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New treatment option for MTD
Official title A Clinical Trial to Evaluate Effect of IBD0333 in Patients With Advanced Malignant Tumors
ClinicalTrials.gov ID: NCT06292208
What this study is testing
What is IBD0333?
IBD0333 is an investigational medicine, being studied as a potential treatment for mtd.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- Primary Objectives Dose escalation phase To evaluate the safety and tolerability of IBD0333 in patients with locally advanced/metastatic solid tumor or non-Hodgkin lymphoma and to determine the maximum tolerated dose (MTD), extended recommended dose (DRDE), and/or dose limiting toxicity (DLT). Dose expansion phase To evaluate the safety and tolerability of IBD0333 in patients with locally advanced/metastatic solid tumor or non-Hodgkin lymphoma and to determine the recommended Phase 2 dose (RP2D).
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 80
You may be able to join if
- In order to be eligible for participation in this trial, the patient must:
- Male or female, 18 to 80 years old.
- Patients with histologically or cytologically confirmed locally advanced/metastatic solid tumor or non-Hodgkin lymphoma who have failed or have no...
- There is at least one assessable tumor lesion in the dose escalation phase and at least one measurable lesion in the dose expansion phase according...
- Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Status.
You likely can't join if
- Known hypersensitivity reaction (NCI-CTCAE 5.0 ≥ grade 3) recombinant proteins or any excipient contained in the drug or vehicle formulation for...
- History of 4-1BB monoclonal antibody or 4-1BB-containing dual antibody immune costimulatory molecule agonist.
- History of anti-cancer therapies prior to the initiation of investigational product (chemotherapy within 3 weeks; radiotherapy, biologic therapy...
- Nitrosourea or mitomycin C within 6 weeks prior to the initiation of investigational product;
- Oral fluorouracil and small molecule-targeted drugs within 2 weeks prior to the initiation of investigational product;
- Chinese patent drugs within 2 weeks prior to the initiation of investigational product.
See the full eligibility criteria
Who can join
- In order to be eligible for participation in this trial, the patient must:
- Male or female, 18 to 80 years old.
- Patients with histologically or cytologically confirmed locally advanced/metastatic solid tumor or non-Hodgkin lymphoma who have failed or have no standard therapy, or for whom the standard therapy is intolerant.
- There is at least one assessable tumor lesion in the dose escalation phase and at least one measurable lesion in the dose expansion phase according to RECIST 1.1 (solid tumors) or Lugano 2014 (lymphomas) (tumor lesions...
- Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Status.
- Have a life expectancy of at least 3 months.
- Have adequate organ function as indicated by the following laboratory values.
- Hematological (no transfusion or hematopoietic stimulating factor therapy within 14 days): absolute neutrophil count (ANC)≥1.5×109/L, platelet count (PLT)≥ 90 ×109/L, hemoglobin (HGB)≥90 g/L;
- Hepatic: total bilirubin (TBIL)≤1.5×upper limit of normal (ULN), except for Gilbert syndrome; alanine aminotransferase (ALT) and aspartate aminotransferase (AST)≤3.0×ULN, or ALT and AST ≤ 5.0×ULN in patients with liver...
- Renal: creatinine clearance (Ccr)≥50mL/min (calculated according to the Cockcroft-Gault Method:);
- Coagulation: international normalized ratio (INR) ≤ 1.5×ULN, activated partial thromboplastin time (APTT) ≤1.5×ULN.
- Eligible patients (male and female) of childbearing potential must agree to use a reliable contraception measure (hormonal or barrier contraception or abstinence) with their partner for the duration of the trial and for...
- According to the investigator's assessment, the patient could benefit from IBD0333.
- Patients must have signed an informed consent document stating that they understand the investigational nature of the proposed treatment.
What rules you out
- Known hypersensitivity reaction (NCI-CTCAE 5.0 ≥ grade 3) recombinant proteins or any excipient contained in the drug or vehicle formulation for IBD0333.
