Phase 1 Stomach Cancer Trial, Recruiting NCT06910657 Sponsor: ViroMissile, Inc. Condition: Stomach Cancer
Back to Stomach Cancer

Phase 1 Stomach Cancer Trial, Recruiting

NCT06910657
Recruiting Phase 1 🇦🇺 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:

  • Adults aged 18 or older.
  • People with advanced solid tumour cancers that have been confirmed by laboratory testing of tissue or cell samples, where the cancer has continued to grow despite standard treatment, or where no standard treatment exists.
  • People who are largely able to carry out daily activities with little or no restriction (as assessed by a standard medical scoring tool called ECOG, with a score of 0 or 1).
  • People whose cancer can be measured using standard medical imaging criteria (called RECIST v1.1).
  • People whose heart, liver, kidneys, and bone marrow are functioning adequately (confirm with trial site).
  • People who have waited at least 28 days since any major surgery, previous immunotherapy, or radiotherapy (minor procedures may have exceptions — confirm with trial site).
  • Women who could potentially become pregnant must have a negative pregnancy test before joining.
  • People who agree to use effective contraception throughout the treatment period and for 3 months afterwards.
  • People who are able to give informed consent and follow the requirements of the study.

Who may not be able to join:

  • People who have previously been treated with a type of cancer therapy called an oncolytic virus.
  • People with a current or recent vaccinia virus infection, or who have received a smallpox or monkeypox vaccination within the past 10 years.
  • People with an active, uncontrolled infection that currently requires treatment with systemic medicines (such as antibiotics or antifungals).
  • People with a history of hepatitis B, hepatitis C, or HIV, unless specific conditions set out in the trial protocol are met (confirm with trial site).
  • People who still have unresolved side effects of Grade 2 or higher from previous cancer treatments, with the exception of hair loss or certain stable ongoing conditions.
  • People with an active autoimmune disease causing symptoms that requires ongoing systemic treatment.
  • People with cancer that has spread to the brain or spinal cord (central nervous system) that is untreated or causing symptoms, unless it meets specific stability criteria outlined in the protocol (confirm with trial site).
  • People with significant heart disease, such as moderate to severe heart failure (NYHA Class III or IV).
  • People with a history of lung inflammation (pneumonitis) that required steroid treatment, or an ongoing lung condition called interstitial lung disease.
  • People who require long-term use of medicines that suppress the immune system.
  • People with severe skin conditions or a history of pancreatitis (inflammation of the pancreas).
  • People with bleeding disorders, or who have recently experienced a serious blood clot event.
  • People with any medical or mental health condition that could interfere with safely taking part in the study.

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 23 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: 858-886-7718

Australian sites

Royal North Shore Hospital, Saint Leonards, New South Wales
+61 (02) 9463 1199
Westmead Hospital, Westmead, New South Wales
+61 2 8890 9945
The Alfred Hospital, Melbourne, Victoria
+61 03 9076 3129

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
ViroMissile, Inc.
Registry
ClinicalTrials.gov
Start date
25 August 2025
Est. completion
31 January 2027

Where this trial is recruiting

🇦🇺 Australia 🇺🇸 United States

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

Primary endpoints

Incidence of Dose-Limiting Toxicities (DLTs); Safety and Tolerability of IDOV-Immune by Dose Level; Determination of the Maximum Tolerated Dose (MTD); Identification of Dose Level(s) for Further Clinical Evaluation

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: 23 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