Validation of the MiCK Assay

Pierian Biosciences

Status: Terminated

Conditions: Mesothelioma, Small Cell Lung Cancer, NSCLC

Study type: Observational

Funder types: Industry

Identifiers

NCT01770665

MAYO1000

Details and patient eligibility

About

Testing Mayo Clinic cancer patients with the results being correlated with prior patient therapy, performance status, and extent of disease.

Full description

This study will be conducted in two phases.

During the Feasibility Phase, specimens from any tumor will be sent to the central DiaTech MiCK assay laboratory to determine the ease of sample acquisition, processing, transport, and assay interpretation.

Once DiaTech has completed analyses for the feasibility phase specimens and has confirmed that the sample acquisition, processing, transport, and assay interpretation are appropriate, we will proceed with the Demonstration Phase.

During the Mesothelioma Demonstration Phase, 20 mesothelioma samples will be assayed and the results will be correlated with prior patient therapy, performance status, and extent of disease.

Enrollment: 21 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 20 subjects diagnosed with mesothelioma and 10 diagnosed with any malignancy.

Exclusion criteria

• patients that a sample cannot obtained for testing.

Trial design

21 participants in 2 patient groups

Mesothelioma

all cancer types