Peripheral Neuropathy Trial, Recruiting NCT06968975 Sponsor: Sanofi Condition: Peripheral Neuropathy
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Peripheral Neuropathy Trial, Recruiting

NCT06968975
Recruiting Not Applicable

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:

  • People who have been diagnosed with a condition called CIDP (a nerve disorder), confirmed by a neurologist, with no record suggesting that diagnosis was later ruled out
  • People who have been actively using at least one CIDP treatment for three months or more, with no sign that they stopped the treatment before their last neurologist visit — treatments that count include immunoglobulin, certain corticosteroids (but not low-dose prednisone or equivalent at 10mg or less per day on its own), plasma exchange, efgartigimod alfa, azathioprine, mycophenolate mofetil, cyclosporine, rituximab, or methotrexate
  • People who still have some ongoing physical impairment, disability, or neurological problems at the time of joining, based on a specific scoring scale used by the trial (confirm with trial site)
  • People who have signed a consent form agreeing to take part

Who may not be able to join:

  • People who are already taking part in another clinical trial that involves an investigational (unapproved) drug at the time of joining
  • People whose medical records show overactive reflexes during a neurological exam in the year before joining, recorded after their CIDP diagnosis was made
  • People who are under 18 years of age at the time of joining

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 15 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 800-633-1610

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
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
11 April 2025
Est. completion
17 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

I-RODS score at baseline; Variations of I-RODS score over the study duration; Variations of I-RODS score after treatment change; Annualized I-RODS response rate; Annualized I-RODS relapse rate

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: 15 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