Treatment of advanced malignant tumors with IBC0966

A Phase I/IIa Study to Evaluate the Safety, Tolerability and Efficacy of IBC0966 in Patients With Advanced Malignant Tumors

This study is testing a new treatment called IBC0966 to see if it can help people with advanced cancers that haven't improved with standard treatments.

Quick facts

• Phase: Phase1; Phase2
• Study type: Interventional
• Enrollment: 228 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: SUNHO（China）BioPharmaceutical CO., Ltd. (Industry-sponsored)
• Drugs / interventions: prednisone
• Locations: 1 site (Harbin, Heilongjiang)
• Trial ID: NCT04980690 on ClinicalTrials.gov

What this trial studies

This clinical trial evaluates the safety, tolerability, and efficacy of IBC0966 in patients with advanced malignant tumors. It consists of three phases: a dose escalation phase (Phase Ia), a dose extension phase (Phase Ib), and a clinical exploratory phase (Phase IIa). The trial aims to determine the recommended phase 2 dose (RP2D) and explore the treatment's effectiveness in various types of advanced cancers that have not responded to standard therapies.

Who should consider this trial

Good fit: Ideal candidates include adults aged 18 to 75 with advanced malignant tumors, specifically those with triple-negative breast cancer, non-small cell lung cancer, or head and neck squamous cell carcinoma that have failed standard treatments.

Not a fit: Patients with early-stage tumors or those who have not yet undergone standard treatment may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with advanced malignant tumors who have exhausted standard treatment options.

How similar studies have performed: Other studies have shown promise with similar immunotherapy approaches targeting PD-L1 and CD47, suggesting potential for success in this trial.

Eligibility criteria

Inclusion Criteria:

1. Aged 18 to 75 years old male and female.
2. Phase I (including phase Ia and phase Ib) will enroll patients with advanced malignant tumors who have failed standard treatments.
3. Phase IIa Study-Group A: Recurrent or metastatic triple-negative breast cancer diagnosed by histopathology that has failed standard treatments. Triple-negative breast cancer is defined as estrogen receptor (ER), progesterone receptor (PR), and human epidermis Growth factor receptors (HER2) are all negative.
4. Phase IIa Study-Group B: Advanced/metastatic non-small cell lung cancer with no driver gene mutations that has failed standard treatment confirmed by histopathology.
5. Phase IIa Study-Group C: Recurrent or metastatic head and neck squamous cell carcinoma that failed standard treatments confirmed by histopathology: including nasopharyngeal carcinoma and non-nasopharyngeal head and neck squamous cell carcinoma.
6. Phase IIa study-Group D: Recurrent or metastatic peripheral T-cell lymphoma (PTCL) diagnosed by histopathology that failed standard treatment: Including non-specific PTCL, NK/T-cell lymphoma (nasal type), and angioimmunoblast Cellular T cell lymphoma (AITL), anaplastic large cell lymphoma (ALCL), subcutaneous panniculitis-like T cell lymphoma, enteropathic T cell lymphoma (EATL), and hepatosplenic T cell lymphoma (HSTL) Wait.
7. According to RECIST 1.1 or Lugano 2014 standards, there is at least one measurable lesion, and the measurable lesion has not received local treatment (including local radiotherapy, ablation, and interventional therapy).
8. Agree to provide previously stored tumor tissue specimens or perform a biopsy to collect tumor lesion tissue and send it to the central laboratory for PD-L1 expression level detection and TMB detection.
9. ECOG performance status 0-2.
10. Laboratory examination should meet: ① Blood routine: hemoglobin (HGB) ≥100 g/L, white blood cell count (WBC) ≥3.0×10\^9/L, neutrophil count (ANC) ≥1.5×10\^9/L, platelet count ( PLT) ≥75×10\^9/L; ②Blood biochemistry: total bilirubin (TBIL) ≤1.5×upper limit of normal (ULN), alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3.0×ULN, serum creatinine ( Cr)≤1.5×ULN or calculate the creatinine clearance ≥50 mL/min according to the Cockcroft-Gault formula method.
11. Left ventricular ejection fraction (LVEF) ≥ 50% by echocardiography.
12. Life expectancy ≥3 months.
13. Agree to use at least one medically approved contraceptive method during the trial period and at least 6 months after the last dose (female patients: such as intrauterine devices, contraceptives or condoms, etc.; male patients: such as condoms, abstinence, etc.). Female patients must be non-lactating.
14. Subjects must be fully informed of the content, process and possible risks and benefits of the research and sign the informed consent form. Good compliance, able to complete the study and follow-up.

Exclusion Criteria:

1. Known to have severe hypersensitivity to any monoclonal antibody (≥CTCAE grade 3).
2. Not recovered from the adverse reactions caused by previous anti-tumor treatments (≥CTCAE grade 1), excluding hair loss, pigmentation, and fatigue.
3. Previously received allogeneic hematopoietic stem cell transplantation or solid organ transplantation.
4. Received any live vaccines within 4 weeks before enrollment.
5. Have undergone surgery within 4 weeks before enrollment, and the investigator believes that the patient's state has not recovered to the point where the study can be started.
6. Have a history of hemolytic disease, immune-mediated thrombocytopenia, or Evans syndrome within 3 months before enrollment. Currently suffering from active or suspicious autoimmune disease or a history of autoimmune disease within the past 2 years.
7. Phase Ia and Ib: previous exposure to any CD47 antibody, SIRPα antibody or CD47/SIRPα recombinant protein, or previous exposure to any anti-programmed death receptor 1 (PD-1) or anti-programmed death ligand 1 ( PD-L1) antibody.
8. Received any systemic anti-tumor therapy within 4 weeks before enrollment.
9. Participated in other clinical trials within 4 weeks before enrollment and used clinical investigational drugs during this period.
10. Central nervous system metastases with clinical symptoms were found within 4 weeks before enrollment. Patients who have previously received treatment for brain or meningeal metastases, if clinical stability has been maintained for at least 2 months, and have stopped systemic hormone therapy (dose\>10 mg/day prednisone or other curative hormones) for more than 4 weeks can be included.
11. Patients with ascites (ascites), pleural effusion (pleural effusion) or pericardial effusion that cannot be controlled by drainage or other methods.
12. Past or present suffering from other malignant tumors (except for cured skin basal cell carcinoma and cervical carcinoma in situ).
13. Suffering from serious or poorly controlled diseases, including but not limited to: ① Myocardial infarction, arrhythmia, congestive heart failure, etc. that require treatment or intervention occurred within 3 months before enrollment. ②Human immunodeficiency virus (HIV) infection (HIV antibody positive); hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody (HBcAb) positive and HBV DNA ≥500 IU/mL or ≥1×10\^3 copies/mL) ; HCV antibody positive and HCV RNA positive. ③ Poorly controlled diabetes, hypertension, thyroid disease, etc.; ④Severe and uncontrollable lung diseases (severe infectious pneumonia, interstitial lung disease, etc.) (≥CTCAE grade 3); ⑤Uncontrolled serious Infection (≥CTCAE grade 3).
14. With any situations that the researcher considers inappropriate to participate in this research.

Where this trial is running

Harbin, Heilongjiang

• The Affiliated Tumor Hospital of Harbin Medical University — Harbin, Heilongjiang, China (Recruiting)

Study contacts

• Principal investigator: Qingyuan Zhang — The Affiliated Tumor Hospital of Harbin Medical University
• Study coordinator: tie xu

Conditions Advanced Malignant Tumors; PD-L1; CD47