Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
FEMALE
NCT06618235

Trial of THEO-260 in Ovarian Cancer Patients

Led by Theolytics Limited · Updated on 2026-04-14

44

Participants Needed

4

Research Sites

192 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A research study evaluating a new oncolytic virus, THEO-260, in patients with advanced ovarian cancer. The trial will investigate different doses of THEO-260 administered intravenously to identify a dose that is safe, well tolerated, and exhibits preliminary evidence of anti tumour activity.

CONDITIONS

Official Title

Trial of THEO-260 in Ovarian Cancer Patients

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed advanced high grade serous or endometrioid cancer of the fallopian tube, primary peritoneum, or ovary
  • Disease resistant or refractory to platinum chemotherapy or no suitable standard treatment available
  • Life expectancy greater than 3 months
  • ECOG performance status of 0 or 1
  • Measurable disease according to RECIST V1.1 criteria
Not Eligible

You will not qualify if you...

  • Prior anti-cancer treatment within 28 days before first THEO-260 dose
  • Previous treatment with group B adenovirus
  • Participation in other investigational drug trials within 5 half-lives before first dose
  • Radiation therapy within 2 weeks before first dose or planned during study
  • Brain metastases or active central nervous system involvement
  • Uncontrolled pleural or pericardial effusion needing frequent drainage
  • History of pneumonitis or interstitial lung disease
  • QTcF interval 470 ms or higher or history of serious heart rhythm problems
  • Use of medications that prolong QTc interval
  • Active hepatitis, tuberculosis, SARS-CoV-2, or HIV infection
  • Recent serious infection requiring antibiotics
  • Known allergies to study drug components
  • Viral infection within 2 weeks before first dose
  • Active autoimmune disease needing recent systemic treatment
  • History of kidney injury or serious heart conditions
  • Left ventricular ejection fraction below 50%
  • Oxygen saturation below 92% on room air
  • Receipt of any vaccine within 28 days before first dose of THEO-260

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Centro Integral Oncológico Clara Campal (CIOCC) Hospital

Madrid, Spain

Actively Recruiting

2

The Beatson West of Scotland Cancer Centre

Glasgow, Scotland, United Kingdom

Actively Recruiting

3

Imperial College Healthcare NHS Trust, Hammersmith Hospital

London, United Kingdom

Actively Recruiting

4

Oxford University Hospitals NHS Foundation Trust, Churchill Hospital

Oxford, United Kingdom

Actively Recruiting

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Research Team

C

Clinical Trials

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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