Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Kechow Pharma, Inc.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
1. Written informed consent must be obtained prior to any clinical trial procedures
2. Aged 18 years or over.
3. Must have a pathologically documented solid tumor(s) that has relapsed from, or is refractory to standard treatment, or unable to tolerate toxicities from the SOC/available treatments, or for which no standard treatment is available.
4. Must have at least one measurable lesion as defined by RECISTv1.1 criteria for solid tumors.
5. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
6. Life expectancy ≥3 months (as judged by the Investigator).
7. Must have adequate hematologic function (no blood transfusion and growth factor support for ≥14 days), adequate hepatic and renal function, and some key lab test results meeting the following laboratory values within 7 (+/-2) days before first dosing.
8. Must have the willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures.
11. Known active tuberculosis.
12. Infectious diseases requiring systemic treatment including patients tested positive for COVID-19 according to investigator site/institution's COVID-19 management policies and guidelines.
13. History of allogeneic bone marrow transplantation or organ transplantation.
14. Interstitial lung disease or interstitial pneumonitis, including clinically significant radiation pneumonitis (i.e., affecting activities of daily living or requiring therapeutic intervention). Patients with subclinical pneumonitis who have received immunotherapy previously can be included if his/her condition is stable without any medical intervention.
15. Known hypersensitivity to IP ingredients or their analogues.
16. Unable to swallow IP or has refractory nausea and vomiting, malabsorption, external biliary diversion, or any significant small bowel resection that may interfere with adequate absorption of IP.
17. Concomitant medication which are strong inducers or strong inhibitors of cytochrome P450 CYP2C9, CYP2C19, CYP 3A4.
18. Pregnant or breast-feeding females.
19. Female patients of child-bearing potential or male patients who will not use an effective form of contraception for the duration of the study (until at least 30 days after the last dose of study medication).
You may not be if
1. Have biological, chemotherapy, immunotherapy or radiotherapy less than 4 weeks prior to starting the study treatment.
2. Have undergone or plan to have major surgery (except for tumor biopsy) or experienced severe trauma ≤28 days prior to starting the study treatment.
3. Have active central nervous system lesion (i.e., imaging instability and neurologically unstable). Note: patients who have received stereotactic radiotherapy or surgical treatment for brain tumor can be included after 3 months of procedure without symptoms.
4. Previous or history of second malignancy within 3 years prior to study treatment except for curatively treated.
5. Prior therapy with MEK-inhibitor with severe toxicity causing permanent damage from it, such as ocular, cardiac, pulmonary, etc. disorders and illness.
6. History of any of the following within 6 months prior to Screening:
* Myocardial infarction.
* Unstable angina.
* Coronary artery bypass graft.
* Coronary angioplasty or stenting.
* Chronic heart failure (New York Heart Association Grade ≥2).
* Cerebrovascular accidents including transient ischemic attack, or pulmonary embolism.
* Creatine Phosphokinase (CPK) \>2.5×ULN due to underlying cardiac disorders or myocardial infarction.
7. Mean resting QT calculated using Bazzetts formula (QTcB) ≥480 obtained from three electrocardiograms (ECGs); or family or personal history of long or short QT syndrome; Brugada syndrome or known history of QTc prolongation or Torsade de Pointes within 12 months of Screening.
8. Left ventricular ejection fraction (LVEF) \<50%.
9. History or current evidence of retinal diseases (e.g., retinal vein occlusion \[RVO\] or retinal pigment epithelial detachment, macular degeneration, and retinal detachment).
