Overview
An Open, Multi-Center Phase I/II Clinical Study To Evaluate The Safety, Tolerability, Pharmacokinetic Characteristics And Effectiveness Of HEC169096 In Patients With Thyroid Cancer, Non-Small Cell Lung Cancer, and Other Advanced Solid Tumors.
Description
This is an open-label, multi-center Phase 1/2 study in participants with advanced solid tumors, including RET fusion-positive NSCLC, MTC, and other tumors with RET activation. Phase I of this study includes a dose-escalation phase and a dose-expansion phase , which will focus on exploring MTD and/or RP2D of HEC169096 in patients with advanced solid tumours; Phase II will assess the efficacy and safety of HEC169096 at the RP2D dose.
Eligibility
Inclusion Criteria:
- Phase 1：Pathologically documented, definitively diagnosed non-resectable advanced solid tumor.
- Phase 2： All participants must have an oncogenic RET-rearrangement/fusion or mutation (excluding synonymous, frameshift, and nonsense mutations) solid tumor.
- Participants has Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-2.
- Measurable or non-measurable disease as determined by RECIST 1.1;
- Adequate hematologic, hepatic and renal function;
- Life expectancy of at least 12 weeks;
- Negative pregnancy test (urine or serum) for female patients of childbearing potential;
- Participants agrees to provide tumor tissue (archived, if available or a fresh biopsy).
Exclusion Criteria:
- Participant's cancer has a known primary driver alteration other than RET.
- Nitrosourea, anthracyclines and mitomycin chemotherapy within 6 weeks prior to study treatment;
- Chemotherapy, immunotherapy, radiotherapy, or major surgery within 4 weeks or 5 half-lives (whichever is longer) prior to study treatment;
- Those who have received more than 30% of bone marrow radiation or wide-range radiotherapy within 4 weeks before the first study drug treatment (the patients receiving palliative radiotherapy are within 2 weeks before receiving study drug treatment);
- Had received traditional Chinese medicine for anti-tumor within a week before receiving study drug treatment;
- Had received live vaccine within 4 weeks prior to study treatment;
- Had received any investigational agent from other clinical study within 4 weeks or 5 half-lives (whichever is longer) prior to study treatment or are currently participating in other clinical trials;
- Any unresolved toxicities from prior therapy greater than Common Terminology Criteria for Adverse Events (CTCAE) Grade 1 at the time of starting study treatment .
- Central nervous system (CNS) metastases or a primary CNS tumor that is associated with progressive neurological symptoms.
- Patients with other malignant tumors within 5 years before the first use of drugs
- Patients have a history of severe cardiovascular disease;
- Active hepatitis (Hepatitis B: HBsAg-positive and HBV-DNA ≥ 2000 IU/ mL or ≥ 10^4 cps/ mL; Hepatitis B: HCV antibody-positive and HCV-RNA positive), HIV antibody-positive.
- Patients with clinically active interstitial lung disease, active pneumonia, and radiation pneumonia requiring treatment;
- Poorly controlled pleural effusion, abdominal effusion, or pericardial effusion after intervention (such as drainage);
- Clinically significant active malabsorption syndrome or other diseases that may affect study drug administration and gastrointestinal absorption;
- Patients have been treated with any strong CYP3A inhibitors or inducers within 2 weeks prior to the first dose or PPIs in the first week before the first dose.