Phase 2 Peripheral Neuropathy Trial, Recruiting NCT06798012 Sponsor: Takeda Condition: Peripheral Neuropathy
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Phase 2 Peripheral Neuropathy Trial, Recruiting

NCT06798012
Recruiting Phase 2

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 are 18 years of age or older at the time of signing the consent form
  • People who weigh 150 kilograms or less
  • People who have been diagnosed with typical CIDP (a nerve condition) by a neurologist who specialises in nerve and muscle diseases, confirmed using recognised 2021 diagnostic guidelines
  • People whose CIDP symptoms have previously improved, either partially or fully, with immunoglobulin (IgG) treatment
  • People whose CIDP has shown a meaningful worsening within the past 24 months — for example, symptoms got worse when treatment was reduced or stopped, required a higher dose to bring under control, or worsened near the end of a dosing period and then improved after the next dose
  • People who are currently on a stable dose of intravenous immunoglobulin (given through a drip), within a specific dose range every 2 to 6 weeks, with no change of more than 10% in dose or frequency in the 3 months before and during the screening period
  • People whose disability score on a standard nerve condition scale (called the INCAT score) falls between 0 and 7 at the time of screening

Who may not be able to join:

  • People who have been diagnosed with a variant form of CIDP (rather than the typical form), as defined by recognised 2021 guidelines
  • People whose nerve condition is caused by something other than CIDP, such as an inherited nerve disease (for example, Charcot-Marie-Tooth disease), an infection (such as Lyme disease), another medical condition (such as lupus, lymphoma, or diabetes-related nerve damage), or exposure to certain drugs, chemicals, or chemotherapy
  • People who have another long-term or serious condition affecting the nervous system — such as multiple sclerosis, Parkinson's disease, or stroke — that causes neurological symptoms or could affect how the trial measures CIDP
  • People who have taken certain immune-suppressing or immune-modifying medicines (other than intravenous immunoglobulin) for CIDP within the past 3 months or within 5 half-lives of that medicine (whichever is longer), or who have taken certain medicines that affect B-cells (such as rituximab) within the past 6 months — though people on a long-term stable dose of some of these medicines for a condition other than CIDP may still be considered (confirm with trial site)
  • People who have had a plasma exchange procedure within the past 3 months
  • People with a history of cancer who have not been in complete remission for at least 2 years, or who are currently receiving chemotherapy or radiotherapy — though people with certain treated skin cancers, cervical carcinoma in situ, or stable prostate cancer not needing treatment may still be considered (confirm with trial site)
  • People who have had a blood clot in a vein or artery (such as a stroke or pulmonary embolism) within the past 12 months
  • People who have a medical condition, abnormal test result, or other health finding that, in the opinion of the trial doctor, could make participation unsafe or interfere with completing the study
  • People who have taken part in another clinical trial involving an experimental treatment or device within the past 30 days, or who plan to do so during this trial

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 28 July 2026
Phase 2: approximately ~30% 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: Study Director, Takeda

Phone: +1-877-825-3327

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 2
Sponsor
Registry
ClinicalTrials.gov
Start date
14 May 2025
Est. completion
2 December 2027

Where this trial is recruiting

🇨🇦 Canada 🇨🇴 Colombia 🇺🇸 United States

Primary endpoints

Number of Participants With Improvement in Functional Ability 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: 28 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