Phase 2 Peripheral Neuropathy Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Pain Score
Can't join this trial?
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.