Phase 2 Ovarian Cancer 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 have been diagnosed (confirmed by laboratory testing of tumour tissue or cells) with an advanced solid tumour cancer that has stopped responding to standard treatments.
- People whose cancer can be measured using standard imaging criteria known as RECIST v1.1 or RANO-BM (confirm with trial site).
- People who have previously received a treatment that targets a protein called TROP2 — prior use of such therapy is permitted.
- People who are willing to provide stored tumour tissue samples, or to have a new biopsy taken before treatment if stored samples are not available.
- People who may also need to provide tissue samples during treatment, if the trial site's doctors consider this medically safe and appropriate.
- People who are generally well enough to carry out light activity and care for themselves, as measured by a standard health scale (ECOG score of 0 or 1).
- People whose blood counts and organ function meet specific minimum levels — including healthy enough levels of white blood cells, platelets, red blood cells, and liver enzyme readings (confirm exact values with trial site).
Who may not be able to join:
- People whose cancer has spread to the brain or spinal fluid and is currently active or getting worse. Note: people with brain metastases that have been treated and have remained stable for at least one month may still be considered eligible, provided certain conditions are met — such as having finished local brain treatment at least four weeks before starting the study drug, having no new or worsening neurological symptoms, and not needing steroids above a low stable dose or anti-seizure medications for symptom control (confirm with trial site).
- People who are still experiencing side effects from previous cancer treatments that are rated above a mild level (greater than Grade 1), not including hair loss or skin pigmentation changes.
- People who have received other systemic cancer treatments (including hormone-blocking therapies) too recently before the study start date — specifically within five half-lives of the drug or within four weeks, whichever period is shorter.
- People who are currently taking systemic steroid medications at a dose higher than 10 mg of prednisone per day (or an equivalent dose of another steroid), except in specific circumstances related to stable brain metastases as described above.
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: Rodrigo Ruiz-Soto, MD, AntibodyChem Biosciences
Phone: +1-615-975-7776
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
Safety of LCB84 alone and LCB84 in combination with an anti-PD-1 Ab (Phase 1 and 2); Recommended Phase 2 Dose of LCB84 alone and LCB84 in combination with an anti-PD-1 Ab (Phase 1); Objective Response Rate (Phase 2); Clinical Benefit Rate (Phase 2); Duration of Response (Phase 2); Time to Progression (Phase 2); Progression Free Survival (Phase 2); Overall Survival (Phase 2)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.