Phase 1 Endometrial Cancer Trial, Recruiting
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 a specific type of lung cancer called non-squamous EGFR-Wt non-small cell lung cancer (a form of lung cancer where a particular gene marker, EGFR, is not mutated — confirm with trial site)
- People who have endometrial carcinoma (a cancer of the lining of the uterus)
- People who have ovarian cancer that has stopped responding to platinum-based treatment
Who may not be able to join:
- People who have cancer that has spread to the brain or spinal cord in a way that is not well controlled
- People who have a history of cancer spreading to the membranes surrounding the brain or spinal cord
- People who have an active infection — bacterial, viral, fungal, or parasitic — that is not under control
- People who have a known condition affecting the clear surface of the eye (cornea), or who have had a cornea transplant
- People who still have significant unresolved side effects from a previous cancer treatment
- People who have serious heart disease
- People whose heart's electrical activity shows a specific abnormality on an ECG reading (a QTcF measurement of 470 milliseconds or more — confirm with trial site)
- People who have a history of lung inflammation or scarring (pneumonitis or interstitial lung disease)
- People who are pregnant, breastfeeding, or planning to breastfeed during the study or within 30 days of the last dose of the study treatment
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.
Contact this trial
Principal Investigator: Margaret C Dugan, MD, Whitehawk Therapeutics
Phone: 888-392-9025
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
Where this trial is recruiting
Primary endpoints
Determine Maximum Tolerated Dose (MTD); Determine Maximum Administered Dose (MAD); Determine the Recommended Dose for Expansion (RDE)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.