Testing IBR854 for advanced solid tumors

A Phase I Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of IBR854 Cell Injection in Patients With Unresectable Locally Advanced Or Metastatic Solid Tumors

This study is testing a new treatment called IBR854 to see if it can safely help people with advanced solid tumors that can't be removed by surgery.

Quick facts

• Phase: PHASE1
• Study type: Interventional
• Enrollment: 18 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: Imbioray (Hangzhou) Biomedicine Co., Ltd. (industry)
• Drugs / interventions: chemotherapy, immunotherapy, prednisone
• Locations: 1 site (Beijing, Beijing)
• Trial ID: NCT06001684 on ClinicalTrials.gov

What this trial studies

This open-label, phase I study aims to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of IBR854 cell injections in patients with unresectable, locally advanced, or metastatic solid tumors. The study follows a dose escalation design, administering doses of 3.0×10^9, 5.0×10^9, and 7.0×10^9 cells on specific days within a 21-day cycle. Enrollment occurs in groups of 3-6 subjects, with careful monitoring for dose-limiting toxicities before advancing to higher doses.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18-75 with unresectable, locally advanced, or metastatic solid tumors and an ECOG score of 2 or less.

Not a fit: Patients with resectable tumors or those who have access to standard care options 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 currently have no standard care.

How similar studies have performed: While this approach is novel, similar studies targeting advanced solid tumors have shown promise in the past.

Eligibility criteria

Inclusion Criteria:

1. Subjects volunteer to participate in this clinical study, are fully aware of the study and have signed the Informed Consent Form (ICF). Subjects are willing to follow and able to complete all trial procedures.
2. Age: adult at the age of 18-75 (both inclusive), female or male.
3. Subjects with histologically or cytologically confirmed, unresectable, locally advanced or metastatic solid tumors (which can be diagnosed with the use of tumor markers in combination with imaging for specific advanced tumors, such as liver cancer) who have no current standard of care.
4. Eastern Cooperative Oncology Group (ECOG) score ≤2 and expected survival time \>3 months.
5. According to the Response Evaluation Criteria in Solid Tumors (RECIST) V1.1 criteria, the subjects have at least one target lesion (non-lymph node lesion with major diameter ≥ 1.0cm or lymph node lesion with minor diameter ≥ 1.5 cm). A lesion that is within the field of previous radiotherapy could not be considered a target unless there is radiographic evidence of progression.
6. Organ function during screening should meet the following criteria:

   * Absolute neutrophil count (ANC) ≥1.5×10\^9/L; Platelet (PLT) ≥75×10\^9/L; Hemoglobin (Hb)≥80g/L (no blood transfusion or hematopoietic stimulator treatment within 7 days).
   * Alanine aminotransferase (ALT)≤3×ULN (Patients with liver metastasis: ≤5×ULN); Aspartate aminotransferase (AST)≤3×ULN (Patients with liver metastasis: ≤5×ULN);
   * Creatinine (Cr) ≤2× ULN; Creatinine clearance (Ccr) (to be calculated only when Cr \> 2× ULN) \> 50ml/min (Cockcroft-Gault formula);
   * Activated partial thrombin time (APTT) ≤1.5×ULN, International normalized ratio (INR) ≤1.5×ULN (Patients with anticoagulants: ≤ 2.5×ULN).
7. Subjects of reproductive age and their partners should agree to have no family planning and to use effective contraceptive methods for 6 months from signing the ICF until the last dose of the study drug is administered.

Exclusion Criteria:

1. Have received systemic antitumor therapy within 4 weeks or five half-lives of the drug (whichever is longer) before the first dose of the study drug: Systemic chemotherapy (2 weeks for oral fluorouracil, 6 weeks for mitomycin C and nitrosoureas), endocrine therapy, targeted therapy (2 weeks or 5 half-life for small molecule targeted therapy, whichever is longer), immunotherapy, radical radiotherapy, tumor embolization, Chinese herbal medicine for anti-tumor indications, etc. Or received palliative radiotherapy within 2 weeks before the first dose.
2. Toxic effects from previous antitumor therapy have not returned to grade 1 or less (other than alopecia or fatigue).
3. Any prior adoptive cellular immunotherapy.
4. Active brain metastases (one of the following criteria: clinical symptoms; A new diagnosis; Progression after previous local treatment).
5. Have undergone major organ surgery within 4 weeks prior to their first use of the study drug, or required elective surgery during the study period.
6. Long-term (≥ 3 days) treatment with a glucocorticoid (prednisone \> 10 mg per day or equivalent) or another immunosuppressive agent is anticipated to be required during the study. Inhaled or topical steroid hormones are allowed in subjects without active autoimmune disease
7. Have received a live or attenuated vaccine within 4 weeks before the first dose or plan to receive a live or attenuated vaccine during the study period.
8. Have severe infections that cannot be controlled.
9. Active hepatitis B, hepatitis C virus infection or HIV infection.
10. Have undergone an allogeneic bone marrow transplant or other organ transplant.
11. Have active autoimmune diseases or have had autoimmune diseases that are likely to recur (e.g., systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, autoimmune thyroid disease, vasculitis, psoriasis, etc.). Except in the following cases: type 1 diabetes that was well controlled with hormone replacement therapy, hypothyroidism, skin conditions that did not require systemic therapy (e.g., vitiligo), and other conditions that were well controlled and that the investigator determined were less likely to recur (e.g., childhood asthma in remission).
12. Have a history of serious cardiovascular and cerebrovascular diseases, including but not limited to:

    * There are serious cardiac rhythm or conduction abnormalities, such as ventricular arrhythmia, and Ⅱ-Ⅲ degree atrioventricular block, which need clinical intervention;
    * Prolonged QT interval corrected with Fridericia's method (QTcF) (\>450 ms in men; \>470 ms for women)
    * Acute coronary syndrome, congestive heart failure, aortic dissection, stroke, or other grade 3 or above cardiovascular and cerebrovascular events occurring within 6 months before the first administration;
    * Patients with heart failure or left ventricular ejection fraction (LVEF) \< 50% in the New York Heart Association (NYHA) classification ≥II;
    * Hypertension beyond clinical control.
13. Clinically significant chronic obstructive pulmonary disease or other moderate to severe chronic respiratory disease developed within 6 months.
14. Have other malignant tumors in the past 3 years, excluding skin basal cell carcinoma, ductal carcinoma in situ and cervical carcinoma in situ with a radical surgery.
15. Pregnant or lactating women.
16. Have mental disorders or a history of alcohol, drug or drug abuse within one year.
17. Have participated in other clinical trials and received any unmarketed investigational drug or treatment within 4 weeks prior to first use of the study drug.
18. Allergic to the main components of the study drug.
19. The investigator considered that the subjects had a history of other serious systemic diseases or other reasons that made them unsuitable for the study.
20. Unsuitable for participation in this study considered by the investigators.

Where this trial is running

Beijing, Beijing

• Cancer Institute and Hospital, Chinese Academy of Medical Sciences — Beijing, Beijing, China (RECRUITING)

Study contacts

• Principal investigator: Ning Li, MD, PhD — Cancer Institute and Hospital, Chinese Academy of Medical Sciences
• Study coordinator: Ning Li, MD, PhD

Conditions: Solid Tumors