Trial of THEO-260 (Administered Via Intraperitoneal Route) in Ovarian Cancer Patients
- Registration Number
- NCT07211659
- Lead Sponsor
- Theolytics Limited
- Brief 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?
The clinical trial follows a dose escalation/ finding design where we will aim to establish a Recommended Phase 2 Dose (RP2D).
Participants will:
* Be administered 6 doses of THEO-260 via an intraperitoneal (IP) route of administration 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- Female
- Target Recruitment
- 18
- Confirmed histological diagnosis of advanced high grade serous or endometrioid cancer of the fallopian tube, primary peritoneum or ovary either on archival biopsy or fresh tumour biopsy.
- Platinum-resistant or refractory disease: platinum-resistance is defined as radiological progression within 6 months of last cycle of platinum treatment; platinum refractory disease is defined as radiological progression during the 3 months following the first dose with platinum treatment.
- Voluntary, written informed consent prior to trial procedures. Willingness and ability to comply with the protocol.
- Life expectancy of > 6 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 as per RECIST V1.1.
- Prior anti-cancer treatment or receipt of investigational product within 28 days or 5 half-lives, prior to first dose of THEO-260 or patients with unresolved serious toxic side-effects of prior chemotherapy or radiotherapy.
- Prior treatment with a group B adenovirus.
- Currently enrolled in a clinical trial of an IP or used any IP with 5 half-live before screening.
- Radiation therapy within 4 weeks of first dose of THEO-260.
- 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 IP, whichever was longer) with another drug prior to administration of IP.
- 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 (defined as having a positive hepatitis B surface antigen [HBsAg] test at screening) or hepatitis C.
- 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 IP.
- Patients with an active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs).
- Known heart failure New York Heart Association (NYHA) Class 2-4.
- Any major surgical procedure (planned or anticipated) (in the Investigator's judgement) within 4 weeks of the first dose of THEO-260 or within the anticipated treatment period.
- Known contra-indications or hypersensitivity to acetaminophen.
- Known alcohol consumption in excess of 2 units per day.
- Patients with a left ventricular ejection fraction (LVEF) <45%, unstable angina, serious uncontrolled cardiac arrhythmia, a myocardial infarction within 6 months prior to trial enrolment or a history of myocarditis.
- Patients with arterial oxygen saturation <92% on room air prior to first dose of investigational product.
- Patients who have received any live vaccines within 30 days prior to enrolment.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description THEO-260 THEO-260 -
- Primary Outcome Measures
Name Time Method Safety and tolerability of THEO-260 Until end of trial for a participant, estimated at 1 year Safety and tolerability will be assessed by:
Evaluation of DLTs and AEs during treatment and follow-up using National Cancer Institute (NCI) Common Terminology Criteria for AEs (CTCAE) v5.0 or American Society of Clinical Oncology (ASCO; for pneumonitis only) or American Society for Transplantation and Cellular Therapy (ASTCT; for cytokine release syndrome \[CRS\] only).Establish recommended Phase 2 dose (RP2D) for THEO-260 Until end of trial, estimated at 16 months after start of enrolment The totality of safety and efficacy data collected will be used to assess RP2D.
- Secondary Outcome Measures
Name Time Method Pharmacokinetic (PK) profile of THEO-260 Until Day 29 after first dose Assess PK profile (maximum concentration - Cmax) of THEO-260 in blood by qPCR.
Shedding of THEO-260 in saliva, urine, and faeces Until Day 29 after first dose Assess shedding of THEO-260 in buccal, urine and faecal samples by qPCR.
Risk of systemic cytokine release syndrome (CRS) after THEO-260 Until Day 29 after first dose Assess systemic CRS following administration of THEO-260 by measurement of key markers in blood.
Evaluate preliminary efficacy of THEO-260 - RECIST Until end of trial, estimated at 15 months after start of enrolment Determine response to THEO-260 as assessed by tumour imaging according to RECIST v1.1/iRECIST.
Evaluate preliminary efficacy of THEO-260 - CA125 Until end of trial, estimated at 16 months after start of enrolment Efficacy will also be measured by changes in cancer antigen 125 (CA-125).
Trial Locations
- Locations (1)
MD Anderson Cancer Center
🇺🇸Houston, Texas, United States
MD Anderson Cancer Center🇺🇸Houston, Texas, United StatesAmir JazaeriPrincipal Investigator