Trial of THEO-260 in Ovarian Cancer Patients

Trial Title: Trial of THEO-260 in Ovarian Cancer Patients

NCT ID: NCT06618235

Condition: Ovarian Cancer

Conditions: Official terms:
Ovarian Neoplasms
Carcinoma, Ovarian Epithelial

Study type: Interventional

Study phase: Phase 1/Phase 2

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Biological
Intervention name: THEO-260
Description: Oncolytic Virus
Arm group label: THEO-260

Summary: The goal of this clinical trial is to establish if THEO-260 is safe to administer to adult females with ovarian cancer. It will also aim to establish if THEO-260 is able to treat ovarian cancer. The main questions it aims to answer are: - What medical problems do participants have when taking THEO-260? - At what dose is THEO-260 both safe but also shows signs of being able to treat ovarian cancer? - At the selected dose, test THEO-260 is a wider group of participants to confirm the safety and ability to treat ovarian cancer. Part A will be the dose escalation/ finding part of the trial where we will aim to establish a Recommended Phase 2 Dose (RP2D). Part B will be where the recommended RP2D is given to a larger group of participants. Participants will: - Be administered 6 doses of THEO-260 over the course of 2 weeks. - They will then visit the clinic at regular intervals for check-ups and tests to monitor safety and THEO-260 ability to treat ovarian cancer.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Confirmed histological diagnosis of advanced high grade serous or endometrioid cancer of the fallopian tube, primary peritoneum or ovary either on archival biopsy (<1 year) or fresh tumour biopsy. - Voluntary, written informed consent prior to trial procedures. Willingness and ability to comply with the protocol. - Life expectancy of > 3 months. - Adequate haematological and organ function (parameters apply). - Non-pregnant and non-lactating and surgically sterile, or post-menopausal or abstinent or if of child-bearing potential will to use a highly effective form of contraception - where applicable. - ECOG performance status of 0 or 1. - Measurable disease per RECIST. enrolled with 0-8 weeks of radiological progression. - Part A: Platinum-resistant disease (radiological recurrence/ progression with 6 months of prior platinum treatment), primary platinum-refractory disease (recurrence/ progression during first line platinum treatment) and patients who are intolerant to or have no available SOC or SOC unacceptable/ unsuitable in the view of the Investigator. Part B: Advanced platinum-resistant disease: platinum-resistance as radiological recurrence/ progression within 6 months of prior platinum treatment or progression on SOC treatment or in intolerant to or has no available SOC or SOC unacceptable/ unsuitable in the view of the Investigator. Exclusion Criteria: - Prior anti-cancer treatment with 28 days or 5 half-lives whichever is longer, prior to first dose of THEO-260 or patients with unresolved or unstable serious toxic side-effects of prior chemotherapy or radiotherapy. - Prior treatment with a group B adenovirus. - Currently enrolled in a clinical trial of an IMP or used any IMP with 5 half-live before screening. - Radiation therapy with 2 weeks of first dose of THEO-260 and is scheduled to have radiation therapy during participation of trial. Short courses of palliative radiation therapy should be discussed with the Medical Monitor and Sponsor. - Clinical evidence of cerebral metastases or Central Nervous System (CNS) involvement including leptomeningeal disease. Patients with previous cerebral metastases must have no evidence of progression or haemorrhage after treatment and have been off dexamethasone for 4 weeks prior to first dose of THEO-260 with no ongoing requirement for dexamethasone or anti-epileptic drugs. Brain imaging in patients with a history of cerebral metastases or CNS involvement must not be older than 12 weeks (at the start of screening). Results of any unexpected or abnormal findings of brain imaging should be discussed with the Medical Monitor and Sponsor as part of the screening process. - Uncontrolled pleural effusion or pericardial effusion requiring recurrent drainage procedures (as defined as once monthly or more frequently). - Prior pneumonitis or history of interstitial lung disease. - Confirmed QTcF ≥470 ms on screening 12-lead ECG or history of Torsades de pointes or history of congenital long QT syndrome. - Concomitant medications that prolong the QTc interval and/or increase the risk for Torsades de Pointes that cannot be discontinued or substituted (within 5 half-lives or 14 days prior to the first dose of IMP, whichever was longer) with another drug prior to administration of IMP. - Any other concurrent severe and/or uncontrolled medical or surgical condition which, in the view of the Investigator, could compromise the patient's participation in the trial due to safety, compliance concerns or ability to evaluate response. - Patients with active hepatitis infection or hepatitis C. Patients with past hepatitis B virus (HBV) infection or resolved HBV infection. Patients positive for hepatitis C virus (HCV) antibodies are eligible only if polymerase chain reaction (PCR) is negative for HCV RNA. - Active infection with tuberculosis. Past or resolved tuberculosis is acceptable. - Active infection with severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2). - All patients should be tested for active SARS-Cov-2 infection and have a negative COVID-19 result within 3 days of Day 1 (e.g., if a patient tested positive in antigen testing but asymptomatic, the patient will need to be excluded). Active infection with SARS-Cov-2 confirmed as per site's standard way of testing. - Patients with active human immunodeficiency virus (HIV) infection or known history of HIV infection. - Active infection requiring IV antibiotics within 2 weeks prior to first dose of THEO-260, or long-term oral therapy for systemic infection. - Known contra-indications or hypersensitivity to the excipients of the IMP. - Viral syndrome diagnosed during the 2 weeks prior to first dose of THEO-260. - Conditions requiring treatment with immunosuppressant medications or corticosteroids (except for patients receiving inhaled corticosteroids at a stable dose for a diagnosis of asthma) within 4 weeks prior to the first dose of THEO-260. - Clinically or radiologically suspected, or evidence of, lymphangitic carcinomatosis. - Known risk of renal injury, including those with a past history of acute or sub-acute renal disease. - Known heart failure New York Heart Association (NYHA) Class 2-4 - Any major surgical procedure (planned or anticipated) (in the Investigator's judgement) within 2 weeks of the first dose of THEO-260 or within the anticipated treatment period. - Known contra-indications or hypersensitivity to the AxMP, paracetamol - Part B: Greater than a single line of anti-cancer therapy in the platinum-resistant setting. Prior treatment with paclitaxel (either alone or in combination with Bevacizumab) in the platinum-resistant setting is allowed.

Gender: Female

Minimum age: 18 Years

Maximum age: N/A

Healthy volunteers: No

Locations:

Facility:
Name: Imperial College Healthcare NHS Trust, Hammersmith Hospital

Address:
City: London
Country: United Kingdom

Status: Recruiting

Contact:
Last name: Jon Krell

Phone: +442033131000
Email: jonathankrell@doctors.org.uk

Start date: September 24, 2024

Completion date: July 2027

Lead sponsor:
Agency: Theolytics Limited
Agency class: Industry

Source: Theolytics Limited

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06618235