A Safety and Pharmacokinetics Study of RC220 Combined With Doxorubicin in Adult Participants With Solid Tumours.

Launched by RACE ONCOLOGY LTD · Feb 3, 2025

Keywords

ClinConnect Summary

This clinical trial is evaluating a new treatment called RC220, both on its own and combined with a standard chemotherapy drug called doxorubicin, for adults with advanced solid tumors. The study aims to find out how safe this combination is and how well it works. It is divided into two parts: the first part will test different doses of the combination to determine the highest dose that patients can tolerate, while the second part will focus on confirming its safety and exploring its effects on the tumors and heart protection.

To be eligible for this trial, participants must be at least 18 years old, have a life expectancy of at least three months, and have measurable solid tumors that have not been previously treated with anthracyclines (like doxorubicin). Participants will need to provide informed consent and meet certain health criteria, including having adequate blood, liver, and kidney function. Throughout the trial, participants can expect regular check-ins to monitor their health and any side effects. It’s important to note that this study is currently recruiting participants, and anyone interested should discuss this opportunity with their healthcare provider to see if it’s a good fit for them.

Gender

ALL

Eligibility criteria

• Inclusion Criteria (For Part 1 and Part 2):
• • 1. Able to give voluntary informed consent and understand the study and are willing to follow and complete all the study required procedures.
• • 2. Aged ≥ 18 years at the time of informed consent.
• • 3. Life expectancy ≥ 3 months.
• • 4. Have measurable or evaluable disease per RECIST v1.1. The target lesions must not have prior radiation or other locally treated area unless imaging-based progression has been clearly documented following radiation or other local therapy.
• 5. Adequate haematological, liver, and kidney function as follows:
• 1. Bone marrow reserve:
• • • Absolute neutrophil count (ANC) ≥ 1.5 × 109/L without growth factor support in the 2 weeks prior to study entry.
• • • Haemoglobin ≥ 90 g/L without transfusion and/or without growth factor support in 2 weeks prior to study entry.
• • Platelet count ≥ 100 × 109/L without transfusion in 2 weeks prior to study entry.
• 2. Hepatic function:
• • Aspartate aminotransferase (AST), alanine aminotransferase (ALT) \< 3 × upper limit of normal (ULN) (≤5 × ULN if liver metastases or hepatic cell carcinoma (HCC)).
• 3. Renal function:
• • Serum creatinine \< 1.5 × ULN or Serum creatinine clearance (CrCL) \> 50 mL/min, as per the Cockcroft-Gault Equation Glomerular Filtration Rate: \[(140-age in years) × weight in kg\] / (7.2 × serum creatinine in mg/dL) (× 0.85 for females).
• • In PART 2 only: Out of range values for 5a, b and c are allowable based on the discretion of the Investigator and with approval from Sponsor Medical Monitor.
• • 6. International normalized ratio (INR) /prothrombin time (PT) \< 2 x ULN, activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN.
• • In PART 2 only: Out of range values are allowable based on the discretion of the Investigator and with approval from Sponsor Medical Monitor.
• 7. Practice adequate contraceptive measures as per below:
• Female patients must:
• • Be of nonchildbearing potential i.e., surgically sterilised or postmenopausal, or;
• • If of childbearing potential, must have a negative serum pregnancy test at Screening and a negative urine pregnancy test before the first study drug administration and on Day 1 of each Cycle. They must agree not to attempt to become pregnant, must not donate ova, and must agree to use 2 forms of highly effective contraceptive method between signing consent, during the study, and at least 90 days after the last dose of study drug, OR use 1 form of highly effective contraceptive method, plus an additional barrier method of contraception between signing consent, during the study, and at least 90 days after the last dose of study drug.
• • Women of childbearing potential with same sex partners (abstinence from penile vaginal intercourse) are eligible when this is their preferred and usual lifestyle.
• Male patients must:
