Overview

A single-center, open-label dose-escalation design to evaluate the safety and efficacy of KN5001 in patients with pulmonary nodules.

Eligibility

Inclusion Criteria:

1. Subjects voluntarily sign the informed consent form, understand this clinical study, and are willing to follow and able to complete all trial procedures;
2. 18-70 years old, male or female;
3. Subjects with lung nodules confirmed by imaging examination must meet the following

   conditions

     Multiple high-risk nodules have been surgically removed and confirmed to be
     malignant lesions, and the remaining high-risk nodules (refer to the standards in
     Appendix 12) cannot be surgically removed again, and are not suitable for other
     effective treatments or have failed other treatments;

4. If the subject is unable to complete the puncture or the puncture fails, the subject

must be diagnosed as a malignant nodule through PET-CT imaging examination.

Exclusion Criteria:

1. Subjects who are known to have allergic reactions, hypersensitivity reactions, intolerances or contraindications to any component of KN5001, or subjects with a history of severe allergic reactions;
2. Subjects with the following genetic syndromes: Fanconi syndrome, Kostmann syndrome, Shwachman syndrome or any known bone marrow failure syndrome;
3. Subjects with active or uncontrolled infections requiring parenteral antibiotics; Evidence of a serious active viral or bacterial infection or an uncontrolled systemic fungal infection;
4. Subjects with heart failure of grade III or IV according to the New York Heart Association (NYHA) cardiac function classification standard (see Appendix 1);
5. Subjects with a history of epilepsy or other central nervous system diseases;
6. Subjects with a history of malignant tumors, excluding patients with cured skin or cervical carcinoma in situ and patients with inactive tumors;
7. Subjects with a significant bleeding tendency, such as gastrointestinal bleeding, coagulopathy, hypersplenism, etc.;
8. Subjects with unstable angina, symptomatic congestive heart failure, or myocardial infarction in the past 6 months;
9. Females who are pregnant, lactating, or planning a pregnancy within six months;
10. Subjects who have received other clinical trial treatment within 3 months;
11. Any situation judged by the investigators that may increase the risk of the subjects or interfere with the clinical trial outcome.