No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
7 and older
Sex
Any
Study type
Observational
Participants needed
10,000 (estimated)
Sponsor
Shu Mei Kato · Other
Who this trial is looking for
This trial is looking for people with cancer to learn about how personalized treatments work for them. Participants will provide medical information and may have research tests done on their blood or other samples to help understand their cancer better.
Are You a Good Fit for This Trial?
You may be able to join if
I am willing to give informed consent or assent
You may not be able to join if
I am unable to give informed consent or assent
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The purpose of this study is to learn more about personalized cancer therapy including response to treatment and side effects. Information about the tests and treatments a person received, or will receive, for their cancer will be collected from medical records to help the researchers determine whether or not patients respond better when their physicians choose to treat them according to the genet…
The purpose of this study is to learn more about personalized cancer therapy including response to treatment and side effects. Information about the tests and treatments a person received, or will receive, for their cancer will be collected from medical records to help the researchers determine whether or not patients respond better when their physicians choose to treat them according to the genetic makeup of their tumor. Optional research tests may be performed on tissue, body cavity fluid, blood or urine provided, discarded biological samples taken during routine care that would normally be disposed of and not saved, or on blood samples collected for this study. These research tests will be used to create a "profile" of the collected specimens which will describe unique characteristics about the genes involved in a person's cancer. The tests will also help researchers look for biomarkers that may help predict how people respond to treatment.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Must be willing to provide informed consent, parent permission, or assent
Exclusion Criteria:
* Subjects unable to give informed consent, parent permission, or assent
Inclusion Criteria:
* Must be willing to provide informed consent, parent permission, or assent
Exclusion Criteria:
* Subjects unable to give informed consent, parent permission, or assent
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