Investigating ILB-3101 for patients with advanced solid tumors

Phase I/II Study of the ILB-3101 in Patients with Advanced Solid Tumors

This study is testing a new treatment called ILB-3101 for people with advanced solid tumors to see if it is safe and helps fight their cancer after other treatments have not worked.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 240 (estimated)
• Ages: 18 Years to 80 Years
• Sex: All
• Sponsor: Innolake Biopharm (Industry-sponsored)
• Drugs / interventions: chemotherapy, immunotherapy, radiation, prednisone
• Locations: 1 site (Shanghai)
• Trial ID: NCT06426680 on ClinicalTrials.gov

What this trial studies

This clinical trial evaluates ILB-3101, a humanized antibody-drug conjugate targeting B7-H3, in patients with advanced solid tumors. It is an open-label, multi-center, phase 1 study conducted in China, consisting of a dose escalation phase followed by a dose expansion phase. The study aims to assess the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity of ILB-3101 in participants who have progressed on or are intolerant to standard therapies. Participants will be monitored for adverse events throughout the treatment and for 28 days post-treatment.

Who should consider this trial

Good fit: Ideal candidates include adults aged 18-80 with advanced solid tumors that are refractory to standard treatments or for whom no standard treatment is available.

Not a fit: Patients with early-stage tumors or those who have not yet received standard therapies 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 solid tumors who have limited treatment choices.

How similar studies have performed: Other studies using antibody-drug conjugates have shown promising results, indicating potential success for this novel approach.

Eligibility criteria

Inclusion Criteria:

1. Have signed informed consent forms voluntarily.
2. 18-80 years old.
3. Having an ECOG performance status score of 0 or 1.
4. With an expected survival of more than 12 weeks.
5. Diagnosed histologically or cytologically with local advanced or metastatic solid cancer, and under one of following situations: standard treatment-refractory (disease progression or no response), treatment-resistant, unable to receive treatment, or the standard treatment is unavailable.
6. Need to provide archived tumor tissue samples (Formalin fixed or paraffin embedded tissue blocks or at least 5 unstained sections); During the dose escalation stage, for subjects who are unable to provide tumor samples or have insufficient samples, the decision to enroll may be made based on specific circumstances after discussion with the sponsor.
7. At least one assessable tumor lesion is present during the dose escalation phase, and according to RECIST version 1.1, at least one measurable tumor lesion is present during the dose escalation phase (CRPC can be determined based on PCWG3).
8. Having sufficient bone marrow, liver, and kidney functions (based on the normal value of the clinical trial site):

   1. Absolute neutrophil count (ANC) ≥ 1.5×109/L.
   2. Platelets ≥ 75×109/L.
   3. Hemoglobin ≥ 90g/L.
   4. Total serum bilirubin ≤ 1.5×upper limit of normal (ULN).
   5. Without liver metastases, ALT, AST ≤ 2.5×ULN; with liver metastases, ALT, AST ≤ 5×ULN.
   6. Serum creatinine ≤1.5 × ULN.
   7. Creatinine clearance rate (CrCl) (creatinine only ˃ Calculation required for 1.5 × ULN ≥50 mL/min (Calculate according to Cockcroft Fault formula),
   8. International Normalized Ratio (INR) ≤ 1.5×ULN, APTT ≤ 1.5×ULN.
   9. Echocardiographic LVEF (left ventricular ejection fraction) ≥ 50%.
   10. QT interval corrected by Fridericia method (QTcF) Male\<450ms; Female\<470ms.
9. The serum pregnancy test results of female subjects of childbearing age are negative.
10. Male or female patients of childbearing potential must agree to use effective methods of contraception (such as double-barrier contraceptive methods, condoms, oral or injectable contraceptives and intrauterine devices) during the study period and within 90 days after the last dosing.

Exclusion Criteria:

1. Within 3 weeks prior to the first administration, systemic anti-tumor therapy has been received, including chemotherapy, curative radiotherapy (palliative radiotherapy for a single lesion within 3 weeks prior to enrollment is allowed, and radiotherapy is not allowed for measurable lesions before enrollment unless it is confirmed that the lesion has progressed after radiotherapy), biological therapy, immunotherapy, etc., except for the following:

