Phase 3 Peripheral Neuropathy Trial, Recruiting NCT06920004 Sponsor: argenx Condition: Peripheral Neuropathy
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Phase 3 Peripheral Neuropathy Trial, Recruiting

NCT06920004
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:

  • People who have been diagnosed with CIDP (a nerve condition causing weakness and numbness) according to specific international medical guidelines from 2021
  • People who have the typical form of CIDP, or one of these specific variants: motor CIDP, multifocal CIDP (also called Lewis-Sumner syndrome), focal CIDP, or distal CIDP
  • People whose CIDP symptoms have improved with IVIg (an intravenous immune protein treatment) at some point in the last 5 years
  • People who are currently receiving regular IVIg treatment at a standard maintenance dose of at least 0.125 grams per kilogram of body weight per week
  • People who still have some ongoing disability and signs of active disease despite current treatment

Who may not be able to join:

  • People who have another known autoimmune condition, or any other health condition that could interfere with accurately assessing CIDP symptoms or could put them at unnecessary risk — including nerve damage caused by conditions other than CIDP
  • People whose CIDP diagnosis falls into the "possible CIDP" or "sensory CIDP" categories under the 2021 international guidelines
  • People who are currently using other long-acting treatments that affect the immune system (confirm with trial site for specific examples)

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 19 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: 857-350-4834

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
argenx
Registry
ClinicalTrials.gov
Start date
22 August 2025
Est. completion
1 September 2027

Where this trial is recruiting

🇦🇷 Argentina 🇦🇹 Austria 🇨🇿 Czechia 🇪🇪 Estonia 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇷🇸 Serbia 🇸🇬 Singapore 🇸🇰 Slovakia 🇸🇮 Slovenia 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇨🇭 Switzerland Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Reduction of ≥1 point compared with baseline in aINCAT score at 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: 19 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