Phase 3 Multiple Sclerosis Trial, Recruiting NCT07321093 Sponsor: Biocad Condition: Multiple Sclerosis
Back to Multiple Sclerosis

Phase 3 Multiple Sclerosis Trial, Recruiting

NCT07321093
Recruiting Phase 3

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be willing and able to sign a consent form agreeing to take part in the study.
  • You must be between 18 and 55 years old (inclusive) at the time of signing the consent form.
  • You must have been diagnosed with multiple sclerosis (MS) using a recognised set of medical guidelines called the McDonald criteria (2017 version).
  • You must have the relapsing-remitting type of MS, where symptoms come and go in episodes.
  • Your MS disability level must fall within a certain range on a standard scoring scale (confirm with trial site for exact details).
  • You must have had at least one MS relapse (flare-up) in the past 12 months, OR two relapses in the past 24 months, OR at least one active area seen on a specific type of brain scan (MRI) plus one relapse in the past 24 months.
  • A blood test must show that you have had a previous chickenpox infection or vaccination (presence of certain antibodies).
  • Your MS symptoms must have been stable for at least 30 days before signing the consent form.
  • You must be willing to stop taking any current MS medications from the day you receive your first dose of the trial drug and throughout the study.
  • You must be able to follow all the steps and procedures required by the study, in the opinion of the study doctor.
  • You and your partner (if they could become pregnant) must be willing to use reliable contraception from signing the consent form, throughout the study, and for 5 months after your last dose of the trial drug.

Who may not be able to join:

  • You have the primary progressive or secondary progressive type of MS.
  • You have had MS for more than 10 years and have a very low disability score on the standard MS scale (confirm with trial site for exact details).
  • You have a particularly severe or aggressive form of MS (confirm with trial site).
  • You have another medical condition that could make it difficult to accurately assess your MS symptoms.
  • You are unable to have a good-quality MRI scan, or you have a reason why you cannot have an MRI or be given the contrast dye used during the scan.
  • You have another condition that requires you to take steroid tablets or immune-suppressing medicines during the study (other than for MS).
  • You have a history of a serious brain infection called progressive multifocal leukoencephalopathy (PML).
  • You have an active or worsening infection found during the screening process that could put your safety at risk during the study.
  • You have other health conditions that could affect the assessment of your MS or significantly increase your risk of side effects during the study.
  • You have a known problem with alcohol or drug addiction, or you are currently showing signs of this.
  • You have a history of severe depression, or your score on a standard depression questionnaire is at or above a certain level at the time of screening.
  • You have had a cancer diagnosis within the past 5 years before screening.
  • You have a diagnosis of HIV, hepatitis B, or hepatitis C.
  • It is not possible to take blood from a vein for the study tests.
  • You are pregnant, breastfeeding, planning to become pregnant, or planning to donate eggs during the study or within 5 months after your last dose of the trial drug.
  • You have had a severe allergic or life-threatening reaction to certain types of antibody-based medicines in the past (confirm with trial site for exact details).
  • You have previously taken certain medicines or received certain treatments that are not allowed in this study (confirm with trial site for the full list).
  • Your blood test results fall outside the ranges considered acceptable for this study (confirm with trial site for exact details).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: +7 (812) 380 49 33

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Biocad
Registry
ClinicalTrials.gov
Start date
1 November 2025
Est. completion
1 December 2028

Where this trial is recruiting

🇷🇺 Russia

Primary endpoints

Total number of T1 gadolinium-enhancing (Gd+) lesions up to Week 24.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov