Trial purpose
Genes contain genetic code which tell the body which proteins to make. Many types of cancer are caused by changes, or mutations, in a gene called KRAS. Researchers are looking for ways to stop the actions of abnormal proteins made from the mutated KRAS gene. The so-called G12D mutation in the KRAS gene is common in people with some solid tumors.
ASP3082 is a potential new treatment for solid tumors in people who have the G12D mutation in their KRAS gene. Before ASP3082 is available as a treatment, the researchers need to understand how it is processed by and acts upon the body. This information will help find a suitable dose and to check for potential medical problems from the treatment.
Who May Participate
People in this study will be adults with locally advanced, unresectable or metastatic solid tumors with the G12D mutation in their KRAS gene. Locally advanced means the cancer has spread to nearby tissue. Unresectable means the cancer cannot be removed by surgery. Metastatic means the cancer has spread to other parts of the body. The key reasons people cannot take part are if they have symptomatic or untreated cancers in the brain or nervous system, their cancer has spread to the thin tissue that covers the brain and spinal cord (leptomeningeal disease), or they have recently had other active cancers that required treatment.
For ASP3082 combination therapy with Nab-P+GEM or FOLFIRINOX: Participant must have mPDAC that has not been previously treated with chemotherapy. If a participant received (neo)adjuvant therapy, tumor recurrence or disease progression must have occurred at least 6 months after completing the last dose of the (neo)adjuvant therapy.
试验摘要
The main aims (primary objectives)
- To check the safety of ASP3082 by itself and together with the other study treatments, and how well it is tolerated.
- To find a suitable dose of ASP3082 by itself and together with the other study treatments.
Other aims (secondary objectives)
- To check how ASP3082 is processed by the body (pharmacokinetics, or PK).
- To check how well ASP3082 controls tumors.
How the aims are carried out (endpoints)
- Recording medical problems that happen during the study after receiving ASP3082, whether they were caused by ASP3082 or not. This may include abnormal results from lab tests, medical examinations and electrocardiograms (ECGs).
- Checking if medical problems or abnormal lab test results that may be caused by ASP3082 are serious enough to stop increasing the dose.
- Checking blood levels of ASP3082 over time to learn how long it takes to get into the blood, spread through the body and be cleared by the body. Also checking if ASP3082 is broken down by the body.
- Using scans to check if tumors shrink or disappear over time, after treatment with ASP3082.
- Checking for changes in KRAS G12D protein levels on tissue samples.
获取更多信息
关于正在招募参与者的 在既往接受过治疗的实体肿瘤成人患者中评估 ASP3082 的研究,您是否想了解更多临床试验中心相关信息?请在右侧填写您的信息联系我们,我们将予以回复。
地点
常见问题
虽然某些临床试验可能侧重于更晚期的癌症,但许多试验对处于不同癌症阶段的患者开放。每项研究都有关于参与资格的规定。例如,只有特定年龄段的患者或患有特定类型肿瘤的患者才能参与。
有时,研究人员希望参与者在临床试验期间继续接受当前治疗。有时,您可能需要暂停当前的治疗。如果研究性治疗无效,您通常可以恢复原有的治疗方案。
在癌症临床试验中,只有当该类癌症尚无其他治疗方法时,才会使用安慰剂。这有助于将研究性治疗与安慰剂进行比较。安慰剂在癌症试验中很少使用,因为通常会采用最佳可用疗法,即所谓的“标准治疗方案”。
您的医生可能并不了解所有可供您参与的临床试验机会。请与您的医生或其他医疗服务提供者讨论您所找到的临床试验信息。他们可以帮助您判断临床试验是否适合您。若您在本网站未找到任何试验选择,我们建议您访问在线公共注册网站,例如 ClinicalTrials.gov 查看各种可参与的临床试验。
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