   1. Received urea nitrite or mitomycin C within 6 weeks prior to the first use of the study drug.
   2. Oral administration of fluorouracil or small molecule targeted drugs within 2 weeks prior to the first use of the investigational drug or within 5 half-lives of the drug (whichever is longer).
   3. Individuals who have received endocrine therapy within 2 weeks prior to the first use of the investigational drug.
   4. Traditional Chinese patent medicines and simple preparations or traditional Chinese medicine with anti-tumor indication within 1 week before the first use of the study drug.
2. Patients who received other clinical trial drug within 4 weeks before the first dosing.
3. Within 3 years prior to the first trial drug treatment, the patient had other active malignant tumors, except for the tumors participating in this study and other locally cured tumors (such as basal skin cancer, papillary thyroid cancer, or any type of in situ cancer that has been completely removed, such as cervical in situ cancer, ductal carcinoma in situ, etc.).
4. The presence of clinically uncontrollable pleural/abdominal effusion, pericardial effusion, determined by the investigators as unsuitable for inclusion.
5. Suffering from central nervous system metastasis and/or cancerous meningitis. Except for asymptomatic or asymptomatic central nervous system metastases that have been clinically controlled but are judged stable by investigators, the following conditions must also be met:

   1. Stable clinical symptoms for at least 4 weeks before receiving trial drug treatment.
   2. No evidence of central nervous system disease progression was found in imaging examinations within 4 weeks prior to the first trial drug treatment.
   3. Antiepileptic drugs have been discontinued at least 2 weeks prior to the first trial drug treatment, and the dosage of prednisone is ≤ 10mg/day or equivalent dose of steroids.
   4. For patients with intracranial lesions, if they have received treatment (such as radiotherapy) before the first trial drug treatment, elution should be ≥ 2 weeks. Cancer induced encephalitis should be excluded regardless of its stable clinical condition.
6. Receiving drug therapy known to prolong the QT interval or potentially lead to torsade de pointe ventricular tachycardia; Or continue to receive these medications during the research period.
7. Acute coronary syndrome occurring within the past 6 months, including myocardial infarction, unstable angina, symptomatic congestive heart failure (New York Heart Association classification II-IV), aortic dissection, stroke, or other grade 3 or higher cardiovascular and cerebrovascular events; Serious cardiac rhythm or conduction abnormalities, such as ventricular arrhythmias requiring clinical intervention, II-III-degree atrioventricular block, etc.
8. Suffering from clinically uncontrollable diseases, including but not limited to severe diabetes (diabetes ketoacidosis or hyperglycemia hyperosmolality occurred within 6 months before the first administration, and the detection value of glycosylated hemoglobin in the screening period was ≥ 7.5%); Refractory hypertension (systolic blood pressure ≥ 150mmHg or diastolic blood pressure ≥ 100mmHg after optimal medical treatment within the first month of screening) or a history of hypertensive crisis or hypertensive encephalopathy.
9. Individuals with previous or current interstitial lung disease (excluding radiation pneumonia that does not require hormone therapy).
10. Evidence of persistent uncontrolled systemic bacterial, fungal, or viral infections (including HIV infection, HIV antibody positive; syphilis infected individuals) and current need for intravenous anti infection treatment.
11. Provisions on hepatitis B and hepatitis C: if hepatitis B surface antigen (HBsAg) is positive, and HBV-DNA\>2000 IU/ml or 104 copies/ml, hepatitis B virus infected persons should receive antiviral treatment according to local guidelines and standards and are willing to receive antiviral treatment throughout the study period; Hepatitis C antibody positive, and HCV RNA higher than the upper limit of normal values in the study site;
12. Within 14 days prior to the first administration, systemic corticosteroids (prednisone\>10mg/day or equivalent doses of similar drugs) or other immunosuppressive treatments have been received, except for the following:

    1. Use local, ocular, intra-articular, intranasal, and inhaled corticosteroids for treatment.
    2. short term use of glucocorticoids for preventive treatment (such as preventing contrast agent allergies).
13. Within 4 weeks before the first administration or planned to receive attenuated live vaccines during the study period.
14. Having undergone major organ surgery (excluding biopsy) or significant trauma within 4 weeks prior to the first administration or requiring elective surgery during the trial period.
15. Individuals who have received allogeneic hematopoietic stem cell transplantation or organ transplantation in the past.
16. Known to have alcohol or drug dependence.
17. Individuals with mental disorders or poor compliance.
18. The adverse reactions of previous anti-tumor treatments have not yet recovered to CTCAE5.0 ≤ Grade 1 (excluding toxicity judged by the investigators to have no safety risk, such as hair loss, grade 2 peripheral neurotoxicity, stable hypothyroidism after hormone replacement therapy, etc.);
19. Known to cause clinically significant allergic reactions to the active ingredients and excipients, antibodies, and other monoclonal antibodies.
20. Pregnant (positive pregnancy test prior to dosing) or breast-feeding women.
21. The investigators believe that the subjects are not suitable to participate in this clinical study due to other reasons.

Where this trial is running

Shanghai

• Fundan University Shanghai Cancer Center — Shanghai, China (Recruiting)

Study contacts

• Principal investigator: Jian Zhang, MD — Fudan University
• Study coordinator: Yan Li, MD

Conditions Advanced Solid Tumor