Precision Cancer Medicine for Advanced Cancer Through High-throughput Sequencing
Recruiting
Observational Study
Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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
18 and older
Sex
Any
Study type
Observational
Participants needed
1,000 (estimated)
Sponsor
Ohio State University Comprehensive Cancer Center · Other
Who this trial is looking for
This trial is looking for patients with cancer who can provide tumor tissue for research. Participating involves undergoing a biopsy or surgery to obtain this tissue.
Are You a Good Fit for This Trial?
You may be able to join if
I have been diagnosed with cancer.
I have a tumor that can be biopsied.
I can undergo a tissue biopsy or surgery.
I am undergoing routine surgery where leftover tissue can be used for research.
I am a woman or a member of a minority group.
I have multiple cancers.
I have a family history of cancer.
You may not be able to join if
The doctor says I am not fit enough for a biopsy.
I am currently incarcerated.
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 a few quick questions to see if you may meet the eligibility requirements.
Precision Cancer Medicine for Advanced Cancer Through High-throughput Sequencing
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
1. A histologically or cytologically confirmed diagnosis of cancer
2. Patients with any malignancy.
3. Patients must have tumor suitable for research tumor biopsy (as assessed by trained specialists in interventional radiology) and Patients are medically fit to undergo a tissue …
Inclusion Criteria:
1. A histologically or cytologically confirmed diagnosis of cancer
2. Patients with any malignancy.
3. Patients must have tumor suitable for research tumor biopsy (as assessed by trained specialists in interventional radiology) and Patients are medically fit to undergo a tissue biopsy or surgical procedure to get tumor tissue OR If Patients do not have a tumor suitable for biopsy but have another tissue available for molecular evaluation.
OR Patients are undergoing standard of care surgeries or procedures where fresh specimens will be first used for routine pathologic assessment and only then will leftover tissue be used for research purposes.
4. Procedure-specific signed informed consent prior to initiation of any study-related procedures.
5. Women and minorities are included in this protocol.
6. Patients with multiple malignancies remain eligible.
7. Patients with an inherited cancer syndrome or a medical history suggestive of an inherited cancer syndrome remain eligible.
Exclusion Criteria:
1. It is the enrolling study physicians discretion to decide if a patient is not fit enough to undergo tissue biopsy.
2. Patients who are incarcerated are not eligible to participate.
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