2025-523230-77-00招募中2 期
A Phase 2 study of intratumoral administration of L19IL2/L19TNF in locally advanced Basal Cell Carcinoma patients progressed on or intolerant to systemic treatment.
Philogen S.p.A.11 个研究点 分布在 2 个国家目标入组 34 人开始时间: 2026年2月10日最近更新:
适应症
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 34
- 试验地点
- 11
- 主要终点
- Best Overall Response Rate (BORR) as defined by the BCC-RECIST-like criteria according to an Independent Central Review (ICR).
研究概览
简要总结
The primary objective of the study is to evaluate the activity of intratumoral L19IL2/L19TNF in patients locally advanced BCC progressed or intolerant to systemic treatment
入排标准
- 年龄范围
- 18 years 至 65+ years（18-64 Years, 65+ Years）
- 接受健康志愿者
- 否
入选标准
- •Patients must have histologically documented, locally advanced BCC.
- •Male patients with WOCBP partners must agree to use simultaneously two acceptable methods of contraception
- •Patients must have at least one injectable and measurable cutaneous or subcutaneous lesion.
- •Patients must have locally advanced BCC that has progressed on or cannot tolerate standard HHIs and anti-PD1 therapy as assessed by a local multidisciplinary tumor board.
- •Patients with nodal, regional or in transit injectable BCC lesions.
- •Patients must be willing to provide tissue from a core or excisional biopsy of a tumor lesion at screening and for confirmation of Objective Response or Stable Disease.
- •Male or female patients, age 18 - 100 years.
- •ECOG Performance Status/WHO Performance Status ≤
- •Hemoglobin > 10.0 g/dL. Platelets > 100 x 109/L. ALT and AST, GGT and Lipase ≤ 1.5 x the upper limit of normal (ULN).
- •All acute toxic effects (excluding alopecia) of any prior therapy must have resolved to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE v. 5.0) Grade ≤ 1 unless otherwise specified
- •Women of childbearing potential (WOCBP) must have negative pregnancy test results at screening.
排除标准
- •Presence of concomitant malignancies, with the exception of any cancer curatively treated more than 3 years prior to study entry and of tumors with a negligible risk for metastasis or death, such as adequately treated cutaneous squamous cell carcinoma of the skin (surgically removed at least 4 weeks prior to study entry), ductal carcinoma in situ of the breast, or carcinoma in situ of the cervix, early-stage asymptomatic CLL and not under active treatment (Rai 0, Binet A) will be eligible for the study
- •Uncontrolled hypertension. Known uncontrolled coagulopathy or bleeding disorder. Known hepatic cirrhosis or severe pre-existing hepatic impairment. Moderate to severe respiratory failure
- •Active autoimmune disease that has required systemic treatment in past 2 years.
- •Patients have a diagnosis of immunodeficiency or are receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior the first dose of study drug. Limited use of corticosteroids to treat or prevent acute hypersensitivity reactions and asthma/COPD is not considered an exclusion criterion.
- •Known history of allergy to IL2, TNF, or other human proteins/peptides/antibodies
- •Pregnancy or breast-feeding.
- •Ischemic peripheral vascular disease (Grade IIb-IV).
- •Severe diabetic retinopathy.
- •Recovery from major trauma including surgery within 4 weeks prior to enrollment. Solid organ transplant recipient or patient with iatrogenic or pathologic severe immune suppression.
- •Patients with a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the participant's participation for the full duration of the study, or is not in the best interest of the participant to participate, in the opinion of the treating investigator.
- •Patients who have received a live vaccine within 30 days prior to the first dose of study drug. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette–Guérin, and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist®) are live attenuated vaccines and are not allowed.
- •Radiation therapy on the tumor sites in the 4 weeks prior to study drug administration.
- •Any conditions that in the opinion of the investigator could hamper compliance with the study protocol.
- •Current topical or systemic chemotherapy, immunotherapy.
- •Presence of visceral metastasis.
- •Presence of active severe bacterial or viral infections or other severe concurrent disease/infection requiring therapy, including positive tests for human immunodeficiency virus (HIV)-1 or HIV-2 serum antibody, hepatitis B virus (HBV), or hepatitis C virus (HCV). For HBV serology, the determination of HBsAg and anti-HBcAg Ab is required. In patients with serology documenting previous exposure to HBV, negative serum HBV-DNA is required. For HCV, HCV-RNA or HCV antibody test is required. Subjects with a positive test for HCV antibody but no detection of HCV-RNA indicating no current infection are eligible.
- •History within the last year of acute or subacute coronary syndromes including myocardial infarction, unstable or severe stable angina pectoris, inadequately treated cardiac arrhythmias and heart insufficiency (any grade, New York Heart Association (NYHA) criteria).
- •Any abnormalities observed during baseline ECG investigations that are considered clinically significant by the investigator.
- •Known arterial aneurysms.
- •Chronically impaired renal function as indicated by creatinine clearance < 60 mL/min/1.73m2 or for patients older than 65 years without albuminuria or proteinuria, creatinine clearance < 45 mL/min/1.73m2.
结局指标
主要结局
Best Overall Response Rate (BORR) as defined by the BCC-RECIST-like criteria according to an Independent Central Review (ICR).
Best Overall Response Rate (BORR) as defined by the BCC-RECIST-like criteria according to an Independent Central Review (ICR).
次要结局
未报告次要终点
研究者
Lisa Nadal
Scientific
Philogen S.p.A.
研究点 (11)
Loading locations...
相似试验
招募中
2 期
L19IL2/L19TNF in skin cancer patientsPhase II, open label, multicentric, proof-of-principle basket trial in patients with malignant tumors of the skin amenable to intratumoral injection, and in a curative or neoadjuvant or palliative intention, including:
• Basal cell carcinoma (BCC)
• Cutaneous squamous cell carcinoma (cSCC)
• Merkel cell carcinoma (MCC)
• Keratoacanthoma (KA)
• Malignant adnexal tumors of the skin (MATS)
• Tumors from cutaneous T-cell lymphoma (CTCL)
• Kaposi’s sarcoma (KS)2024-518531-10-00Philogen S.p.A.26
尚未招募
2 期
Injection of IP-001 Into Thermally Ablated Hepatic Tumors in Patients With Colorectal Liver MetastasesColorectal Cancer (CRC)Colon Cancer Liver MetastasesRectal Cancer With Liver MetastasesColorectal Liver Metastasis (CRLM)Rectal CancerNCT07321847Immunophotonics, Inc.717
招募中
3 期
Neoadjuvant L19IL2/L19TNF- Pivotal studyMalignant melanoma of the skin in patients with locally advanced and fully resectable melanoma with/without prior therapy and presence of injectable cutaneous and/or subcutaneous or nodal lesions2024-515749-40-00Philogen S.p.A.256
尚未招募
2 期
T Cell Inflamed Gene Expression Profiling Score-guided Anti PD-1 Therapy (Tislelizumab Monotherapy) for Refractory Solid Cancer Patients Unexposed to ImmunotherapyRefractory Solid Cancer Patients Unexposed to ImmunotherapyRefractory Solid Cancer Patients Unexposed to ImmunotherapyNCT07300891Samsung Medical Center72
招募中
2 期
A Phase 3 (Pivotal Stage) Study of NBTXR3 Activated by Investigator’s Choice of Radiotherapy Alone or Radiotherapy in Combination with Cetuximab for platinum-based Chemotherapy-ineligible Elderly Patients with Locally Advanced Head & Neck Squamous Cell CarcinomaLocally Advanced Head & Neck Squamous Cell Carcinoma2024-513082-39-00Nanobiotix60