Phase 2 Peripheral Neuropathy Trial, Recruiting NCT07558733 Sponsor: Faeth Therapeutics Condition: Peripheral Neuropathy
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Phase 2 Peripheral Neuropathy Trial, Recruiting

NCT07558733
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:

  • You have been diagnosed with breast cancer that is hormone receptor-positive (HR+) and HER2-negative, confirmed by a lab test on tissue.
  • Your cancer has spread or come back in a way that cannot be treated with surgery or radiation to try to cure it.
  • You have already received at least one previous treatment for your cancer (such as a drug or therapy).
  • You have at least one area of cancer that can be measured or tracked on scans.
  • You are generally able to carry out daily activities with little or no limitation (confirm with trial site regarding the specific fitness level required).
  • You are female, not pregnant, and not breastfeeding — and you are either past menopause, have had a procedure to prevent pregnancy, or agree to use effective birth control during the trial.

Who may not be able to join:

  • Your breast cancer is classified as "triple-negative" breast cancer.
  • Your cancer has spread to the brain or spinal cord, unless that was already treated, and you have not needed steroid medications for it for at least 4 weeks before starting this trial.
  • You have had another type of cancer in the past 2 years, with some exceptions such as certain skin cancers or fully removed early-stage cancers (confirm with trial site for your specific situation).
  • You have a feeding tube into your stomach, a condition that affects how your body absorbs food or medication, a blockage in your bowel, or any other issue that might affect how the study drug is absorbed.
  • You have a significant heart or cardiovascular condition (confirm with trial site for specifics).
  • You have an active infection that is not under control.
  • You are currently taking part in another clinical trial that involves a treatment.
  • You have had radiation therapy within the last 21 days before starting this trial.
  • You have previously been treated with certain targeted drugs that affect specific cell-signalling pathways (known as PI3K, AKT, mTORC1/2, or dual PI3K/mTOR inhibitors — confirm with trial site if unsure whether your past treatments apply).
  • You are currently taking, or need to take, certain medications that strongly affect how the liver processes drugs (known as strong CYP3A4 or CYP1A2 inhibitors or inducers — confirm with trial site regarding your current medications).
  • Your heart's electrical activity shows a specific irregularity on an ECG called a prolonged QTc interval above a certain level (confirm with trial site for details).
  • You have Type 1 or Type 2 diabetes and use insulin to manage it.

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 2 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Faeth Therapeutics
Registry
ClinicalTrials.gov
Start date
1 April 2026
Est. completion
1 May 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety and tolerability of drugs by assessment of adverse events (AEs) / serious adverse events (SAEs)

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: 2 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