Phase 1 Ovarian Cancer Trial, Recruiting NCT07503808 Sponsor: IDEAYA Biosciences Condition: Ovarian Cancer
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Phase 1 Ovarian Cancer Trial, Recruiting

NCT07503808
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:

  • You must be at least 18 years old (or the legal adult age in your country)
  • You have been diagnosed with one of these advanced, recurring, or spreading cancers that tests positive for specific proteins called B7-H3 and PTK7: non-small cell lung cancer, esophageal squamous cell cancer, endometrial cancer, a type of ovarian cancer (HGSOC), head and neck cancer (HNSCC), triple-negative breast cancer, colorectal cancer, or a type of prostate cancer (CRPC) — and your cancer has continued to grow or come back after at least one previous treatment, or you cannot tolerate further standard treatment
  • You have a stored tissue sample available from a previous biopsy or surgery for testing
  • Your cancer can be measured on a scan
  • You are in good enough general health to carry out daily activities with little to no limitation (confirmed by a standard health scoring system)
  • Your bone marrow, liver, kidneys, and other organs are functioning well enough
  • You are able to follow the study's requirements around contraception or barrier methods

Who may not be able to join:

  • You have brain or spinal fluid metastases that are causing symptoms
  • You have a cancer that started in the brain, or you have had another type of cancer within the past 2 years
  • You have cancer-related pain that is not well controlled
  • You have had a significant heart problem or a stroke within the past 6 months
  • You currently have an active infection that is not under control
  • You have a history of lung inflammation (pneumonitis), are currently being treated with steroids for a non-infectious lung condition, have suspected lung inflammation seen on recent scans, or have had a moderate to severe lung disease affecting your breathing in the past 3 months
  • You have had a serious infection requiring a hospital stay (such as blood infection or severe pneumonia) within the past 4 weeks
  • You have a weakened immune system or test positive for HIV at screening
  • You have a known or suspected hepatitis B or C infection
  • You have had active tuberculosis within the past year
  • You still have significant side effects from a previous cancer treatment that have not improved to a mild level (with the exception of some nerve-related symptoms) (confirm with trial site)
  • You have received chemotherapy within 3 weeks, immunotherapy or targeted cancer treatment within 3 weeks, or another experimental treatment within 4 weeks before starting this trial
  • You currently take or need to take certain medications or foods that strongly affect how the body processes drugs (confirm with trial site)
  • You have previously been treated with a drug that targets B7-H3 or PTK7 in a specific type of therapy called an antibody-drug conjugate (ADC)
  • You have had a specific type of cancer treatment called a topoisomerase I inhibitor within the past 6 months
  • You have had radiotherapy within the past 2 weeks
  • You have had major surgery or a significant injury within the past 4 weeks
  • You have received a live vaccine within the past 28 days or plan to receive one during the study
  • You are currently pregnant, breastfeeding, or planning to become pregnant during the study or within 7 months after your last dose
  • You have a known allergy to any ingredient in the study drug, or have had a severe allergic reaction to a similar type of drug before
  • You have certain eye conditions, including corneal ulcers or severe dry eye

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 30 June 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.

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Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
IDEAYA Biosciences
Registry
ClinicalTrials.gov
Start date
24 February 2026
Est. completion
30 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety and tolerability of IDE034 in Part 1 dose escalation; Safety and tolerability of IDE034 in Part 2 dose expansion; To evaluate preliminary anti-tumor activity of IDE034 in Part 2 dose expansion; To evaluate preliminary anti-tumor activity of IDE034 in Part 2 dose expansion

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: 30 June 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