Phase 1 Mesothelioma Trial, Recruiting NCT07705334 Sponsor: SHY Therapeutics Condition: Mesothelioma
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Phase 1 Mesothelioma Trial, Recruiting

NCT07705334
Recruiting Phase 1

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:

  • Adults aged 18 or older, of any gender
  • People whose doctors estimate they have more than 3 months to live
  • People who are largely able to carry out daily activities with little or no restriction (confirm with trial site what this means for a specific situation)
  • People who have advanced or metastatic solid tumours that have continued to grow despite standard treatments, or where standard treatments are not suitable — eligible cancer types include triple-negative breast cancer, hormone receptor-positive breast cancer, colon cancer, gastric (stomach) cancer, liver cancer (HCC), non-small cell lung cancer, mesothelioma, pancreatic cancer, hormone-resistant prostate cancer, and soft tissue sarcoma; other cancer types may be considered after discussion with the trial's medical team
  • People who have at least one tumour that can be measured using standard imaging methods
  • People who have a tumour that can be safely biopsied (a small tissue sample taken for testing)
  • People whose blood tests show the heart, liver, kidneys, and bone marrow are functioning adequately
  • People who are willing and able to give informed consent to participate
  • Women who could become pregnant must have a negative blood pregnancy test before starting and must use effective contraception throughout the trial and for 90 days after the last dose
  • Men must use barrier contraception or abstain from sex, and must not donate sperm, during the trial and for 90 days after the last dose
  • People with brain metastases (cancer that has spread to the brain) may be eligible if those metastases have been stable for at least 4 weeks following radiotherapy and steroid medication was stopped at least 14 days before joining

Who may not be able to join:

  • People with serious, high-risk heart or cardiovascular disease
  • People currently receiving other anti-cancer treatments
  • People who have had an active infection requiring treatment with antibiotics or antivirals within the 2 weeks before starting the trial
  • People with a history of a second, separate cancer (though certain exceptions apply, such as skin cancers or cancers that have been in remission for 2 or more years — confirm with trial site)
  • People with active hepatitis B, active hepatitis C, or poorly controlled HIV; people who have had a serious HIV-related infection within the past 12 months (note: people with well-controlled HIV may still be considered — confirm with trial site)
  • People who have had significantly reduced lung function within the 6 months before starting the trial
  • People who are pregnant or breastfeeding
  • People who have recently had radiotherapy, systemic cancer treatment, or participated in another clinical trial without a sufficient gap before joining this trial (confirm with trial site what timeframe applies)
  • People who have had major surgery within 4 weeks before starting the trial
  • People who are unable to swallow tablets, or who have a condition that affects how the gut absorbs medication
  • People with medical or psychiatric conditions that could affect their ability to follow the trial requirements or that could make the results difficult to interpret
  • People who still have significant side effects from previous cancer treatments (some exceptions may apply — confirm with trial site)
  • People with a clinically significant eye condition affecting the cornea
  • People who are unable to avoid certain medications that are not permitted during the 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 1: approximately ~10% 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

Phone: 619-985-2706

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 1
Sponsor
SHY Therapeutics
Registry
ClinicalTrials.gov
Start date
29 June 2026
Est. completion
15 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of Dose-Limiting Toxicities (DLTs), Adverse Events (AEs), and Serious Adverse Events (SAEs); Maximum Tolerated Dose (MTD); Recommended Phase 2 Dose (RP2D)

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