Patient Derived Preclinical Models
Recruiting at 1 trial location
CT
TM
Overseen ByTanya M. Schnick
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Mayo Clinic
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Trial Summary
What is the purpose of this trial?
Study goal is to collect tumor specimens that may inform cancer biology to eventually improve outcomes for patients with cancer. This proposal represents a highly collaborative effort to support cancer research with the goal of developing novel therapeutic strategies using patient derived preclinical models. This study is being done to collect samples of tumor tissues, matched normal tissue when possible, and approximately 50 mL of blood.
Research Team
AS
Aaron S. Mansfield, M.D.
Principal Investigator
Mayo Clinic
Eligibility Criteria
Inclusion Criteria
18 years of age and older
Patient is a good medical candidate for a standard of care or research biopsy or surgical procedure to obtain tissue
Exclusion Criteria
You have a serious heart or lung condition that may put you at risk during the study.
The biopsy procedure is safe and poses no significant risk to the patient.
Have a contraindication to percutaneous biopsy including:
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Treatment Details
Interventions
- Tissue Collection
Participant Groups
3Treatment groups
Experimental Treatment
Group I: Tissue CollectionExperimental Treatment1 Intervention
Research tissue specimen will be obtained during the patient's clinical biopsy or clinical tumor resection, if feasible.
Group II: Buccal SwabExperimental Treatment1 Intervention
Buccal swab may be requested, if necessary, to generate germline data.
Group III: Blood CollectionExperimental Treatment1 Intervention
Up to 50 mL of research blood will be drawn around the time of the procedure. Additional blood may be collected in selected cases, as warranted, to monitor disease recurrence/remission or perform additional testing
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Who Is Running the Clinical Trial?
Mayo Clinic
Lead Sponsor
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Recruited
3,221,000+
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