SIBP-A19 injection for advanced solid tumors

A Phase I Clinical Trial Evaluating the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of SIBP-A19 Injection in the Treatment of Advanced Malignant Solid Tumor Patients

This will test SIBP-A19 injection in adults with advanced solid tumors to find a safe dose and see side effects and how the drug behaves in the body.

Quick facts

• Phase: PHASE1
• Study type: Interventional
• Enrollment: 156 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: Shanghai Institute Of Biological Products (industry)
• Drugs / interventions: chemotherapy, immunotherapy, radiation, prednisone
• Locations: 1 site (Fuzhou, Fujian)
• Trial ID: NCT06990464 on ClinicalTrials.gov

What this trial studies

This open-label, multicenter Phase 1 program uses dose escalation, dose expansion, and indication expansion to study SIBP-A19 given by injection to people with advanced or metastatic solid tumors. An initial 3+3 dose-escalation (if needed) will explore eight planned dose levels (1.0–8.0 mg/kg) to establish the maximum tolerated dose and a recommended Phase 2 dose (RP2D). Selected doses will enter dose-expansion cohorts of 6–9 participants each, followed by indication expansion with at least three cohorts of ~30 participants each at the RP2D. Key outcomes include safety, tolerability, pharmacokinetics, preliminary anti-tumor activity, immunogenicity, QT/QTc effects, and exploratory biomarker analyses.

Who should consider this trial

Good fit: Adults aged 18–75 with histologically or cytologically confirmed advanced or metastatic solid tumors, ECOG 0–1, at least one measurable lesion, adequate organ function, and who have no suitable standard treatment are the intended participants.

Not a fit: Patients with poor performance status, significant organ dysfunction, or those who have effective standard treatment options available are unlikely to benefit from this early-phase trial.

Why it matters

Potential benefit: If successful, SIBP-A19 could become a new treatment option for some patients with advanced solid tumors who have exhausted standard therapies.

How similar studies have performed: Other antibody–drug conjugates (ADCs) have shown clinical activity in certain cancers, but SIBP-A19 itself is being tested in first-in-human early-phase cohorts.

Eligibility criteria

Inclusion Criteria:

* Age range from 18 to 75 years old (including boundary values), regardless of gender.
* Voluntarily participate in this study and sign the informed consent form.
* Participants with advanced or metastatic solid tumors diagnosed by histology or cytology, without standard treatment, standard treatment failure, or intolerance.
* Willing and able to provide sufficient fresh collected or archived tumor tissue samples or provide testing reports from legitimate institutions that meet the requirements.
* There must be at least one measurable lesion as the target lesion.
* ECOG score 0-1.
* Expected survival time ≥ 3 months.
* During the screening period, the main organ functions were basically normal (no medical support such as blood transfusion, granulocyte colony-stimulating factor (G-CSF), or other medical support was received within 14 days before the use of the investigational drug):

  • Blood routine: Absolute value of neutrophils (NE #) ≥ 1.5 × 10 9/L, platelet (PLT) count

  ≥ 90 × 10 9/L, hemoglobin (HGB) ≥ 90 g/L.
* Women of childbearing age during the screening period who have a negative blood pregnancy test and are capable of reproduction (including male participants) have no pregnancy plan and voluntarily take effective contraceptive measures during the trial period and within 6 months after the last dose.

Exclusion Criteria:

* Participants with the following tumors:

  * The participant has had other malignant tumors that have not been cured within the past 5 years (excluding malignant tumors that have been clearly cured, such as thyroid cancer, cured basal cell carcinoma of the skin, and cervical carcinoma in situ).
  * The participant has untreated imaging confirmed central nervous system metastasis.
  * Meningeal metastases.
  * Patients with brain metastases who have received systematic or curative brain metastasis treatment (radiotherapy or surgery) in the past, have been confirmed stable by imaging for at least 4 weeks, and have stopped systemic hormone, antiepileptic, convulsive drugs, and other treatments for more than 2 weeks without clinical symptoms can be enrolled.
* Participants with a history of previous treatment or surgery, or those who received the following anti-tumor treatments during the planned trial period:

  * Patients who accepted the instructions clearly containing traditional Chinese patent medicines and simple preparations with anti-tumor effect within 2 weeks before the first administration;
  * Patients undergoing adjuvant therapy within 6 months after surgery;
  * Patients who have not recovered from the toxicity of the previous anti-tumor treatment to normal or ≤ level 1 (excluding hair loss);
  * Patients who have undergone major surgery, radiation therapy, biological therapy, or chemotherapy within 4 weeks prior to their first administration, or who have received systemic treatment such as unhealed surgical wounds, ulcers or fractures, or other clinical trial drugs.
  * Patients who plan to receive any other anti-tumor treatment (chemotherapy, radiation therapy, immunotherapy, cytokine therapy other than erythropoietin) during the trial period should be excluded (excluding testosterone lowering therapy for prostate cancer patients).
  * The dose (prednisone\>10 mg/d or equivalent) at which immunosuppressive effects are achieved by receiving immunosuppressive agents or systemic corticosteroids within one week prior to the use of the investigational drug.
* Participants with a history of previous illnesses or laboratory tests that show the following abnormalities:

  * Individuals with abnormal coagulation function and a tendency to bleed, or who are undergoing thrombolysis or anticoagulation treatment or have lost blood or donated more than 400 mL within 2 months prior to administration.
  * Have a history of immunodeficiency, including HIV testing positive, or other acquired or congenital immunodeficiency diseases, or a history of organ transplantation.
  * Have a clear history of neurological or psychiatric disorders, including epilepsy or dementia.
  * Known history of drug abuse, alcoholism, or drug use that may affect the results of the trial.
* According to the investigator's judgment, the screening period is accompanied by serious, progressive, or uncontrolled diseases, and the investigator's assessment determines that the participant's participation in the study will increase the risk.
* According to the investigator's judgment, there are serious accompanying diseases that pose a threat to patient safety or affect the completion of the study.
* Patients with uncontrolled ascites, pleural effusion, pericardial effusion during the screening period or those who require drainage, or those who have undergone serosal fluid drainage within 4 weeks before the first administration.
* Patients who must take supplements containing folic acid (such as those with folate deficiency).
* Individuals with a history of severe allergies to protein products, CHO cell products, other recombinant human or humanized antibodies, or components of the investigational drug.
* Pregnant and lactating women.
* Patients who are deemed unsuitable to participate in this clinical study due to other reasons by the investigators.

Where this trial is running

Fuzhou, Fujian

• The Union Hospital affiliated to Fujian Medical University — Fuzhou, Fujian, China (RECRUITING)

Study contacts

• Principal investigator: Ling ying Wu — Chinese Academy of Medical Sciences and Peking Union Medical College
• Study coordinator: Dan dan Chen, Master

Conditions: Advanced Solid Tumors, Advanced solid tumor, ADC, Safety, Efficacy, Pharmacokinetics