Overview

This is a phase 1, open-label, dose escalation and cohort expansion study and conducted in China and the United States to investigate the safety, tolerability and preliminary efficacy of QLH11811 in advanced or metastatic NSCLC patients who have progressed after prior EGFR-TKI treatment. The study consists of the following 2 phases: phase 1: dose escalation (1a) and phase 2: cohort expansion (1b).

Eligibility

Inclusion Criteria:

1. Patients who participate voluntarily, sign informed consent form (ICF), and will be able to follow the study procedures;
2. Aged ≥ 18 years;
3. Patients who are histologically or cytologically diagnosed with EGFR mutation and have unresectable locally advanced or recurrent/metastatic NSCLC;
4. EGFR mutation requirements:

   Dose escalation phase (phase 1a): NSCLC patients who have progressed after standard EGFR-TKI treatment or cannot tolerate standard of care;

   Cohort expansion phase (phase 1b):

   1. Cohort 1: advanced NSCLC patients who have progressed after treatment with third-generation EGFR-TKIs and have EGFR C797S mutation.
   2. Cohort 2: advanced NSCLC patients who have progressed after standard EGFR-TKI treatment but have no other additional driver gene mutation(s).
   3. Cohort 3: advanced NSCLC patients who have progressed after EGFR-TKI treatment and have T790M mutation.
   4. Cohort 4: patients with locally progressed, unresectable or recurrent metastatic NSCLC who are naive to EGFR-TKI treatment and have 19del or 21L858R mutation among EGFR sensitive mutations.
5. Patients who agree to provide tumor samples (fresh tissues or archived samples) for

   analysis of EGFR gene.

   Dose escalation phase: tumor samples collected from the progression site of disease during or after PD after the last TKI treatment should be provided for new genetic testing The subjects who fail to provide tumor samples will be allowed to enroll only after communication and consultation with the sponsor.

   Cohort expansion phase:

   Cohort1: tumor samples collected from the progression site of disease during or after PD after the last TKI treatment should be provided for genetic testing at central laboratory.

   Cohorts 2 and 3: tumor samples collected from the progression site of disease during or after PD after the last TKI treatment should be provided for genetic testing. The genetic testing will be exempted if subjects have the test results meeting the above requirements before their enrollment.

   Cohort 4: tumor samples collected from the progression site of disease during or after PD after the last treatment should be provided for genetic testing (of EGFR mutation); and if subjects are treatment-naive, they will be required to provide the tumor samples only during the screen period. The genetic testing will be exempted if subjects have the test results meeting the above requirements before their enrollment.

6. ECOG ≤ 1 point (for details, refer to Appendix 2 ECOG performance status score);
7. Life expectancy ≥ 12 weeks;
8. Patients who have been diagnosed according to RECIST v1.1 and have measurable lesions as documented by computed tomography (CT) and/or magnetic resonance imaging (MRI) (note: subjects who do not have measurable lesions are allowed to be enrolled in phase 1a study). Note: a measurable lesion for response evaluation has to meet the following criteria: a) it is not in an area that has been involved in prior radiotherapy, or b) there is notable radiographic evidence of progression after the completion of radiotherapy and before study enrollment;
9. Patients who have adequate organ functions and meet the following criteria:
   1. Hematology:

      Absolute neutrophil count ≥ 1.5 × 109/L; platelet count ≥ 100 × 109/L; hemoglobin ≥ 90 g/L (no blood transfusion and no use of granulocyte colony stimulating factor in the 14 days prior to the screening);

   2. Coagulation:

      For patients who have not received anticoagulant therapy: international normalized ratio (INR) of prothrombin time and partial thromboplastin time ≤ 1.5 × ULN;

   3. Liver:

      Alanine aminotransferase (AST) or alanine aminotransferase (ALT) ≤ 3.0 × ULN. For patients with liver metastases: ALT and AST ≤ 5 × ULN, total bilirubin ≤ 1.5 × ULN. For patients with Gilbert syndrome: conjugated bilirubin within normal range;

