Phase 2 Peripheral Neuropathy Trial, Recruiting NCT07652879 Sponsor: Shanghai Changzheng Hospital Condition: Peripheral Neuropathy
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Phase 2 Peripheral Neuropathy Trial, Recruiting

NCT07652879
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 have been newly diagnosed with POEMS syndrome, confirmed using the 2023 Dispenzieri diagnostic criteria
  • People aged between 18 and 75 years
  • People who are reasonably mobile and able to carry out basic daily activities, with a life expectancy of more than 3 months (confirm with trial site regarding specific activity scale used)
  • People who do not currently have an active infection
  • People who have not previously received any treatment specifically for POEMS syndrome, other than corticosteroids (a type of anti-inflammatory medication)
  • People whose heart, liver, and kidneys are functioning well enough to meet specific laboratory test thresholds set by the trial
  • People whose blood count results — including white blood cells, platelets, and haemoglobin — meet the minimum levels required by the trial, without recent reliance on blood transfusions or growth factor medications
  • People who are able to swallow and take medications by mouth
  • People who have completed all required screening tests and assessments as outlined in the study
  • People who have signed a consent form agreeing to take part in chemotherapy as part of the trial

Who may not be able to join:

  • People whose POEMS syndrome also involves multiple myeloma, light chain amyloidosis, or a condition called Waldenström macroglobulinemia
  • People who are HIV-positive, or who have active hepatitis A, B, or C infection, or certain elevated hepatitis B virus levels in their blood
  • People who have serious ongoing health conditions such as heart failure, kidney failure, liver failure, bleeding disorders, a blood clot event within the past 6 months, uncontrolled diabetes, or a history of a specific type of bladder inflammation
  • People who have had an autoimmune disease (such as Crohn's disease, rheumatoid arthritis, or lupus) within the past 2 years that caused organ damage or needed ongoing medication to control it
  • People with severe active infections such as untreated tuberculosis or a serious fungal lung infection
  • People who currently have another type of cancer, with some exceptions for certain early-stage or previously cured cancers (confirm with trial site for specific exceptions)
  • People with epilepsy requiring medication, dementia, or other conditions affecting mental function that would make it difficult to understand or follow the study requirements
  • People whose circumstances — including substance use, psychological, or social factors — may interfere with participation or the reliability of study results
  • People who are pregnant or breastfeeding
  • People who the trial investigator considers unsuitable for the trial for any other reason

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 21 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: Haiyan He, Dr., Shanghai Changzheng Hospital

Phone: +86 13661513012

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
Shanghai Changzheng Hospital
Registry
ClinicalTrials.gov
Start date
15 June 2026
Est. completion
1 January 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall hematological response rate; Overall VEGF response rate; Overall neurological response 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: 21 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