Phase 1 Oesophageal Cancer Trial, Recruiting NCT05238922 Sponsor: Incyte Corporation Condition: Oesophageal Cancer
Back to Oesophageal Cancer

Phase 1 Oesophageal Cancer Trial, Recruiting

NCT05238922
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:

  • You must be 18 years old or older at the time of signing the consent form
  • Doctors expect you to live for more than 12 weeks
  • You must be relatively active and able to care for yourself, with only mild limitations on daily activity (confirm with trial site)
  • Your cancer must have gotten worse despite standard treatment, or you could not tolerate standard treatment, or no standard treatment is available for your situation
  • You must have a stored tumor tissue sample available, or be willing to have a tumor biopsy taken before and during the trial
  • Depending on which part of the trial you join, you may need to have one of several specific cancer types, including ovarian, fallopian tube, or peritoneal cancer; endometrial or uterine cancer; stomach, stomach-esophagus junction, or esophageal cancer; triple-negative breast cancer; hormone receptor-positive/HER2-negative breast cancer; or other solid tumors (excluding bone cancers)
  • Your cancer must be measurable by CT or MRI scan (applies to certain parts of the trial)

Who may not be able to join:

  • You have a serious or uncontrolled heart condition
  • You have an abnormal heart tracing (ECG) that doctors consider medically significant
  • You currently have an active infection (such as bacterial, fungal, or viral) that requires ongoing medication
  • You have cancer that has spread to the brain or spinal cord that has not been treated or has continued to grow
  • You have another cancer that is currently active or has required treatment within the last 2 years
  • Your recent blood or lab test results fall outside acceptable ranges (confirm with trial site for specific values)
  • You have significant uncontrolled medical conditions, including serious liver or digestive system problems
  • You have not yet recovered from side effects of previous cancer treatments or complications from a recent surgery
  • You have previously been treated with a type of drug called a CDK2 inhibitor
  • You have had certain hormone therapies, targeted therapies, antibody treatments, or other specific cancer medications recently before joining (confirm exact timing with trial site)
  • You have had major surgery within the 28 days before starting the trial
  • You have had radiation therapy within the 28 days before starting the trial
  • You are currently taking part in another clinical trial or have taken an experimental drug recently (confirm exact timing with trial site)
  • You have an active hepatitis B or hepatitis C infection that needs treatment
  • You have a known history of HIV
  • You have had a severe allergic reaction to any ingredient in 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.

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 15 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: Liz Croft, MD, Incyte Corporation

Phone: 1.855.463.3463

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
Incyte Corporation
Registry
ClinicalTrials.gov
Start date
5 July 2022
Est. completion
27 July 2027

Where this trial is recruiting

🇫🇷 France 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands Puerto Rico 🇨🇭 Switzerland 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Part 1A : Occurrence of Dose Limiting Toxicities (DLTs); Number of Participants With Treatment Emergent Adverse Events (TEAEs); Number of Participants with Dose Interruptions due to TEAE; Number of Participants who Undergo Dose Reductions due to TEAE; Number of Participants Discontinue study due to TEAE

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: 15 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