Phase 2 Peripheral Neuropathy Trial, Recruiting NCT04970121 Sponsor: Yan Yang, MD, Ph.D Condition: Peripheral Neuropathy
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Phase 2 Peripheral Neuropathy Trial, Recruiting

NCT04970121
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 willing and able to sign a consent form and follow the study requirements
  • People aged 18 to 75 years old (inclusive) at the time of signing the consent form, of any gender
  • People who have been diagnosed with a malignant solid tumour, confirmed by laboratory tissue or cell testing
  • People who have previously received chemotherapy that included a type of drug called a taxane
  • People who have nerve pain or numbness (called chemotherapy-induced peripheral neuropathy) rated at a certain level of severity, as measured by standard medical scales (confirm with trial site)
  • People whose general physical functioning is rated at a certain level on a standard scale used by doctors (ECOG score of 0–2, meaning able to carry out daily activities with at most limited self-care ability — confirm with trial site)
  • People with an expected survival of at least 3 months
  • People whose blood counts, liver function, and kidney function meet specific levels shown in blood tests taken during screening
  • Women who are not breastfeeding and have a negative pregnancy test result
  • People who are able to use effective contraception from signing the consent form until at least 30 days after the last dose of the study treatment
  • People who are already taking certain pain medicines (such as opioids, paracetamol, aspirin, or anti-inflammatory drugs) may still be considered, provided the dose has been stable for the two weeks before joining

Who may not be able to join:

  • People who have a known allergy or sensitivity to duloxetine or any of its ingredients
  • People who are currently taking other medicines known to affect serotonin (a chemical messenger in the brain) levels
  • People who need to take a type of antidepressant called a monoamine oxidase inhibitor (MAOI)
  • People who have active cancer that has spread to the brain or the lining of the brain
  • People who have a type of eye condition called uncontrolled closed-angle glaucoma
  • People whose nerve symptoms are caused by physical pressure on a nerve (such as from a tumour pressing on it)
  • People who have a mental health condition, epilepsy, mania, depression with thoughts of suicide, dementia, or issues with alcohol or drug use that could affect their ability to follow the trial requirements
  • People who have certain heart or cardiovascular conditions, including moderate-to-severe heart failure, unstable chest pain, a heart attack or stroke in the past 6 months, certain heart rhythm problems, a blocked major vein near the heart, abnormal heart electrical readings above certain thresholds, or high blood pressure not controlled by medication
  • People with other medical conditions or history that could interfere with the trial results
  • People where the trial doctor or sponsor believes taking part would not be in that person's best interest

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 26 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: Yan Yang, M.D.,Ph.D, The First Affiliated Hospital of Bengbu Medical University

Phone: +86-0552-3086178

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
Yan Yang, MD, Ph.D
Registry
ClinicalTrials.gov
Start date
21 August 2021
Est. completion
1 July 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pain Score

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: 26 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