A Phase 1, Multi-Center, Safety, Dose Escalation, Pharmacokinetics of INV-1120 in Adult Patients Advanced Solid Tumors
Phase 1, first-in-human, open-label dose-escalation study to determine the MTD and RP2D, and to assess the DLT of INV-1120 (also referred to as investigational product or IP). The safety, tolerability, and PK of INV-1120 will be assessed in adult patients with advanced solid tumors.
- Solid Tumor, Adult
- Cancer Metastatic
- Solid Carcinoma
- Solid Tumor, Unspecified, Adult
- Tumor, Solid
- Eligible Ages
- Over 18 Years
- Eligible Genders
- Accepts Healthy Volunteers
- Written informed consent, according to local guidelines, signed and dated by the patient prior to the performance of any study-specific procedures, sampling, or analyses; 2. Patient must be ≥18 years-of-age at the time of signature of the informed consent form (ICF); 3. Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0 or 1; 4. Patients with histologically or cytologically confirmed advanced solid tumors which have progressed on or following standard therapy or for which no standard therapy exists; 5. Patients with life expectancy ≥3 months; 6. Patients with at least one measurable lesion by computed tomography (CT) or magnetic resonance imaging (MRI), according to RECIST v1.1. Tumor lesions that have been irradiated ≥4 weeks before the start of treatment, and have subsequently had documented progression, may be chosen as target lesions in the absence of measurable lesions that have not been irradiated; 7. Patients whose laboratory data at screening meet the acceptable criteria for bone marrow, liver function and renal function. 8. Women of childbearing potential (WOCBP) must have a negative serum pregnancy test (urinary or serum beta human chorionic gonadotropin [β-hCG]) during screening. A woman is considered of childbearing potential (fertile) following menarche and until becoming postmenopausal unless permanently sterile. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause. Postmenopausal women can be included; 9. Male patients with female partners of childbearing potential and female patients of childbearing potential are required to use two forms of acceptable contraception, including one barrier method, during their participation in the study and for 3 months following last dose. Medically acceptable contraception includes: - Hormonal methods (Needs to have been instituted at least 1 month prior to the first dose of study drug): - Barrier methods: - Abstinence, defined as refraining from sexual intercourse 10. Male patients must also refrain from donating sperm from the first dose of study drug until 3 months after the last dose of study drug; 11. Patients must be able to swallow and retain orally administered medication.
- History (≤5 years) or current evidence of cancer that is histologically distinct from the cancer under study, except for cervical carcinoma in situ, superficial non-invasive bladder tumors, or curatively treated Stage I non-melanoma skin cancer; 2. Known serious allergy to investigational drug or excipients (microcrystalline cellulose); 3. History of severe autoimmune disease (including significant ongoing immune-related adverse events of prior immune-oncology therapy) or autoimmune disorder that requires chronic systemic corticosteroid treatment at immunosuppressive doses (prednisone >10 mg/day or equivalent); 4. Known malignant central nervous system disease other than neurologically stable, treated brain metastases - defined as metastases having been treated by surgery, surgery plus radiotherapy or radiotherapy alone, with no evidence of progression or hemorrhage and off any systemic corticosteroids for at least 4 weeks prior to signing the consent; 5. History (within 4 weeks of starting treatment) or evidence of active infections (Grade ≥2); 6. History of seropositive status for human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) at any time before the start of treatment: Testing for seropositive status during screening will be at the discretion of the Investigator in patients without previously reported results; 7. History or evidence of any severe and/or uncontrolled medical conditions or other conditions that, in the opinion of the Investigator and Sponsor, could affect the patient's participation in the study, such as any disorder or surgical procedure that could impact the absorption of study drug from the gastrointestinal tract. 