jRCT2031250565招募中不适用
A Modular Phase I/IIa, Open-label, Multi-centre Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of AZD0516 as Monotherapy and in Combination with Anti-cancer Agents in Participants with Metastatic Prostate Cancer (SEACLIFF) (SEACLIFF)
未提供0 个研究点目标入组 8 人开始时间: 待定
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 8
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
入排标准
- 年龄范围
- 18age old over 至 No limit(—)
- 性别
- All
入选标准
- •Histologically or cytologically confirmed diagnosis of metastatic adenocarcinoma of the prostate. Focal high grade neuroendocrine features are permitted.
- •Measurable PSA 1 mcg/L or more (1 ng/mL or more).
- •Surgically or medically castrated with serum testosterone levels 50 ng/dL or less (1.75 nmol/L or less) within 28 days or less before treatment allocation. Ongoing androgen deprivation therapy (ADT) with a gonadotropin releasing hormone (GnRH) modulator for participants who have not undergone bilateral orchiectomy must be initiated at least 2 weeks prior to consent and must continue throughout the study.
- •Eastern cooperative oncology group (ECOG) performance status of 0 or
- •Adequate organ and marrow function in the absence of blood transfusion or growth factor support (within 21 days prior to the scheduled first dose of study intervention).
- •Provision of baseline archival or newly obtained formalin-fixed paraffin-embedded (FFPE) tumour sample is mandatory.
- •Documented current evidence of metastatic prostate cancer
- •Documented mCRPC progression at screening as assessed by the investigator with at least one of the following criteria:
- •PSA progression defined by a minimum of 3 rising PSA levels with an interval of or more 1 week between each determination. The PSA value at the screening visit should be 1 mcg/L or more (1 ng/mL).
- •Radiographic disease progression in soft tissue based on response evaluation criteria in solid tumors (RECIST) v1.1 criteria with or without PSA progression as per prostate cancer working group 3 (PCWG3).
- •Radiographic disease progression in bone defined as the appearance of 2 or more new bone lesions on a bone scan as per PCWG3 with or without PSA progression.
排除标准
- •Cancer related spinal cord compression, or brain metastases unless asymptomatic, treated and stable and not requiring continuous corticosteroids at a dose of more 10 mg prednisone/day or equivalent for at least 4 weeks prior to study enrolment.
- •History of leptomeningeal carcinomatosis.
- •Unresolved toxicities of Grade 2 or more (National Cancer Institute Common Terminology Criteria for Adverse Events v5.0) from prior therapy (excluding vitiligo, alopecia, and endocrine disorders that are controlled with replacement hormone therapy).
- •Uncontrolled intercurrent illness within the last 12 months.
- •Cardiovascular disorder (History of arrhythmia, uncontrolled hypertension, symptomatic hypotension, history of brain perfusion problems, symptomatic heart failure, prior or current cardiomyopathy, severe valvular heart disease)
- •History of malignancy
- •History of non-infectious interstitial lung disease (ILD)/pneumonitis
- •Active infection exclusions, including tuberculosis and infections with Hepatitis B Virus (HBV), Hepatitis C Virus (HCV) or Human Immunodeficiency Virus (HIV).
- •Any known predisposition to bleeding
- •Clinically severe pulmonary compromise
- •Participants with Myelodysplastic syndrome (MDS)/Acute Myeloid Leukemia (AML) or with features suggestive of MDS/AML.
- •Previous treatment with a STEAP2 targeting modality, chemotherapeutic agent that inhibits topoisomerase activity or metabolic enzymes.
研究者
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