• • be willing not to donate sperm and if engaging in sexual intercourse with a female partner who could become pregnant, a willingness to use a condom in addition to having the female partner use a highly effective contraceptive method between signing consent, during the study, and at least 90 days after the last dose of the study drug.
• • PART 1 only - Dose Escalation Specific Inclusion Criteria
• • 8. Histologically/cytologically confirmed, locally advanced unresectable or metastatic solid tumours for whom prior treatments have failed, and where an anthracycline may be considered as a treatment option or is indicated. Note that certain malignancies can be included based on imaging (e.g., HCC) based on the discretion of the Investigator with Sponsor Medical Monitor approval.
• • 9. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1
• 10. Adequate Hepatic function as per below:
• * Serum Total bilirubin (TBIL) as per below:
• • 1. Patients with documented Gilbert's syndrome - baseline TBIL \< 3 × ULN,
• • 2. Patient with either HCC or liver metastases - baseline TBIL \< 2 × ULN
• • 3. All other patients baseline TBIL \< 2 × ULN. Exceptions are allowable based on the discretion of the Investigator and with approval from Sponsor Medical Monitor
• • PART 2 only - Exploratory Dose Expansion Specific Inclusion Criteria 8. Histologically/cytologically confirmed solid tumours of any stage for which the patient has not received prior treatment with an anthracycline and for whom treatment with doxorubicin is indicated.
• 9. ECOG performance status ≤ 2 10. Adequate Hepatic function as per below:
• • Serum TBIL as per below:
• • 1. Patients with documented Gilbert's syndrome - baseline TBIL \< 3 × ULN,
• • 2. Patient with either HCC or liver metastases - baseline TBIL \< 3 × ULN
• • 3. All other patients baseline TBIL \< 2 × ULN. Exceptions are allowable based on the discretion of the Investigator and with approval from Sponsor Medical Monitor
• Exclusion Criteria (for Part 1 and Part 2):
• • 1. Females who are pregnant or nursing.
• 2. Received cancer-directed therapy within the following timeframes:
• • 1. Antitumour therapy (chemotherapy, antibody therapy, molecular targeted therapy, hormonal therapy or investigational agent) within 28 days prior to the first dose of study treatment (or 5 times the half-life if shorter than 28 days, there can be exceptions on a case-by-case as approved by Sponsor Medical Monitor based on pharmacology). Note: concurrent use of hormone deprivation therapy for hormone-refractory prostate cancer, bisphosphonate or denosumab for skeletal related events per institution guideline is permitted.
• • 2. Wide-field radiation therapy within 28 days (or palliative radiation therapy within 7 days) prior to the first dose of study treatment or has not recovered from the side effects of radiation therapy in the opinion of the Investigator.
• • 3. Any other concurrent investigational device(s) or conventional agent(s) within 28 days (unless 5 times the half-life is shorter than 28 days) prior to the first dose of study treatment.
• • 4. Therapeutic radiopharmaceuticals must be stopped 8 weeks prior to the first dose of the study drug.
• • 3. Persisting Grade 2 or higher severity AEs from prior antitumour treatment as per CTCAE v5.0. Patients with pre-existing non-treatable Grade 2 toxicities may be eligible per discretion of the Investigator and with approval from Sponsor Medical Monitor (e.g., Grade 2 chemotherapy induced neuropathy).
• • 4. Patients with primary central nervous system (CNS) malignancy, symptomatic CNS metastases, meningeal metastases or leptomeningeal disease are not allowed.
• • Note: Patients with asymptomatic CNS metastases are eligible if clinically controlled, which is defined as 1) ≥ 4 weeks of stable neurologic function following CNS-directed therapy prior to the first dose of study treatment 2) no evidence of CNS disease progression as determined by radiographic imaging ≥ 4 weeks prior to the first dose of study treatment, 3) ≥ 2 weeks from discontinuation of anti-seizure and steroid therapies (receiving prednisone ≤ 10 mg or equivalent steroid therapies is allowed) prior to the first dose of study treatment.
