A Study of KC1036 in Patients with Advanced Thymic Tumors

Launched by BEIJING KONRUNS PHARMACEUTICAL CO., LTD. · Jan 5, 2023

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment called KC1036 for patients with advanced thymic tumors, specifically recurrent thymoma or thymic carcinoma that cannot be removed with surgery. The goal is to see how effective and safe this treatment is for people who have already tried other therapies without success. The trial is currently looking for participants who are between 18 and 80 years old and have been diagnosed with these types of tumors. To qualify, patients should have measurable tumors, good overall health with a life expectancy of at least 12 weeks, and must be willing to sign consent to participate.

If you join the trial, you will receive KC1036, and your progress will be closely monitored throughout the study. It's important to know that certain health conditions or previous treatments may disqualify you from participating. For example, individuals with other active cancers, autoimmune diseases, or certain infections are not eligible. This trial provides an opportunity to access a potentially new treatment while contributing to research that could help others in the future. If you’re interested, talk to your doctor for more information about your eligibility and what participating would involve.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Patients with thymoma or thymic carcinoma confirmed by cytologically or histologically (WHO Classification of Thoracic Tumors 5th ed), including all pathological subtypes;
• • Patients with advanced recurrent, unresectable and/or metastatic thymic tumor as defined by the Masaoka-Koga stage;
• • Subsequent relapse of disease following first-line systemic chemotherapy;
• • Patients with at least one measurable lesion as defined by RECIST V1.1; Measurable lesions located within the radiation field of previous radiotherapy or after local treatment can also be selected as target lesions if progression is confirmed.
• • Eastern Cooperative Oncology Group performance status score of 0 or 1;
• • Life expectancy \> 12 weeks;
• • Adequate organ and marrow function;
• • Patients should participate in the study voluntarily and sign informed consent.
• Exclusion Criteria:
• • Patients with thymus neuroendocrine tumors;
• • Any patient who is known to have central nervous system (CNS) metastasis or imaging shows a risk of CNS metastasis;
• • Previous (within the last 5 years) or current malignancies at other sites;
• • Gastrointestinal abnormalities;
• • Cardiovascular and cerebrovascular diseases;
• • Patients who have previous treatment with small molecule VEGFR-TKI (except patients whose treatment cycle is less than 2 weeks due to intolerance or other reasons); Patients who have previous treatment with PD-1 / PD-L1 antibody combined with small molecule VEGFR-TKI;
• • Involved in other clinical trials within 4 weeks before enrollment; Prior anti-tumor therapies with chemotherapy, cytotherapy, immunotherapy, operation (Interventional therapy excepted) within 4 weeks 4 weeks before enrollment; Prior radiotherapy (palliative radiotherapy excepted) within 2 weeks; Prior small-molecule targeted therapy within 2 weeks or 5 half-lives.
• • Presence of unresolved toxicities from prior anti-tumor therapy, defined as having not resolved to NCI CTCAE V5.0 grade 0 or 1 with the exception of alopecia;
• • Skin wound, surgical site, wound site, mucous membrane severe ulcer or fracture comfirmed as having not recovered;
• • Uncontrolled mass pleural effusion, ascites, and pericardial effusion;
• • Active autoimmune diseases: Myasthenia gravis, pure red cell aplastic anemia, systemic lupus erythematosus, inflammatory bowel disease, etc;
• • Need immunosuppressive agents or hormone therapy for immunosuppression, , and still need immunosuppressive therapy within 2 weeks before enrollment;
• • Active bacterial, viral or fungal infection; Fever of unknown cause (\> 38.5℃) occurred within 2 weeks before enrollment;
• • Patients who are positive for both Hepatitis B surface antigen (HBsAg) and hepatitis B virus deoxyribonucleic acid (HBV-DNA) quantification results; Patients who are positive for both hepatitis C virus antibody (HCAB) and hepatitis C virusribonucleic acid (HCV-RNA) quantification results; Patients who are positive for human immunodeficiency virus (HIV);
• • Pregnant or lactating women;
• • Patients who do not take contraception during the study period and within 6 months after the study;
• • Patients with insufficient compliance as evaluated by investigator;
• • The investigator believes that it is not suitable to patient in this clinical trial.