- History of 4-1BB monoclonal antibody or 4-1BB-containing dual antibody immune costimulatory molecule agonist.
- History of anti-cancer therapies prior to the initiation of investigational product (chemotherapy within 3 weeks; radiotherapy, biologic therapy, endocrine therapy, targeted therapy, immunotherapy within 4 weeks) and...
- Nitrosourea or mitomycin C within 6 weeks prior to the initiation of investigational product;
- Oral fluorouracil and small molecule-targeted drugs within 2 weeks prior to the initiation of investigational product;
- Chinese patent drugs within 2 weeks prior to the initiation of investigational product.
- History of investigational anti-cancer drug within 4 weeks prior to the initiation of investigational product.
- History of major surgery (except for puncture biopsy) or significant trauma within 4 weeks prior to the initiation of investigational product, or require the selective surgery during the trial.
- History of systemic corticosteroids (prednisone \>10 mg/day or equivalent) or immunosuppressive medication \<14 days prior to the initiation of investigational product. Steroids for topical, ocular, intra-articular...
- Treatment with immunomodulatory agents within 14 days prior to the initiation of investigational product, including but not limited to thymidine, interleukin-2, interferon, etc.
- Vaccination with live attenuated vaccine within 4 weeks prior to the initiation of investigational product.
- History of allogeneic hematopoietic stem cell or organ transplantation.
- The adverse effects related to prior anticancer treatment (except alopecia, peripheral neurotoxicity with grade 2, and stable hypothyroidism after hormone replacement therapy or the other toxicities judged by the...
- Parenchymal brain metastases or meningeal metastases unless previously received therapies and have no evidence of progression on magnetic resonance imaging (MRI) or computed tomography (CT) for at least 8 weeks after...
- Evidence of active infection requiring intravenous systemic therapy.
- History of immunodeficiency, including the positive for human immunodeficiency virus (HIV) antibodies.
- Active hepatitis B infection (HBsAg positive and HBV-DNA \> 500 IU/mL or lower limit of detection [only if lower limit is above 500 IU/mL]). Active hepatitis C is defined by a known positive Hep C Ab result and known...
- Has interstitial lung disease (except for the radiographic pulmonary fibrosis without hormone therapy).
- History of serious cardiovascular disease, including but not limited to:
- Have severe cardiac rhythm or conduction abnormalities, such as ventricular arrhythmias requiring clinical intervention, II-III-degree atrioventricular block, etc.;
- The mean QT interval corrected for heart rate by Fridericia's formula (QTcF) \>470msec.
- History of acute coronary syndromes, congestive heart failure, aortic dissection, stroke or other cardiovascular or cerebrovascular ≥ grade 3 within the 6 months prior to initiation of investigational product.
- Class II, III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system or left ventricular ejection fraction (LVEF) \< 50%, or structural heart disease with high risk...
- Uncontrollable hypertension.
- Previous or current autoimmune disease (systemic lupus erythematosus, rheumatoid arthritis, vasculitis, etc.), except for the stable autoimmune thyroid disease, type I diabetes, vitiligo, cured atopic dermatitis in...
- History of ≥Grade 3 Immune-Related Adverse Events (irAE) or ≥Grade 2 immune-associated myocarditis (experienced immune-associated thyroid toxicity ≥grade 3 could be enrolled).
- History of malignancy or current other malignant tumors (other than in non-melanoma skin cancer, localized prostate cancer, carcinoma in situ [situ cervical cancer] treated with curative intent and without evidence of...
- Has uncontrollable third interstitial fluid that are unsuitable for enrollment (judged by the investigator).
- Has alcohol or drug dependence.
- Has a psychiatric disorder or poor compliance.
- Pregnant or breastfeeding. Have serious systemic disease or are unsuitable for participation in the study.
The study team makes the final eligibility decision.
Where it's taking place
- Jinan, Shandong, China
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 80 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Jinan, Shandong, China. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.