A Phase I Study to Evaluate the Safety and Dosimetry of 68Ga-labelled OncoFAP Derivatives in Patients with Solid Tumors
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 18
- 试验地点
- 5
- 主要终点
- Safety (AE)
研究概览
简要总结
The primary objectives of this trial are to evaluate the safety and dosimetry of [68Ga]Ga-OncoFAP for detection/imaging of solid tumors.
详细描述
Phase I, multicenter study in patients with a confirmed diagnosis of solid tumor among breast cancer, colorectal cancer, oesophageal cancer and pancreatic adenocarcinoma, requiring clinical staging for nodal staging and/or metastatic disease (based on institutional practice and risk stratification). All patients will receive a single intravenous bolus administration of 250 MBq (225 - 275 MBq). [68Ga]Ga-OncoFAP biodistribution, PK, and dosimetry of [68Ga]Ga-OncoFAP will be assessed based on a series of PET/CT scans, blood and urine sampling.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with a confirmed diagnosis of breast cancer, colorectal cancer, oesophageal cancer and pancreatic adenocarcinoma. Confirmation by histopathology is required for breast, colorectal and oesophageal cancer. For pancreatic adenocarcinoma, confirmation by histopathology or cytology obtained by endoscopic ultrasound is accepted.
- •Requirement for diagnostic imaging or imaging performed within 4 weeks prior to the [68Ga]Ga-OncoFAP-PET/CT scan for staging.
- •Male or non-pregnant and non-breastfeeding female.
- •For female patients: negative serum pregnancy test for women of childbearing potential* (WOCBP).
- •WOCBP must agree to use, from the screening to six months following the study drug administration, highly effective contraception methods, as defined by the "Recommendations for contraception and pregnancy testing in clinical trials" issued by the Head of Medicine Agencies' Clinical Trial Facilitation Group (www.hma.eu/ctfg.html) and which include, for instance, progesterone-only or combined (estrogen- and progesterone-containing) hormonal contraception associated with inhibition of ovulation, intrauterine devices, intrauterine hormone-releasing systems, bilateral tubal occlusion or vasectomized partner.
- •For male patients: male subject able to father children must agree to practice effective contraception for three months starting from the study drug administration.
- •Age 18 - 75
- •Patient must not have any concomitant infections or active concomitant disease.
- •Life expectancy of more than 12 weeks.
- •Ability to undergo imaging study procedures.
- •Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
- •Willingness and ability to comply with the scheduled visits, plan, laboratory tests and other study procedures.
- •Women of childbearing potential are defined as females who have experienced menarche, are not postmenopausal (12 months with no menses without an alternative medical cause) and are not permanently sterilized (e.g., tubal occlusion, hysterectomy, bilateral oophorectomy, or bilateral salpingectomy).
排除标准
- •Chronically impaired renal function as expressed by creatinine clearance < 60 mL/min or serum creatinine > 1.5 x ULN.
- •Presence of active hepatitis.
- •Presence of significant cardiac disorders (congestive heart failure, NYHA class III-IV, myocardial infarction within one year prior to study entry, uncontrolled hypertension, or arrhythmia).
- •Pregnant or breastfeeding during participation in the study.
- •Any concomitant condition which in the opinion of investigators makes it undesirable for the patient to participate in the study or which could jeopardize compliance with the protocol.
- •Major trauma including major surgery (such as abdominal/cardiac/thoracic surgery) within 4 weeks of administration of the study drug. Minimally invasive procedures such as biopsies are not considered as exclusion criteria.
- •Serious, non-healing wound, ulcer, or bone fracture.
- •Allergy to study medication or excipients in study medication.
- •Any anti-cancer therapy (e.g. cytotoxic chemotherapy, immunotherapy, radiation, surgery, etc.) within 3 weeks before [68Ga]Ga-OncoFAP-PET/CT scan
- •Subject has received, or is scheduled to receive, another investigational medicinal product (IMP) from 1 month before [68Ga]Ga-OncoFAP injection to end of study participation.
研究组 & 干预措施
Cohort A
3 female + 3 male patients with a primary tumor only
干预措施: [68Ga]Ga-OncoFAP administration (Drug)
Cohort B
Patients with a primary tumor and/or advanced/metastatic disease with a quantifiable number of lesions
干预措施: [68Ga]Ga-OncoFAP administration (Drug)
结局指标
主要结局
Safety (AE)
时间窗: Throughout study, until a maximum of 8 days after the completion of each patient
Safety of administration of 68Ga-OncoFAP, assessed based on Common Toxicity Criteria (CTCAE version 5.0)
Cohort A: Dosimetry - Effective dose equivalent (mSv)
时间窗: Assessed on day 1
Effective dose equivalent (mSv) of normal organs following administration of a single dose of \[68Ga\]Ga-OncoFAP, for patients in cohort A
Cohort A: Dosimetry - Absorbed doses (mGy)
时间窗: Assessed on day 1
Absorbed doses (mGy) of normal organs following administration of a single dose of \[68Ga\]Ga-OncoFAP, for patients in cohort A
次要结局
- Biodistribution profile: SUVmax(Assessed on day 1)
- Immunopathology staining(Assessed on day 1)
- PK(Assessed on day 1)
- Biodistribution profile: SUVmean(Assessed on day 1)
- Biodistribution profile: SUVsd(Assessed on day 1)
- Excretion(Assessed on day 1)
- Lesion detection rate(Assessed on day 1)