A Study to Find a Suitable Dose of ASP4396 in Adults With Solid Tumors - Trial NCT06364696

Timeline & Enrollment

Primary Outcome

Incidence of Dose Limiting Toxicities (DLTs) for ASP4369,Number of Participants with Adverse Events (AEs),Number of Participants with Serious Adverse Events (SAEs),Number of Participants with laboratory value abnormalities and/or AEs,Number of Participants with electrocardiogram (ECG) abnormalities and/or AEs,Number of Participants with vital sign abnormalities and/or AEs,Number of Participants with physical exam abnormalities and/or AEs,Number of Participants with Eastern Cooperative Oncology Group (ECOG) performance status score

Summary

Genes contain genetic code which tell the body which proteins to make. Some 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.
 
 ASP4396 is being developed as a potential new treatment for solid tumors in people who have
 the G12D mutation in their KRAS gene. ASP4396 is not currently available as a treatment for
 the public. In this study, researchers will learn how ASP4396 is processed by and acts upon
 the body. This information will help find a suitable dose and to check for potential medical
 problems from ASP4396.
 
 In this study, ASP4396 is being given to humans for the first time.
 
 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. They may have been
 previously treated with standard therapies or refused to receive those treatments.
 
 The main aims of the study are to check the safety of ASP4396, how well people cope with
 medical problems during the study (how well it is tolerated), and to find a suitable dose of
 ASP4396.
 
 This is an open-label study. This means that people in this study and clinic staff will know
 that they will receive ASP4396.
 
 This study will be in 2 parts.
 
 Part 1 is called Dose Escalation. Different small groups of people will receive lower to
 higher doses of ASP4396. For each dose, all medical problems will be recorded. The first
 group will receive the lowest dose of ASP4396. A medical expert panel will check the results
 and decide if the next group can receive a higher dose of ASP4396. The panel will do this
 until all groups have taken ASP4396 or until suitable doses have been selected for Part 2.
 
 Part 2 is called Dose Expansion. Other different small groups of people will receive ASP4396
 with the most suitable doses worked out from Part 1. This will help find a more accurate dose
 of ASP4396 to use in future studies.
 
 In both parts of the study, ASP4396 will be given through a vein. This is called an infusion.
 Each treatment cycle is 21 days long. People will continue treatment until: they have medical
 problems from the treatment they can't cope with (can't tolerate); their cancer gets worse;
 they start other cancer treatment; or they ask to stop treatment.
 
 People will visit the clinic on certain days during their treatment, with extra visits during
 the first 2 cycles of treatment. The study doctors will check for any medical problems from
 ASP4396. Also, people in the study will have a health check including blood tests. On some
 visits they will also have scans to check for any changes in their cancer. Tumor samples will
 be taken at certain visits during treatment with the option of a tumor sample being taken
 after treatment has finished.
 
 People will visit the clinic about 7 days after they stop treatment. They will be asked about
 any medical problems and will have a health check including blood tests.
 
 After this, people will visit the clinic for a health check several times. The number of
 visits and checks done at each visit will depend on the health of each person and whether
 they completed their treatment or not.
 
 After treatment has finished, people in the study will be followed up for up to 45 weeks.

ICD-10 Classifications