Phase 1 Breast Cancer Trial, By Invitation NCT07218003 Sponsor: Rondo Therapeutics Condition: Breast Cancer
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Phase 1 Breast Cancer Trial, By Invitation

NCT07218003
By Invitation Phase 1

voxsanity.com.au · Eligibility summary from public government registries · 18 August 2026 · not medical advice

Who may and may not 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 may be able to join

  • People with advanced or metastatic solid tumours that cannot be cured, where standard treatments have stopped working, are not tolerated, or where a doctor has determined the person is not suitable for standard treatment (or the person has chosen not to have it). Eligible cancer types include relapsed or treatment-resistant bladder cancer (including certain subtypes and cancers affecting the upper urinary tract), non-small cell lung cancer, head and neck squamous cell cancer, cervical cancer, stomach and gastro-oesophageal junction cancer, endometrial cancer, and triple-negative breast cancer.
  • For the bladder cancer group specifically: people who have had up to 2 prior treatments containing a drug called MMAE may be eligible, provided any existing nerve damage (peripheral neuropathy) is mild to moderate (Grade 2 or less).
  • People whose cancer can be measured using standard imaging criteria (called RECIST v1.1).
  • People whose organs (such as liver, kidneys, and bone marrow) are functioning adequately (confirm with trial site for specific thresholds).

Who may not be able to join

Each point below is a reason the trial team may not be able to accept someone. It is not a list of requirements to meet.

  • People who have previously received more than one treatment that targets a protein called Nectin-4, whether that treatment was an approved drug or an investigational one.
  • People with nerve damage (peripheral neuropathy) that is more than mild to moderate in severity (above Grade 2).
  • People who have a history of, or currently have, inflammatory skin conditions such as eczema or psoriasis that required or currently require biologic medications or oral steroid tablets to manage.

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 13 August 2026

GP referral letter

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Trial details

Status
By Invitation
Phase
Phase 1
Sponsor
Rondo Therapeutics
Registry
ClinicalTrials.gov
Start date
17 November 2025
Est. completion
28 February 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

All Arms: - Proportion of participants with adverse events (including dose limiting toxicities) as assessed by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0; Dose Optimization Arms: • Identify one or more recommended Phase 2 doses (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: 13 August 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