Phase 2 Ovarian Cancer Trial, Recruiting NCT06188520 Sponsor: AstraZeneca Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06188520
Recruiting Phase 2 🇦🇺 Australian site

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 are female and aged 18 or older.
  • People who have advanced solid tumours and have already received appropriate standard treatments for their tumour type, or where the treating doctor considers a clinical trial to be the best next option.
  • People whose cancer has spread or come back in the local region, and where scans or other objective measures show the disease has continued to grow or progress during or after the most recent treatment.
  • People who are generally well enough to carry out light activity (but not heavy physical work), with a life expectancy of at least 12 weeks.
  • People who have at least one tumour lesion that can be measured or assessed on scans at the start of the trial and monitored over time.

Who may not be able to join:

  • People who have received certain cancer treatments — including chemotherapy, other investigational drugs, or anti-cancer medicines — within 14 days or 5 half-lives of starting the trial drug (or 21 days for certain types), with some exceptions such as certain hormone-suppressing injections or bone-strengthening medicines.
  • People who are taking prescription or non-prescription medicines, or herbal products, that are known to significantly affect how certain drugs are broken down in the body (moderate or strong CYP3A4/5 inhibitors or inducers), if these cannot be stopped before the trial starts and kept stopped throughout.
  • People currently taking medicines known to carry a risk of a serious heart rhythm problem called Torsades de Pointes.
  • People who have received a limited course of radiotherapy for pain relief within 1 week of the planned first dose.
  • People who have had major surgery or a serious injury within 4 weeks before starting the trial, or who are expected to need major surgery or any surgery under general anaesthetic during the trial.
  • People who still have unresolved side effects of a moderate or severe level (Grade 2 or higher) from previous cancer treatment, with the exception of hair loss. People with stable mild-to-moderate nerve-related side effects (Grade 2 neuropathy) may still be considered (confirm with trial site).
  • People with life-threatening cancer spread to vital organs, or with uncontrolled cancer spread to the brain. People with treated and stable brain or spinal cord involvement who have been off steroids for at least 4 weeks may be considered (confirm with trial site).
  • People with serious uncontrolled health conditions, such as uncontrolled high blood pressure, active uncontrolled bleeding, serious active infections requiring intravenous antibiotics, or active hepatitis B, hepatitis C, or HIV requiring antiviral treatment.
  • People with certain heart conditions, including an abnormal heart rhythm measurement on ECG (resting QTcF greater than 470 milliseconds), significant abnormalities in heart rhythm or electrical conduction, or risk factors for dangerous heart rhythm problems such as symptomatic heart failure, a hereditary long QT condition, or a close family member who died suddenly and unexpectedly before age 40.
  • People with reduced heart pumping function (heart pumping less than 50% efficiency), or who have had a heart attack, unstable chest pain, significant heart failure, stroke, or mini-stroke in the past 6 months, or certain heart procedures such as bypass surgery, angioplasty, or a stent.
  • People with uncontrolled high blood pressure.
  • People whose blood test results show that bone marrow or organ function is not adequate (confirm with trial site for specific values).
  • People with persistent severe nausea and vomiting, uncontrolled long-term gut conditions, or a history of significant bowel removal surgery that could prevent the trial medicine from being properly absorbed.
  • People with a known allergy or hypersensitivity to the trial drug (AZD8421) or to drugs with a similar structure.
  • People who have previously been treated with AZD8421, or with any drug belonging to certain specific drug classes targeted by this trial (CDK2-selective inhibitors, PKMYT1 inhibitors, or WEE1 inhibitors).
  • People who are currently pregnant, breastfeeding, or planning to become pregnant. People of childbearing potential must agree to use at least one highly effective method of contraception.

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 20 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

Principal Investigator: Richard Baird, MD, PhD, Cambridge University Hospitals

Phone: 1-877-240-9479

Australian sites

Research Site, East Melbourne,

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
Registry
ClinicalTrials.gov
Start date
5 December 2023
Est. completion
4 August 2027

Where this trial is recruiting

🇦🇺 Australia 🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Incidence of dose limiting toxicities (DLTs) as defined in the protocol.; Incidence of AEs/SAEs; Clinically significant changes from baseline in clinical laboratory parameters, vital signs and ECGs.; Discontinuation of AZD8421 due to toxicity

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: 20 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