Phase 1 Ovarian Cancer Trial, Recruiting NCT07371104 Sponsor: Daewoong Pharmaceutical Co. LTD. Condition: Ovarian Cancer
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Phase 1 Ovarian Cancer Trial, Recruiting

NCT07371104
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:

  • Women aged 19 years or older at the time of signing the consent form
  • People diagnosed with advanced high-grade ovarian cancer that has a BRCA gene mutation
  • People who have already been taking olaparib 300 mg (two 150 mg tablets) twice daily by mouth for at least 10 days in a row, OR people whose treating doctor considers a stable dose of olaparib 300 mg twice daily to be appropriate for them
  • People with a life expectancy of at least 12 weeks, as estimated by their doctor
  • People with a Body Mass Index (BMI) — a measure of body weight relative to height — between 18.50 and 30.00 kg/m² at the time of screening

Who may not be able to join:

  • People who have had a serious allergic reaction to olaparib or any of its ingredients
  • People currently living with certain serious health conditions, including lung inflammation (pneumonitis), a blood or bone marrow disorder called myelodysplastic syndrome or acute myeloid leukaemia, severe liver disease, an active uncontrolled infection or systemic illness, or active hepatitis B, hepatitis C, HIV, or syphilis
  • People who have received radiation therapy within 4 weeks before screening
  • People who have received any other anti-cancer treatment within 4 weeks before screening
  • People who have had major surgery within 4 weeks before screening, or who have not fully recovered from a previous major surgery
  • People who have lost approximately 350 mL of blood or more in the 12 weeks before screening

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 26 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.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
Daewoong Pharmaceutical Co. LTD.
Registry
ClinicalTrials.gov
Start date
22 April 2026
Est. completion
1 March 2027

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Cmax; AUCtau

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: 26 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