8. History (≤6 months before the start of treatment) or evidence of any of the following: acute myocardial infarction, unstable angina pectoris, coronary artery bypass graft, cerebrovascular accident, or transient ischemic attack; 9. Patients who have impaired cardiac function or clinically significant cardiac diseases, including any of the following: - Congenital long QT syndrome; - Significant ventricular or supraventricular arrhythmias (patients with sinus arrhythmia or chronic rate-controlled atrial fibrillation in the absence of other cardiac abnormalities are eligible); - LVEF < 50% by ECHO or MUGA; - Other clinically significant heart disease such as known congestive heart failure New York Heart Association (NYHA) Class III-IV; 10. Patients with QT interval ≥470 msec in females and ≥450 msec in males at screening using Fridericia's formula (determined as the mean of 3 QTcF values from the screening triplicate ECG obtained with adequate quality); 11. Women who are pregnant or breastfeeding. 12. WOCBP and sexually active fertile men with WOCBP partners who are unwilling or unable to use acceptable contraception method to avoid pregnancy for at least 1 month before the first dose of the study drug, during the study, and for 3 months after the last dose of study drug; 13. Male patient who plans to father a child while enrolled in this study or within 3 months after the last dose of study drug; 14. Not recovered from toxicity from prior anticancer therapy to baseline or Grade 1 (except toxicities which are not clinically significant such as alopecia, skin discoloration). 15. History of an allogeneic bone marrow or solid organ transplant; 16. Use of systemic anti-cancer agent (except luteinizing hormone-releasing hormone (LHRH) agonists, bisphosphonates and denosumab) or investigational drug ≤28 days or five half-lives whichever is longer prior to the first dose of INV-1120; 17. Radiation therapy ≤28 days prior to the first dose of INV-1120, or likely to require radiation therapy at any time until the 30 days after the last dose of INV-1120, except for palliative radiation therapy limited to non-target bone lesions; 18. Major surgery within 4 weeks before enrollment or surgery with ongoing post-operative complications); 19. History of transfusion of platelets ≤2 weeks before the start of treatment; 20. Patients who start erythropoietin or granulocyte-colony stimulating factor (G-CSF), pegfilgrastim, or filgrastim ≤2 weeks before start of treatment; 21. Patients taking medications known to have a significant risk of causing Torsades de Pointes. Patients who have discontinued any of these medications must have a wash-out period of at least 7 days or at least 5 half-lives of the drug (whichever is longer) prior to the first dose of study drug. 22. History of use of H2 blockers (<24 hours before the first dose of INV-1120 and during the study) and proton pump inhibitors (<5 days before the first dose of INV-1120 and during the study). 23. Patients with recent (< 6 months) history, or are currently being treated for gastroesophageal ulcer
- Phase 1
- Study Type
- Intervention Model
- Sequential Assignment
- Primary Purpose
- None (Open Label)
|Subjects will receive escalating doses of INV-1120 orally once a day until un-acceptable toxicity or disease progression. Three to six patients will be enrolled per cohort to evaluate the safety and pharmacokinetics for each dose level. After the last patient in each cohort completes Cycle 1 (DLT observation period of 28 days), the Safety Evaluation Team (SET) will evaluate the safety data and pharmacokinetic collected from Cycle 1, and make the decision whether to escalate the dose before opening the second cohort.||
- Shenzhen Ionova Life Sciences Co., Ltd.
Study ContactMonica Mehta, PhD
1 984 710 8012
Phase 1, open-label dose-escalation study to determine the MTD and RP2D, and to assess the DLT of INV-1120 (also referred to as investigational product or IP). The safety, tolerability, and PK of INV-1120 will be assessed in adult patients with advanced solid tumors. Increasing doses of INV-1120 will be administered to cohorts of 3-6 participants, until the MTD or MAD is reached. The MTD will generally be considered as the RP2D. However, the RP2D may also be determined based on the data of pharmacokinetics, pharmacodynamic biomarkers in blood and the preliminary clinical activity of INV-1120, as well as the incidence rate and nature of the toxicities observed in subsequent cycles beyond Cycle 1. The total number of patients enrolled in the study will depend upon the number of dose-escalation cohorts. It is estimated that approximately 36 evaluable patients will be enrolled in the dose-escalation part of this study. This multicenter study will be conducted in the United States.