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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT05231746

NCT05231746
Completed Phase 1

Who may be able to join

Who might be able to join this trial:

  • You are 18 years old or older
  • You are willing and able to give your signed agreement to take part in the study
  • You have at least one tumour or lesion that can be measured on a scan, based on standard medical criteria
  • You are able to carry out most daily activities with little or no restriction (confirm with trial site)
  • You are expected to live for at least 12 weeks
  • If you are able to have children (male or female), you agree to use contraception during the study and for at least 6 months after your last dose of the study treatment

Who may not be able to join:

  • You have had any cancer treatment in the 4 weeks before starting the study
  • You have had radiotherapy or major surgery in the 4 weeks before the screening visit
  • You still have significant side effects from a previous cancer treatment that have not mostly cleared up before starting the study
  • You have had a severe allergic reaction (grade 3 or higher) to a type of cancer immunotherapy drug called a checkpoint inhibitor
  • You have notable abnormal results in blood or other lab tests (confirm with trial site)
  • You have had another type of invasive cancer within the last 3 years
  • Your cancer has spread to your brain or spinal cord and is currently active
  • You need high doses of steroids or other medicines that suppress your immune system
  • You have a history of an autoimmune disease that needed medical treatment in the past 2 years
  • You currently have an active infection that requires treatment with antibiotics or antiviral/antifungal medicines
  • You currently have an active hepatitis B or hepatitis C infection
  • You have a known history of HIV infection
  • You currently have active tuberculosis (TB)
  • You have had a stroke, unstable chest pain, a heart attack, or severe heart problems in the 6 months before the screening visit
  • You have a history of certain lung conditions, such as pulmonary fibrosis or drug-related lung inflammation, or signs of active lung inflammation on a recent CT scan
  • You have previously had a stem cell transplant or an organ transplant from another person
  • You test positive for COVID-19 during the screening period
  • You have received a live vaccine within 30 days before the screening visit
  • You have another underlying medical condition that may affect your eligibility (confirm 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.

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.

Trial details

Status
Completed
Phase
Phase 1
Sponsor
STCube, Inc.
Registry
clinicaltrials_gov
Start date
18 April 2022
Est. completion
29 February 2024

Where this trial is recruiting

🇰🇷 South Korea 🇺🇸 United States

Primary endpoints

Incidence of DLTs; Incidence of AEs, SAEs, and abnormalities in Lab

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: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov