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

Official title

A Phase 1, Open-Label, Dose Escalation, and Dose Expansion Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CT-01 as Monotherapy and Combination Therapy With Everolimus in Subjects With Intermediate or Advanced Hepatocellular Carcinoma (BCLC Stage B or C) With Preserved Liver Function (Child-Pugh Class A)

Overview

This is a Phase 1, open-label, multicenter, dose-escalation and dose-expansion study designed to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of CT-01, administered either as monotherapy or in combination with everolimus. The study population includes subjects with intermediate or advanced hepatocellular carcinoma (HCC) who have progressed on, or are intolerant to, at least one prior line of systemic treatment. All available standard-of-care therapies should have been received, if deemed appropriate by the investigator (unless contraindicated or considered inappropriate by the treating physician). Eligible subjects are classified as Barcelona Clinic Liver Cancer (BCLC) stage B or C and must not be amenable to curative treatment approaches. Only subjects with preserved liver function (Child-Pugh Class A, score 5-6) at screening are eligible. Approximately 141 participants will be enrolled across 20 sites in Europe (France, Spain, and Germany).

Detailed description

This is an open-label, multicenter study evaluating the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of CT-01 in subjects with advanced hepatocellular carcinoma (HCC). The study consists of two sequential parts.

Part 1 investigates CT-01 as monotherapy and includes a dose-escalation phase (Part 1A) followed by a dose-expansion phase (Part 1B). A Bayesian Optimal Interval (BOIN) design will be used, with up to seven predefined dose levels. Additional subjects may be enrolled to backfill dose levels of interest. Treatment will be administered in 28-day cycles, with dose-limiting toxicities (DLTs) assessed during Cycle 1. Dose decisions will be made by an Independent Data Monitoring Committee (IDMC), with input from a Safety Monitoring Committee (SMC).

Part 2 evaluates CT-01 in combination with everolimus and includes a dose-escalation phase (Part 2A) and a dose-expansion phase (Part 2B). Up to four dose levels are planned in Part 2A, with starting doses informed by Part 1 results. As in Part 1, DLTs will be assessed during Cycle 1 and reviewed by the IDMC and SMC.

Interventions

• Drug CT-01
  Investigational small-molecule degrader targeting transcription factors in HCC. Used as monotherapy or with everolimus in dose-escalation/expansion settings. Specific to protocol CT-01-CD-1.
• Drug EVEROLIMUS
  Approved mTOR inhibitor used in combination with CT-01 for HCC in this study. Evaluated for safety, tolerability, and PK/PD in CT-01-CD-1 protocol.

Primary outcome measures

• Number of participants with treatment-emergent adverse events (TEAEs) during CT-01 monotherapy [Time frame: Up to 12 months]
• Maximum tolerated dose (MTDm) of CT-01 monotherapy [Time frame: Up to 12 months]
• Number of participants with treatment-emergent adverse events (TEAEs) during CT-01 and everolimus combination therapy [Time frame: Up to 12 months]
• Maximum tolerated dose (MTDc) of CT-01 in combination with everolimus [Time frame: Up to 12 months]

Secondary outcome measures (12)

• Objective response rate (ORR) per RECIST v1.1 and mRECIST for CT-01 monotherapy [Time frame: Up to 12 months]
• Objective response rate (ORR) per RECIST v1.1 and mRECIST for CT-01 and everolimus [Time frame: Up to 12 months]
• Maximum plasma concentration (Cmax) [Time frame: Up to 12 months]
• Area under the concentration-time curve (AUC) [Time frame: Up to 12 months]
• Time to maximum concentration (Tmax) [Time frame: Up to 12 months]
• Change from baseline in MELD-Na score during combination therapy [Time frame: Up to 12 months]
• Change from baseline in Child-Pugh score during combination therapy [Time frame: Up to 12 months]
• Change from baseline in Albumin-Bilirubin (ALBI) score during combination therapy [Time frame: Up to 12 months]
• Change from baseline in lipid profile during combination therapy [Time frame: Up to 12 months]
• Change from baseline in serum glucose levels during combination therapy [Time frame: Up to 12 months]
• Change from baseline in serum alpha-fetoprotein (AFP) levels during combination therapy [Time frame: Up to 12 months]
• Terminal half-life (T1/2) [Time frame: Up to 12 months]

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:

• Documented to be surgically sterile or postmenopausal, or
• 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
• 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:

• Documented to be surgically sterile (vasectomy), or
• Practicing true abstinence during the treatment period and for 6 months after the last IMP administration, or
• 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).

• 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.
• Patients with a past or resolved HBV infection (defined as HBsAg positive and anti-HBc positive) are eligible.
• Patients positive for HCV antibody are eligible only if PCR is negative for HCV ribonucleic acid (RNA).
• Chronic HBV (HBsAg positive, undetectable or low HBV DNA, and normal ALT) is eligible if patients are receiving direct-acting antiviral treatment.
• 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).
• Patients with untreated HCV infection or have not completed treatment for HCV infection.
• 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).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Sequential

Masking

Open label

Primary purpose

Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06994572 · CT-01-CD-1

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