Study of CT-01 as Monotherapy and Combination Therapy in Subjects With Intermediate or Advanced Hepatocellular Carcinoma

Launched by CAPTOR THERAPEUTICS S.A. · May 20, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called CT-01 for patients with intermediate or advanced liver cancer, known as hepatocellular carcinoma (HCC). The trial aims to explore how safe this treatment is, how well it works, and how it behaves in the body. It will involve participants who have already tried at least one other treatment for their cancer but did not see improvement or could not tolerate those treatments. To be eligible, participants must be at least 18 years old, have a specific type of liver function (Class A), and have tumors that are not suitable for curative treatments.

If you decide to participate, you will receive either CT-01 alone or CT-01 along with another medication called everolimus. The trial will take place at several locations across Europe, and around 141 people will be enrolled. Participants can expect to undergo regular check-ups and tests to monitor their health and how the treatment is working. It's important to note that this study is not yet recruiting participants, so it may take some time before enrollment begins.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Able to understand and willing to provide informed consent and able to comply with the study procedures and restrictions.
• • Are ≥18 years of age and of any gender at the time of screening.
• • Have confirmed histological and/or radiological diagnosis of HCC with a Child-Pugh Class A score of 5 to 6 points within 7 days of first dose of study drug.
• • Has BCLC stage B and are ineligible for or are refractory to locoregional therapy and not amenable to a curative treatment approach, or BCLC stage C and are not amenable to a curative treatment approach.
• • Have progressed on or are intolerant to ≥1 prior systemic standard of care treatment. All available standard of care treatments should have been received as prior systemic treatment if deemed appropriate by the investigator (unless such treatments are deemed contraindicated or inappropriate by the treating physician).
• • Have Eastern Cooperative Oncology Group (ECOG) score ≤1.
• • Have at least one measurable disease lesion per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 and/or modified RECIST (mRECIST), with a minimum of 1 target lesion in the liver at screening.
• * Female subjects may be enrolled if they refrain from donating eggs (ova, oocytes) for the purpose of reproduction during the treatment period and for 6 months after the treatment period and if they are:
• • 1. Documented to be surgically sterile or postmenopausal, or
• • 2. Practicing true abstinence for at least 28 days prior to investigational medical product (IMP) administration and for 6 months after the treatment period and having a negative pregnancy test prior dosing, or
• • 3. Willing and able to comply with two forms of contraception methods, including one physical barrier (condom or diaphragm) plus another method, such as adequate hormonal method (eg, contraceptive implants, injectables, oral contraceptives) or nonhormonal methods (eg, intrauterine device, spermicidal) during and for 6 months after the treatment period and having a negative pregnancy test prior dosing. Contraceptive use by women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
• * Male subjects with female partners of childbearing potential may be enrolled if they refrain from donating sperm during the treatment period and for 6 months after the last IMP administration and if they are:
• • 1. Documented to be surgically sterile (vasectomy), or
• • 2. Practicing true abstinence during the treatment period and for 6 months after the last IMP administration, or
• • 3. Willing and able to comply with two forms of contraception methods, including one physical barrier (condom or diaphragm) during the treatment period and for 6 months after the last IMP administration. Contraceptive use by men should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies
• Exclusion Criteria:
• • Have not recovered from toxicities to baseline or Grade ≤1 by CTCAE version 5.0 from prior anticancer therapy, except alopecia and sub-optimally treated nausea, vomiting, or diarrhea.
• • Have a history of liver transplant.
• • Any other active malignancy at time of screening or diagnosis of another malignancy within 2 years before screening that requires active treatment, except for superficial skin cancers, or localized, low grade tumors deemed cured and not treated with systemic therapy.
• • Have central nervous system (CNS) metastases or any other Grade \>2 CNS disorder. Subjects with CNS metastases who are stable on their treatment since a minimum of 4 weeks prior to screening are eligible.
• • Have recent esophageal or gastric variceal bleeding within 4 weeks prior to screening. Subjects with treated, stable, or small varices without bleeding within the 4 weeks prior to screening are eligible.
• • Have a history of symptomatic ascites requiring paracentesis within the past 3 months prior to screening.
• • Have a prior diagnosis of rhabdomyolysis from any cause.
