Phase 2 Ovarian Cancer Trial, Recruiting NCT07610798 Sponsor: Shenzhen Ionova Life Sciences Co., Ltd. Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07610798
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:

  • People who have given written consent to participate.
  • Adults aged 18 years or older.
  • People who have been diagnosed (through laboratory testing of tumor tissue) with a solid tumor cancer that has spread or cannot be surgically removed, and whose tumor has a specific genetic change called KRAS G12D mutation.
  • People who are able to provide a stored tumor tissue sample or are willing to have a tumor biopsy taken before treatment begins.
  • People whose cancer has at least one measurable area that can be tracked on scans, according to standard measurement guidelines.
  • People who are expected to live for more than 3 months.
  • People who are generally well enough to carry out everyday activities with no or only minor limitations, as rated on a standard medical scale (confirm with trial site).
  • People whose bone marrow, liver, and kidneys are functioning adequately, as shown by blood tests.
  • People who are able to meet the trial's specific requirements around contraception.
  • People who have completed the required waiting periods after previous treatments, as specified in the trial protocol.

Who may not be able to join:

  • People who have had certain side effects from previous treatments within the 28 days before starting the study.
  • People who have a second, separate cancer diagnosis.
  • People who have a known allergy or sensitivity to the study drug or any of its ingredients.
  • People who have previously been treated with a targeted therapy that specifically targets the KRAS G12D mutation, or with a broader RAS-targeting therapy for this mutation.
  • People who have had major surgery within 28 days before the first dose of the study drug.
  • People who have cancer that has spread to the brain or the lining around the brain, and are experiencing symptoms from this.
  • People who have other serious ongoing health conditions, as assessed by the doctor running the trial.
  • People who have significant heart or blood vessel disease, as defined by the trial protocol (confirm with trial site).
  • People who have an abnormally prolonged measurement on a heart tracing (ECG) known as the QTcF interval.
  • People who are short of breath while at rest due to their cancer, or who need ongoing oxygen therapy for any medical reason.
  • People who have active tuberculosis (TB) affecting the lungs.
  • People who have a known history of a condition called interstitial lung disease, which involves scarring or inflammation in the lungs.
  • People who have previously had an organ transplant or a stem cell transplant from another person.
  • People who have had a serious infection within 28 days before the first dose of the study drug.
  • People who have a condition affecting their immune system, whether present from birth or developed over time.
  • People who are pregnant or breastfeeding.
  • People who have other health conditions or circumstances that the trial doctor believes could interfere with following the trial procedures.
  • People who are unwilling or unable to follow the procedures required by 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 12 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.

Contact this trial

Phone: 1 908 240 7514

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 2
Sponsor
Shenzhen Ionova Life Sciences Co., Ltd.
Registry
ClinicalTrials.gov
Start date
1 June 2026
Est. completion
1 May 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Phase 1: Number of participants with treatment-emergent adverse events (TEAEs) as assessed by Common Terminology Criteria for Adverse Events (CTCAE) version 5.0; Phase 1: Maximum tolerated dose (MTD); Phase 1: Recommended dose range (RDR) and/or Recommended Phase Ⅱ dose (RP2D); Phase 2: Evaluate overall response rate (ORR)

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: 12 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