Overview

It is a Phase I/II, Open-label, Multicenter Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of HB0036 in Subjects with Advanced Solid Tumors

Eligibility

Inclusion Criteria

        Patients must meet all the following criteria to be eligible for participation in this
        study:
          1. Male or female. Age ≥ 18 years;
          2. Phase I: Patients with histologically or cytologically confirmed locally advanced,
             recurrent, or metastatic solid tumors (or clinically diagnosed hepatocellular
             carcinoma) that failed all standard therapies known to provide clinical benefit;
             [These solid tumors include but not limit to: non-small cell lung cancer, esophageal
             squamous cell carcinoma, melanoma, head and neck squamous cell carcinomas,
             hepatocellular carcinoma, gastric or gastroesophageal junction adenocarcinoma, renal
             cell carcinoma, etc.];
          3. Phase II: Histologically or cytologically documented locally advanced, recurrent or
             metastatic cancer. There will be several tumor-specific cohorts Advanced non-small
             cell lung cancer cohort Histologically or cytologically documented locally advanced,
             recurrent or metastatic NSCLC; Confirmed availability of representative tumor
             specimens in formalin-fixed paraffin-embedded (FFPE）blocks or at least 5 stained
             serial slides or fresh biopsied specimens (preferred),samples obtained before adjuvant
             / neoadjuvant chemotherapy are allowed only if biopsy cannot be performed; Tumor PD-L1
             expression with a TPS≥1 %; Negative for actionable molecular markers [including but
             not limited to: epidermal growth factor receptor (EGFR) mutations, anaplastic lymphoma
             kinase (ALK) gene fusion mutation, etc.]； Assessed by the investigator as likely to
             benefit from the study drug therapy; and should have progressed at least one prior
             systemic therapy regimen.
             Advanced other cancer cohort Histologically or cytologically documented locally
             advanced, recurrent or metastatic cancer (esophageal squamous cell carcinoma,
             melanoma) Other tumor histologies will be evaluated pending data from the dose
             escalation phase that may inform on possible efficacy in select tumors
          4. At least one measurable lesion( assessable lesion only accepted during accelerated
             titration stage) as per RECIST v. 1.1 defined as non-nodal lesions having at least one
             dimension with a minimum size of 10 mm in the longest diameter by CT or MRI scan or
             ≥15 mm in short axis for nodal lesions. Radiographic disease assessment at baseline
             can be performed up to 21 days prior to the first dose.
             Note: Tumour lesions situated in a previously irradiated area, or in an area subjected
             to other loco-regional therapy, are not considered measurable unless there has been
             demonstrated progression in the lesion.
          5. Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1
          6. Life expectancy ≥12 weeks
          7. Adequate organ function within 14 days of the first dose as defined by the following
             criteria:
             a) Hematology
               -  absolute neutrophil count (ANC) ≥ 1.5×109/L;
                  ② platelets (PLT) ≥ 75×109/L;
                  ③ hemoglobin (HGB) ≥ 90 g/L; Note: The above three items require that patients
                  should not have received any blood component or cell growth factor supportive
                  therapy within two weeks prior to blood sampling.
                  b) Renal function: Calculated creatinine clearance (CrCL) > 50 mL/min
                  (Cockroft-Gault Equation); c) Liver function:
               -  AST and ALT ≤ 2.5×ULN; AST or ALT ≤5×ULN if liver metastases are present;
                  ② Total bilirubin (TBIL) ≤ 1.5×ULN; ≤3 X ULN for patients with Gilbert's disease;
                  d) Coagulation function:
               -  International normalized ratio (INR)or prothrombin time (PT)≤ 1.5×ULN (unless
                  patient on oral anticoagulant with stable dose); ② Activated partial
                  thromboplastin time (APTT)≤ 1.5×ULN;
          8. Women of childbearing potential must confirm a negative serum or urine pregnancy test
             within 3 days prior to the initiation of study treatment; Fertile patients and their
             partners must agree to use effective contraceptives for the duration of study drug use
             and for 90 days after the last administration of study treatment
          9. Recovery to Grade 0-1 from adverse events (AEs) related to prior anticancer therapy
             except alopecia, < Grade 2 sensory neuropathy, and endocrinopathies controlled with
             hormone replacement therapy
         10. The subject is able to understand and willing to sign the ICF; willing and able to
             comply with all study procedures.
        Exclusion Criteria
        Patients are excluded from the study if any of the following criteria apply:
          1. Concurrent malignancy < 5 years prior to entry other than adequately treated cervical
             carcinoma-in-situ, localized squamous cell cancer of the skin, basal cell carcinoma,
             localized prostate cancer, ductal carcinoma in situ of the breast, or < T1 urothelial
             carcinoma. Patients with prostate cancer that is under active surveillance are
             eligible.
          2. Phase I: Patients may have received single agent treatments targeting the TIGIT
             pathway.
             Phase II: Have received previous simultaneous therapy with a PD-1 pathway inhibitor
             and a TIGIT inhibitor; previous monotherapy with TIGIT/PD-1/PD-L1 inhibitor is
             allowed.
          3. Have received antibiotics lasting over 1 week within 28 days prior to first dose;
