-report questionnaire with 21 items concerning how fatigue impact patients quality of life, using a scale that ranges from 0 ("no problem") to 4 ("extreme problem"). Scores are then tallied to produce an overall score with a potential maximum of 160.

    Measured: baseline, 1 month follow-up, 6 months follow-up, 12 months follow-up, and 18 months follow-up

  5. Multiple Sclerosis Quality of Life Scale 54 item version

    54-item multidimensional health-related quality of life measure that combines both generic and MS-specific items

    Measured: baseline, 1 month follow-up, 6 months follow-up, 12 months follow-up, and 18 months follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Aug 2021
  2. Study start1 Oct 2021
  3. Primary completion1 Sep 2023 (estimated)
  4. Study completion1 Sep 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
Simon-2-stage MinMax design
Masking
None (open label)
Enrolment
35 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05013463
Sponsor's protocol ID
HCQ_IND_MS01
Status last verified
May 2022
First submitted
16 Aug 2021
Last updated
18 May 2022
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Hydroxychloroquine Pill and Indapamide Pill in people with Multiple Sclerosis, Secondary Progressive, run by University of Calgary at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 May 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Marcus Koch (4032106790, mwkoch@ucalgary.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Timed 25-Foot Walk (T25FW) (time frame: Change in Timed 25-Foot Walk performance between the 6 month and 18 month visit). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2022.

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