• • 5. Had major surgery within 28-days of the Screening Visit. Note: Patients who have undergone a non-major surgical procedure within 28-days prior to Screening must have recovered adequately from the surgery before the administration of the first dose of study drug. Exception: no waiting period applies following central venous catheter placement.
• • 6. History of tissue or organ transplantation.
• • 7. Treatment with systemic immunosuppressive medications within 4 weeks prior to the first dose of study drug. Exceptions: Daily prednisone equivalent ≤10 mg/day; topical, inhaled, or intranasal corticosteroids.
• • 8. History of severe infection deemed clinically significant by the Investigator or designee within 4 weeks or signs and symptoms of any active infection within 2 weeks prior to the first dose of study treatment.
• • 9. Active hepatitis B or C. Note: Hepatitis B virus (HBV) carriers without active disease (HBV DNA titer \< 1000 copies/mL or 200 IU/mL) or cured hepatitis C (negative HCV RNA test) with confirmed viral clearance that are not receiving ongoing treatment and without residual chronic liver disease may be enrolled.
• • 10. Confirmed human immunodeficiency virus (HIV) infection and receiving anti-retroviral therapy (ART). Patients with well controlled HIV infection (i.e., CD4+ count \>350 cells/μL and viral copies less than 400/mL after at least 4 weeks of ART) may be eligible per discretion of the Investigator and with approval from Sponsor Medical Monitor.
• • 11. Patients with any inherited predisposition to bleeding or to thrombosis (von Willebrand disease, haemophilia, etc.). Patients with a history of nontraumatic haemorrhage (i.e., end stage liver disease, any haemorrhage requiring medical intervention), thromboembolic event or any condition which may increase bleeding risk including clotting disorders, thrombocytopenia during the last 3 months prior to the first dose of study drug administration.
• • 12. Receiving immunosuppressive or myelosuppressive medications that would, in the opinion of the Investigator, increase the risk of serious neutropenic complications.
• • 13. Any other disease or clinically significant abnormality in laboratory parameters, including serious medical or psychiatric illness/condition, which in the judgement of the Investigator might compromise the safety of the patient or integrity of the study, interfere with the patient's participation in the trial or compromise the trial objectives.
• • 14. Known allergies, hypersensitivity, or intolerance to the study drug or its excipients.
• • 15. Any known, documented, or suspected history of illicit substance abuse that would preclude patient from participation, unless clinically justified (i.e., will not interfere with study participation and/or will not compromise trial objectives) per judgement of the Investigator and with approval of Study Medical Monitor. Exception: Physician-prescribed medicinal opioids or cannabinoids are allowed for pain management.
• • 16. Vaccinated with any live vaccine within 4 weeks prior to the first dose of study treatment.
• • 17. Judgement by the Investigator that the patient is unlikely to comply with study procedures, restrictions and requirements.
• • 18. Use of prescription or non-prescription medications, including complementary medicines, within 14 days or 5 half-lives (whichever is longer) if the medication is a potential inhibitor of cytochrome P450 (CYP) isoform 3A4 or 2D6, and/or P-glycoprotein (P-gp), or if the medication is an inducer of CYP3A4 or P-gp, prior to dosing and throughout study participation.
• • PART 1 only - Dose Escalation Specific Criteria
• • 19. Severe or uncontrolled cardiac disease requiring treatment, CHF (New York Heart Association) NYHA III or IV, unstable angina pectoris even if medically controlled, history of myocardial infarction during the 6 months prior to screening, serious arrhythmias requiring medication (with exception of atrial fibrillation or paroxysmal supraventricular tachycardia).
• • 20. Treatment with prior anthracyclines exceeding the maximum equivalent cumulative lifetime dose. In certain cases, patients who have received total cumulative doses may be considered suitable at the discretion of the Investigator in consultation with the patient and the Sponsor Medical Monitor.
• • PART 2 only -Dose Expansion Specific Criteria 19. Uncontrolled or severe cardiac disease that in the opinion of the Investigator would prevent treatment with doxorubicin.