Phase 1 Peripheral Neuropathy Trial, Recruiting NCT05584631 Sponsor: Rutgers, The State University of New Jersey Condition: Peripheral Neuropathy
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Phase 1 Peripheral Neuropathy Trial, Recruiting

NCT05584631
Recruiting Phase 1

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:

  • Adults over 18 years old who have been diagnosed with a condition called CIDP (a nerve disorder), based on recognised European diagnostic guidelines.
  • People whose current intravenous immunoglobulin (IVIG) dose, when converted to a weekly under-the-skin (subcutaneous) dose, falls within a specific range of 0.2 to 0.4 mg per kilogram of body weight.

Who may not be able to join:

  • People who are receiving IVIG treatment for any condition other than CIDP.
  • People who have liver problems, specifically liver enzyme levels more than three times the normal upper limit, or reduced kidney function below a certain level (confirm with trial site).
  • People who have an active cancer of any kind.
  • People who have diabetes.
  • People who have a condition called myasthenia gravis (a muscle weakness disorder).
  • People who have a weakened immune system or immune deficiency condition.
  • People who have another autoimmune disease (a condition where the immune system attacks the body).

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 14 July 2026
Phase 1: approximately ~10% 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

Principal Investigator: Luigi Brunetti, PhD, Rutgers, The State University of New Jersey

Phone: 2016385868

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 1
Sponsor
Rutgers, The State University of New Jersey
Registry
ClinicalTrials.gov
Start date
11 September 2022
Est. completion
1 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Assessment of drug half-life; Assessment of immune globulin G serum concentration after intravenous immune globulin G administration; Assessment of immune globulin G serum concentration after subcutaneous immune globulin G administration

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: 14 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