Kenyon Sweeney

Role: SVP General Manager at Agendia
Location: Salt Lake City, UT, US
LinkedIn followers: 500 followers

General Business & ManagementView LinkedIn profile

About Kenyon Sweeney

Highly motivated, results driven executive leader with a documented history of driving…

Experience

SVP General Manager
Agendia
Jan 2022 — Present

Education

Taylor University
Bachelors of Arts, Communiations
Westminster University
Masters of Business Administration, Entrepreneurship
Quinlan School of Business, Loyola University Chicago
Health Care Quality Improvement Institute

Skills

Critical Care
Diabetes
Sales Management
Product Management
Pharmacy
Healthcare Management
Neurology
Pharmaceutical Sales
Dermatology
Orthopedic
Medical Devices
Oncology
Internal Medicine
Rheumatology
Hematology
Vascular
Sales Operations
Cardiology
Sales Force Development
Urology
Leadership
Pharmaceutical Industry
Project Management
Capital Equipment
Hardware Diagnostics
Selling Skills
Managed Care
Hospitals
Ob/Gyn
Gastroenterology
Sales Effectiveness
Product Launch
Medicine
Infectious Diseases
Sales
Surgeons
Hospital Sales
Biotechnology
Pulmonology
Physicians

Contact information

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Work email
•••••@agendia.com
Personal email
•••••@•••••.com
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Current company

Agendia

Biotechnology · 224 employees · Founded 2003 · Irvine, California, United States

Agendia, a precision oncology company, helps physicians and patients make personalized treatment decisions in early-stage breast cancer. MammaPrint® (MP), 70-gene breast cancer recurrence assay, is the only FDA-cleared (microarray) risk of recurrence test and is CE marked (IVDR-certified). BluePrint®(BP), 80-gene molecular subtyping assay, evaluates the underlying biology of a tumor to determine growth drivers. MP+BP are commercially available genomic tests, supported by clinical, guideline, peer-reviewed, and real-world evidence. They can be ordered on core biopsies or surgical specimens.* *FDA Intended Use: the test is performed for breast cancer patients with Stage I or Stage II disease with tumor size ≤5.0cm and lymph node negative. The MP FFPE result is indicated for use by physicians as a prognostic marker only, along with other clinicopathological factors. Coverage criteria for majority of US health plans include early-stage breast cancer, tumor size less than or equal to 5.0cm (≤5.0cm), up to 3 positive lymph nodes, independent of receptor status, as validated in the 6,693 patient MINDACT trial. IVDR-CE mark Intended Use: you are a female breast cancer patient with Stage I or Stage II disease who is lymph node negative or lymph node positive with up to 3 positive nodes and for patients with stage III disease. The MP FFPE result is indicated for use by physicians and should be interpreted with other clinico-pathological factors. BP was developed and its performance characteristics determined by Agendia. It has not been cleared or approved by the US FDA, which determined that such clearance or approval is not necessary. This test is used for clinical purposes. It should not be regarded as investigational or for research. This test was performed at Agendia, Inc (05D10•••50), which is certified under CLIA as qualified to perform high-complexity clinical laboratory testing. It is CE-marked for use in Europe. Social media policy: agendia.com/legal-compliance

agendia.com

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About Kenyon Sweeney

Experience

SVP General Manager

Education

Taylor University

Westminster University

Quinlan School of Business, Loyola University Chicago

Skills

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