Pan-tumor MRD Study
- Conditions
- Muscle Invasive Bladder Urothelial CarcinomaEsophageal CancerGastric and Gastroesophageal Junction (GEJ) AdenocarcinomaMelanoma (Skin Cancer)NSCLC (Non-small Cell Lung Cancer)Pancreatic (Exocrine Only)Mix of Solid Tumors (MOST)
- Registration Number
- NCT06605404
- Lead Sponsor
- Flatiron Health
- Brief Summary
The purpose of this observational study is to collect clinical information, blood, and tumor tissue samples from participants diagnosed with stage I, stage II, or operable stage III cancer in select solid tumors. The information collected will be used to develop tests to better understand cancer, for example, to improve cancer detection and to assess the risk of cancer coming back.
Participants will receive routine standard of care from their doctor and their involvement is expected to last for approximately five and a half (5.5) years.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 1350
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood and tissue biospecimen registry Observation from enrollment to 5.5 years after enrollment To establish a blood and tissue biospecimen resource in participants with operable solid tumors, with clinical, lab, radiographic, and pathology annotation for the discovery, development, and validation of MRD assays.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Taylor Cancer Research Center
🇺🇸Maumee, Ohio, United States
Taylor Cancer Research Center🇺🇸Maumee, Ohio, United StatesJennifer MartinezContact419-479-5605jmartinez@toledoclinic.com