Phase 2 Ovarian Cancer Trial, Recruiting NCT07612891 Sponsor: Shenzhen Ionova Life Sciences Co., Ltd. Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT07612891
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:

  • You are 18 years of age or older
  • You have a solid tumor cancer that has been confirmed by a lab test, cannot be surgically removed, has spread or is locally advanced, and has either gotten worse after standard treatments, you could not tolerate standard treatments, or no standard treatments are available for your type of cancer
  • You are willing and able to provide a stored tumor tissue sample, or agree to have a tumor biopsy taken before treatment starts (for one part of the study)
  • Your cancer has at least one measurable area that can be tracked on scans, according to standard measurement guidelines
  • Your doctor expects you to live for more than 3 months
  • You are in relatively good general health and are able to carry out normal daily activities, with little or no limitation (as measured by a standard scale used in cancer trials)
  • Your bone marrow, liver, and kidneys are functioning well enough, as shown by blood tests
  • You agree to follow the study's specific requirements around contraception (birth control)
  • You have signed a form confirming you understand and agree to take part in the trial

Who may not be able to join:

  • You have a second, separate cancer diagnosis
  • Your cancer started in the brain or spinal cord, or you have cancer that has spread to the brain or spinal cord and previous local treatment there has not worked
  • You have received any cancer treatment, or taken part in another treatment trial, within the past 28 days
  • You have had major surgery within the past 28 days
  • You still have significant side effects from previous cancer treatments that have not cleared up enough
  • You have been diagnosed with a weakened immune system, or have taken immune-suppressing medications in the past 7 days
  • You have other serious ongoing health conditions, as assessed by the trial doctor
  • You have significant heart or blood vessel disease, as defined by the trial (confirm with trial site)
  • You have an abnormally long measurement on a heart tracing (ECG) called the QTcF interval (confirm with trial site)
  • You have a medical condition that is likely to affect how your body absorbs or digests the study medication
  • Your blood sugar (glucose) or blood pressure is not well controlled
  • Your blood potassium or sodium levels are significantly abnormal, as judged by the trial doctor
  • You have had a serious infection in the 14 days before starting the study drug
  • You have a confirmed infection with HIV, hepatitis B (HBV), or hepatitis C (HCV)
  • You are currently taking part in another clinical trial involving an investigational treatment
  • You have previously been treated with a type of drug called a CDK2 inhibitor
  • You have a known allergy or sensitivity to the study drug or any of its ingredients
  • You have had an organ transplant or tissue transplant from another person
  • You are unwilling or unable to follow the procedures required by the study
  • You have other serious health conditions, or there are other reasons the trial doctor considers you unsuitable for the study

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 6 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
4 July 2025
Est. completion
4 February 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Phase 1: Maximum tolerated dose (MTD); Phase 1: Recommended dose range (RDR); 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: 6 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