   4. Kidney:

             Serum creatinine ≤ 1.5 × ULN, or creatinine clearance ≥ 50 mL/min (calculated
             according to Cockcroft-Gault formula, refer to Appendix 4 Creatinine clearance
             calculation formula).
         10. All acute toxic reactions arising from prior antineoplastic therapy or surgery have
             resolved to baseline or reduced in severity to ≤ Grade 1 according to NCI CTCAE V5.0
             (except for alopecia or other toxicities which, in the opinion of the investigator,
             pose no safety risk to the patient);
         11. Patients (both female and male) who agree to take effective contraceptive measures
             from their signing of ICF to 6 months after the last dose of the study drug. For women
             of childbearing potential: negative serum pregnancy test result in 7 days prior to the
             start of treatment is required.
        Exclusion Criteria:
          1. Patients who have received systemic anticancer therapies (e.g., chemotherapy,
             molecularly targeted therapy, radiotherapy, biotherapy, hormone therapy, vaccine
             therapy), or antineoplastic TCM therapy in the 2 weeks prior to the first dose of
             study treatment; or who have received immune-checkpoint inhibitor therapy in the 4
             weeks prior to the first dose of study treatment;
          2. Patients who have received radical radiotherapy (including radiotherapy of more than
             25% of bone marrow) in the 4 weeks prior to the first dose, or who have received local
             palliative radiotherapy for bone metastatic lesions in the 1 week prior to the first
             dose;
          3. Patients who have received strong or moderate CYP3A, P-gp inhibitors in the 1 week
             prior to the first dose or in 5 half-lives of these drugs (whichever is longer), or
             need to continue to receive these drugs during the study; and who have received strong
             or moderate CYP2B6, CYP1A2 and CYP3A inducers in the 4 weeks prior to the first dose;
          4. Patients who are in the treatment period of other interventional clinical studies in
             the 4 weeks prior to the first dose. However, participants of non-interventional
             clinical studies (e.g., epidemiologic studies) are eligible for enrollment in this
             study. Patients in the survival follow-up period of interventional clinical studies
             are also eligible for enrollment in this study;
          5. Patients who have active bacterial, fungal or viral infection requiring systemic
             therapies within the 1 week prior to the first dose;
          6. Patients who have underwent a major operation (e.g., a surgical operation requiring
             local or general anesthesia and hospitalization) in the 3 weeks prior to the start of
             study treatment;
          7. Patients with a history of chronic diarrhea, including but not limited to Crohn's
             disease, irritable bowel syndrome, etc.;
          8. Patients who have experienced > CTCAE Grade 1 continuous diarrhea within the 1 week
             prior to the first dose;
          9. Patients with serious respiratory disorders, e.g. interstitial lung disease, radiation
             pneumonitis, drug-induced pneumonia (however, patients whose conditions have resolved
             and stabilized for 3 months or more are eligible for enrollment);
         10. Patients with symptomatic metastasis to central nervous system (CNS) and/or with
             meningitis carcinomatosa.
             Note: patients with brain metastases whose clinical symptoms have stabilized after
             treatment are eligible for participation in the study, provided that their conditions
             are radiographically stabilized (defined as stability demonstrated by 2 brain images
             acquired by the same imaging technique after treatment of brain metastases). These
             imaging scans should be carried out at an interval of at least 4 weeks, and show no
             signs of intracranial progression. Furthermore, brain metastases or its treatment
             induced neurologic symptoms need to regress to baseline level or resolve. All steroids
             administered as a part of the treatment must be completed ≥ 3 days prior to the
             administration of study treatment.
         11. Patients with clinically significant cardiovascular and cerebrovascular diseases,
             including but not limited to:
               1. Myocardial infarction or unstable angina in the 6 months prior to the first dose;
               2. Stroke or transient ischemic attack in the 6 months prior to the first dose;
               3. Any clinically significant abnormalities in resting ECG in terms of cardiac
                  rhythm, heart rate, conduction or morphology, e.g. complete left bundle branch
                  block, third-degree conduction block, second-degree conduction block, PR interval
                  > 250 ms, etc.;
               4. Uncontrolled hypertension after active treatment: systolic pressure > 180 mmHg or
                  diastolic pressure > 100 mmHg;
               5. Congestive cardiac failure (NYHA functional class III-IV);
               6. Pericarditis or clinically significant pericardial effusion;
               7. Myocarditis;
               8. 12-lead ECG shows that mean QT interval (QTcF) > 450 ms (male) or > 470 ms
                  (female) before the first dose of investigational drug;
               9. Failure to discontinue the drugs that may cause QTc prolongation or torsades de
                  pointes (e.g., antiarrhythmics) during the study.
         12. Patients with clinically uncontrolled serous effusion(e.g., pleural fluid that cannot
             be controlled by drainage or other methods).
         13. Patients with active gastrointestinal disorders or other conditions that have serious
             interference with the drug absorption.
         14. Patients with any condition that have an adverse impact on the swallowing of the drug
             or on the absorption or PK parameters of the investigational drug;
         15. Patients with known serious allergy to the study drug or any excipient of the drug;
         16. Patients with known HIV test positive result and/or treponema pallidum antibody test
             positive result (except for those whose infection has been cured after treatment).
         17. Patients with HBsAg positive result and HBV DNA > 2000 IU/mL or 104 copies/mL (for
             sites which only provide the qualitative testing, HBV DNA test result is positive or
             higher than lower limit of detection); or with HCV antibody positive and HCV RNA
             positive results.
         18. Patients who experienced other malignancies (with the exceptions of Bowen's disease;
             cured basal cell or squamous cell skin cancer; prostate cancer with a Gleason score of
             6; treated cervical carcinoma in situ) in the 2 years prior to the study enrollment.
         19. Pregnant or lactating women. Lactating female subjects need to stop breast-feeding
             before the first dose of study treatment, which cannot be resumed throughout the study
             and in the 6 months after the last dose of study treatment.
         20. Patients with any existing serious or unstable diseases (except for the
             above-mentioned malignancies), psychiatric disorders or any disease or medical
             condition which, in the investigator's opinion, may have an adverse impact on the
             subject safety, the signing of ICF or the compliance with the study procedures.
         21. Patients who are currently participating in a clinical study of other investigational
             therapies.