• • Subjects with known retinal disease (eg, diabetic retinopathy, macular degeneration, retinal detachment/tear, etc).
• • Have a history of clinically significant cytokine release syndrome as assessed by the treating physician, clinically significant hypotension (defined as a blood pressure \[BP\] consistently \<90/60 mmHg and/or a BP associated with symptoms of hypotension (dizziness, fainting, orthostatic hypotension \[systolic BP drop of \>20 mmHg or diastolic BP drop of \>10 mmHg on orthostasis\]), symptomatic hypocalcemia and/or a calcium level \<1.5 mmol/L.
• • Have a history of pneumonitis or pericarditis.
• • Subjects who are not, in the opinion of the investigator, willing or able to comply with the protocol or who present a contraindication to any study procedure.
• * Have inadequate hematologic and end-organ function, defined as follows:
• • Hemoglobin \<8.5 g/dL
• • Absolute neutrophil count \<1,500 per mm3
• • Platelet count \<75,000 per mm3
• • Total bilirubin \>2 × ULN for the designated testing laboratory
• • AST or ALT \>5 × ULN
• • Serum creatinine \>1.5 × ULN
• • International normalized ratio (INR) \>1.7 × ULN
• • Glomerular filtration rate (GFR) \< 50 mL/min
• • Have imaging findings corresponding to HCC with ≥50% liver occupation, or clear invasion into the bile duct.
• • Have an active infection with the hepatitis B virus (HBV) or hepatitis C virus (HCV).
• • 1. Patients with acute hepatitis B infection are excluded. Acute Hepatitis B is defined based on the following serology profile: positive hepatitis B surface antigen (HBsAg positive), positive total hepatitis B core antibody (anti-HBc positive), IgM antibody positive to hepatitis B core antigen (IgM anti-HBc positive), and hepatitis B surface antibody negative (anti-HBs negative) test at screening.
• • 2. Patients with a past or resolved HBV infection (defined as HBsAg positive and anti-HBc positive) are eligible.
• • 3. Patients positive for HCV antibody are eligible only if PCR is negative for HCV ribonucleic acid (RNA).
• • 4. Chronic HBV (HBsAg positive, undetectable or low HBV DNA, and normal ALT) is eligible if patients are receiving direct-acting antiviral treatment.
• • 5. Patients with resolved hepatitis C infection are eligible. This is defined as undetectable or unquantifiable HCV RNA 12 weeks or longer after treatment completion (defined as a sustained virological response).
• • 6. Patients with untreated HCV infection or have not completed treatment for HCV infection.
• • 7. Patients with treated HCV infection but with a HCV viral load above the level of quantification.
• • Have a history of human immunodeficiency virus (HIV) infection.
• • Have life expectancy shorter than 3 months.
• • Have received any systemic anticancer treatment or any investigational treatment within 14 days or at least 5 half-lives of the treatment, whichever is shorter, prior to screening.
• • Are unable to take oral medications.
• • Have a known malabsorption syndrome.
• * Applicable to subjects enrolling in Part 2 only:
• • Are currently receiving treatment with the cytochrome P450 (CYP) 3A4 inhibitors (eg, azoles, clarithromycin, or grapefruit), CYP3A4 inducers (eg, rifampin, carbamazepine, phenytoin, or St. John's wort), or p-glycoprotein (P-gp) inhibitors or inducers (eg, verapamil, quinidine, amiodarone, diltiazem, erythromycin, cyclosporine, ketoconazole, ritonavir, or tamoxifen).
• • Subjects able to receive modified dose of the P-gp or CYP3A4 inhibitors based on everolimus drug label may be eligible at the discretion of the investigator in consultation with the sponsor and Medical Monitor.
• • Have a known intolerance or hypersensitivity to everolimus, its component (eg, lactose), or other rapamycin derivatives.
• • Subjects who are planned for elective surgery within 56 days of planned treatment Day 1 are excluded due to the risk of impaired wound healing with everolimus and the requirement to interrupt everolimus treatment per the everolimus SmPC. (Note: subjects who can delay elective surgery beyond Day 56 (Week 8, RECIST version 1.1 assessment) of study treatment are eligible for the study).