Phase 1 Ovarian Cancer Trial, Recruiting NCT06687070 Sponsor: Ascentage Pharma Group Inc. Condition: Ovarian Cancer
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Phase 1 Ovarian Cancer Trial, Recruiting

NCT06687070
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:

  • Part A only: People who have been diagnosed with non-small cell lung cancer or certain other advanced cancers that have a specific gene change (ALK or ROS1 gene fusion), confirmed by lab testing. Any gender may be eligible for this part.
  • Part B only: Women who have been diagnosed with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer, confirmed by lab testing.
  • People who have at least one tumor that can be measured on a scan.
  • People who are generally well enough to carry out normal daily activities with little or no difficulty (confirm with trial site regarding the specific fitness score required).
  • People who have a life expectancy of at least 3 months.
  • People whose side effects from any previous cancer treatment have mostly resolved to a mild level or better.
  • People who have adequate bone marrow, liver, kidney, and blood clotting function.
  • Women who are not pregnant and not breastfeeding at the time of joining.
  • People who are willing and able to understand and sign a consent form for the study.
  • People who are able to provide a tumor tissue sample (either recently collected or previously stored) before starting treatment.

Who may not be able to join:

  • People who have had major surgery, a significant injury, or a diagnostic biopsy recently before starting the trial (within specific timeframes — confirm with trial site).
  • People who have recently received systemic cancer treatments, including other experimental drugs (confirm with trial site regarding the required waiting period).
  • People who have had radiotherapy within 14 days before starting the trial.
  • People who have previously been treated with a type of drug called a FAK inhibitor.
  • People who have had a different type of cancer (other than ovarian cancer, for Part B participants) within the past 3 years before starting the trial.
  • People who have active cancer spread to the brain or spinal fluid (known as CNS metastases or cancerous meningitis).
  • People who have had a significant heart or stroke-related event within the past 6 months.
  • People who have fluid build-up around the lungs, heart, or abdomen that requires or has recently required draining.
  • People who have difficulty absorbing nutrients from food, or who are unable to swallow and take medication by mouth.
  • People who have a severe gastrointestinal (digestive system) condition.
  • People who have a serious or uncontrolled illness, or a chronic active infection.
  • People who have a known allergy to the trial drugs (APG-2449 or PLD) or any of their ingredients.
  • People who have previously received high cumulative doses of a certain class of chemotherapy drugs called anthracyclines (confirm with trial site for the specific dose threshold).
  • People who are currently taking certain medications that interact with specific liver enzymes or drug transport systems in the body (confirm with trial site for the specific medications involved).
  • People who the trial investigator believes should not participate for other medical or safety reasons.

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 28 July 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.

Contact this trial

Principal Investigator: Jundong Li, M.D., Sun Yat-Sen University Cancer Center

Phone: +86-20-28068501

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 1
Sponsor
Ascentage Pharma Group Inc.
Registry
ClinicalTrials.gov
Start date
17 December 2024
Est. completion
1 May 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Treatment-related adverse events per NCI-CTCAE version 5.0.; Dose Limiting Toxicity(DLT).

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: 28 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