          4. Have clinically active central nervous system (CNS) metastases and/or carcinomatous
             meningitis. Patients with previously-treated brain or meningeal metastases may
             participate and be eligible for treatment provided they are stable and asymptomatic.
             Patients with asymptomatic brain metastasis or subjects who are symptomatically stable
             after treatment and are on < 10 mg/d prednisone or equivalent are eligible.
          5. Have history of interstitial lung disease or non-infectious pneumonitis (except from
             radiotherapy);
          6. Active autoimmune disease or history of autoimmune disease requiring systemic therapy
             < 2 years prior to screening except hypothyroidism, vitiligo, Grave's disease,
             Hashimoto's disease, or Type I diabetes. Patients with childhood asthma or atopy that
             has not been active in the 2 years prior to study screening are eligible.
          7. History of Grade 3-4 immune-related adverse events (irAEs) or irAEs requiring
             discontinuation of prior therapies, (except for grade 3 endocrinopathy that is managed
             with hormone replacement therapy).
          8. Use of systemic corticosteroids in a dose equivalent to >10 mg/day of prednisone or
             other immunosuppressive agent < 2 weeks prior to screening; the use of topical,
             intraocular, intraarticular, intranasal, or inhaled corticosteroids and systemic
             steroids to prevent (e.g., allergy to contrast agents) or treat non-autoimmune
             condition (e.g., delayed hypersensitivity caused by exposure to allergens) or short
             course (< 5 days) will be allowed
          9. Anticancer therapy or radiation < 5 half-lives or 4 weeks (whichever is shorter) prior
             to study entry; palliative radiotherapy to a single area < 2 weeks prior to study
             screening is permitted. Measurable lesions cannot be previously irradiated unless they
             have demonstrated growth after radiation therapy (RT).
         10. Major surgery (except for diagnostic needle biopsy or intravenous catheterization) or
             chemotherapy/ interventional therapy/radiation therapy/ablation therapy < 4 weeks
             prior to the first dose;
         11. Cerebrovascular accident (CVA), transient ischemic attack (TIA), myocardial infarction
             (MI), unstable angina, or New York Heart Association (NYHA) class III or IV heart
             failure < 6 months of study entry; mean ECG QT-interval corrected according to
             Fridericia's formula (QTcF) > 470 milliseconds (ms) obtained from three ECGs;
             uncontrolled arrhythmia < 3 months of study entry. Patients with rate-controlled
             arrhythmias may be eligible for study entry at discretion of the Investigator.
         12. Patients who have previously received allogeneic stem cell or solid organ
             transplantation.
         13. Have received or will receive a live vaccine within 4 weeks prior to the first dose,
             except COVID-19 vaccine.
         14. Patients whose existing significant clinical abnormalities or laboratory abnormalities
             may affect the evaluation of the study drug by the Investigator's judgement, e.g.
             uncontrolled active infection (>Grade 2, CTCAE v5.0), uncontrolled diabetes, poorly
             controlled hypertension with the combination of the two drugs (systolic blood pressure
             ≥160 mmHg and/or diastolic blood pressure ≥100 mmHg), congestive heart failure,
             myocardial infarction within 24 weeks, etc.;.
         15. Positive results for HIV test.
         16. Active hepatitis B or C. Patients with asymptomatic hepatitis B virus carriers (HBV
             DNA titer < 1000 CPS /mL or 200 IU/mL) or cured hepatitis C (negative HCV RNA test)
             may be enrolled;
         17. Positive COVID-19 qRT-PCR or rapid screening test during screening; can be eligible
             after quarantine (14 days) if COVID-19 test becomes negative.
         18. Patients with active tuberculosis (TB) who are receiving anti-TB treatment or who
             received anti-TB treatment within 1 year prior to screening;
         19. Women who are pregnant or lactating, or women of childbearing potential who do not
             wish to use effective contraception method during the trial.
         20. Men with a partner of childbearing potential who do not consent to use acceptable
             methods of birth control during treatment and for an additional 90 days after the last
             administration of study drug.
         21. History of severe allergic reactions, grade 3-4 allergic reactions to treatment with
             another monoclonal antibody, or known to be allergic to protein drugs or recombinant
             proteins or excipients in HB0036 drug formulation;
         22. Patients who have participated in any clinical trial of a drug or medical device
             within 4 weeks prior to the first dose.
         23. Abuse of alcohol, cannabis- derived products or other drugs; can be eligible with
             remote history of abuse more than 2 years.
         24. Any other serious underlying medical condition (e.g., active gastric ulcer,
             uncontrolled seizures, cerebrovascular incidents, gastrointestinal bleeding, severe
             signs and symptoms of coagulation and clotting disorders, cardiac conditions), or
             psychiatric, psychological, familial condition or geographical location that, in the
             judgment of the Investigator, may interfere with the planned staging, treatment and
             follow-up, affect patient compliance or place the patient at high risk from treatment.
         25. Other conditions which would make it inappropriate for the patient to participate as
             judged by the investigator.