Actively Recruiting

Phase 2
Age: 18Years - 55Years
MALE
NCT03910738

TOTEM RRMS : TestOsterone TreatmEnt on Neuroprotection and Myelin Repair in Relapsing Remitting Multiple Sclerosis

Led by University Hospital, Strasbourg, France · Updated on 2025-06-29

40

Participants Needed

5

Research Sites

422 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Strasbourg, France

Lead Sponsor

B

Bayer

Collaborating Sponsor

AI-Summary

What this Trial Is About

Centra nervous system (CNF) damage in multiple sclerosis (MS), are mainly attributed to myelin destruction, axonal abnormalities and subsequent degeneration, and are responsible for serious deficiencies. Current therapies are focused on the treatment of inflammation with several types of anti-inflammatory agents. However, there is an urgent need for innovative therapies promoting neuroregeneration and particularly myelin repair. It has been demonstrated that testosterone can act through neural androgen receptors to promote proliferation and differentiation of oligodendrocyte precursors into mature oligodendrocytes in a cuprizone-induced animal model of demyelination. The rare clinical trials on testosterone are mainly exploratory. Here, we sought to demonstrate an effect of testosterone supplementation in testosterone-deficient patients in a multicenter, randomized, parallel-group, double-blind, placebo-controlled phase 2 trial. The main objective will be to determine the neuroprotective and remyelinating effects of testosterone using tensor diffusion imaging techniques and thalamic atrophy analyzes. As secondary objectives, we would like to study the impact of testosterone supplementation on other conventional and unconventional MRI parameters and on clinical outcomes (cognition, fatigue, quality of life, impact on work / activity and anxiety / depression).

CONDITIONS

Official Title

TOTEM RRMS : TestOsterone TreatmEnt on Neuroprotection and Myelin Repair in Relapsing Remitting Multiple Sclerosis

Who Can Participate

Age: 18Years - 55Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male between 18 and 55 years old
  • Affiliated to a social health insurance plan
  • Able to understand the study objectives and risks and comply with the protocol
  • Informed of prior medical exam results
  • Signed informed consent
  • Confirmed diagnosis of multiple sclerosis by revised McDonald criteria
  • Receiving natalizumab, fingolimod, ponesimod, ocrelizumab, or ofatumumab for at least one year before randomization
  • Switch between these therapies allowed if for non-neurological reasons
  • For ocrelizumab patients, must have received full doses for at least 2 years
  • Biological hypogonadism with serum total testosterone below 20 nmol/L
  • For natalizumab patients, negative or low JC virus status
  • No relapses in the year before inclusion
  • Disability score (EDSS) between 0 and 7 at selection
  • Stable neurological status in the month before randomization
Not Eligible

You will not qualify if you...

  • Progressive multiple sclerosis (primary or secondary)
  • Hypogonadism treated with androgens or with clinical symptoms
  • Prostate specific antigen above age-related thresholds
  • Hematocrit level above 54%
  • Unable or refusing to undergo MRI
  • Other diseases causing neurological symptoms or affecting evaluation
  • Signs of progressive multifocal leukoencephalopathy or confirmed leukoencephalopathy
  • Untreated sleep apnea
  • History of cancer or tumors of liver, heart, kidney, prostate, or breast
  • Cardiovascular, renal, hepatic, hematological, gastrointestinal, pulmonary, or uncontrolled diseases
  • Planning to father a child during the study
  • Chronic infectious diseases
  • Psychiatric or organic diseases impairing understanding or protocol compliance
  • History of hypersensitivity to study treatments or similar drugs
  • Participation in other experimental drug trials in past 6 months
  • Subject under legal protection or unable to give informed consent
  • Emergency situations or inability to understand study information

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 5 locations

1

CHU de Besançon

Besançon, France, 25000

Actively Recruiting

2

CHU Nancy

Nancy, France, 54000

Actively Recruiting

3

Hôpital Pitié-Salpêtrière

Paris, France, 75013

Actively Recruiting

4

CHU de Rennes/Pontchaillou

Rennes, France, 35000

Actively Recruiting

5

CHRU de Strasbourg

Strasbourg, France, 67000

Actively Recruiting

Loading map...

Research Team

L

Laurent D KREMER, MD

CONTACT

N

Nicolas COLLONGUES, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here