Phase 1 Stomach Cancer Trial, Recruiting NCT07358806 Sponsor: Oscotec Inc. Condition: Stomach Cancer
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Phase 1 Stomach Cancer Trial, Recruiting

NCT07358806
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 are 18 years of age or older (or 19 or older, depending on local rules) at the time of screening
  • You are willing and able to sign a consent form before any study-related procedures begin
  • Your doctor believes you are likely to live for more than 12 weeks
  • Your blood counts and organ function meet required levels — including healthy enough levels of white blood cells, platelets, red blood cells, liver function, and kidney function (confirm specific values with trial site)
  • Your heart is pumping blood at a normal or near-normal level (confirm with trial site)
  • You have at least one measurable tumor that can be tracked on scans
  • For Part A of the trial: You have an advanced solid tumor cancer and there are no good standard treatment options available or suitable for you, in your doctor's opinion
  • For Part B of the trial: You have an advanced solid tumor cancer and your doctor considers you a suitable candidate for treatment with a chemotherapy drug called docetaxel — this may include certain types of breast cancer, head and neck cancer, lung cancer, prostate cancer, or stomach/esophageal cancer
  • For Part B only: You have not previously been treated with docetaxel for advanced-stage disease

Who may not be able to join:

  • You have received cancer treatment (such as chemotherapy, immunotherapy, or targeted therapy) within approximately the last 28 days or longer, depending on the specific drug
  • You still have significant side effects from a previous cancer treatment that have not largely resolved (with some exceptions, such as stable nerve pain or stable hormone-related conditions — confirm with trial site)
  • You have previously been treated with a specific type of drug called an EP2 or EP4 antagonist (confirm with trial site)
  • You have had major surgery or extensive radiation therapy within the last 28 days, or limited palliative radiation within the last 7 days
  • You have active cancer that has spread to your brain and is causing symptoms (those with previously treated, stable, symptom-free brain metastases may still be eligible — confirm with trial site)
  • You are currently taking high-dose steroid medications (such as prednisone above a certain level) or immune-suppressing drugs within 7 days before starting the study (some exceptions apply — confirm with trial site)
  • You are currently taking certain anti-inflammatory medications such as NSAIDs, COX-2 inhibitors, or synthetic prostaglandins close to the start of the trial (low-dose aspirin may be permitted — confirm with trial site)
  • You are pregnant, breastfeeding, or planning to become pregnant during the study
  • You have another active cancer, or had a different cancer within the past 2 years (some early-stage or fully treated cancers may still be eligible — confirm with trial site)
  • You have a history of bleeding disorders, including bleeding in the stomach or digestive tract (those whose bleeding from their primary tumor is currently controlled may still be eligible — confirm with trial site)
  • You have a certain type of irregular heart rhythm or a heart condition that affects a specific electrical measurement of your heart called the QTc interval (confirm with trial site)
  • For Part B only: Your liver function tests are above certain levels at the same time (confirm specific values with trial site)

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.

Contact this trial

Phone: 82316287627

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
Oscotec Inc.
Registry
ClinicalTrials.gov
Start date
18 December 2025
Est. completion
1 December 2027

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

To evaluate the safety and tolerability by measuring the frequency and severity of adverse events, as assessed by CTCAE v5.0; Incidence of Dose-Limiting Toxicities (DLTs) for Determination of the Maximum Tolerated Dose (MTD); Incidence of adverse events and dose-limiting toxicities used to determine the recommended Phase 2 dose (RP2D) of OCT-598 (PART B only)

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