CA-AGENDIA
6.1.2022 21:43:03 CET | Business Wire | Press release
Agendia, Inc. , a commercial stage company focused on precision oncology for breast cancer, today announced the appointment of healthcare industry veterans Suja Chandrasekaran, MS and Scott Mendel, MBA to the Company’s Board of Directors.
“We are pleased to be expanding Agendia’s Board of Directors with the appointment of two accomplished industry executives,” said Mark Straley, Chief Executive Officer of Agendia. “With combined decades of leadership and results-driven performance, Suja and Scott will provide Agendia with invaluable guidance, informed by extensive executive experience. As we continue to deliver on our goal to provide crucial genomic information to physicians and their patients to improve care, we look forward to tapping into their diverse expertise.”
“Suja’s reputation for growing, scaling, and transforming global businesses with data-driven go-to-market strategies and business vision is unparalleled,” said Patrick J. Balthrop, Chairman of the Board at Agendia. “Similarly, Scott’s executive insights and deep financial experience will be integral assets as we position the business for ongoing operational excellence and commercialization to best serve the breast cancer community.”
Suja Chandrasekaran, MS
Ms. Chandrasekaran joins Agendia’s Board with over 25 years of experience in building businesses in retail, consumer, manufacturing, and healthcare. Her specialties include risk management, ESG, and the employment of digital capabilities to drive growth and revenue. Ms. Chandrasekaran currently serves as Senior Executive Vice President, Chief Digital and Information Officer at CommonSpirit Health, where she leads the digitization of healthcare focusing on unleashing the power of data with AI to provide rich patient and provider experiences. Previously she was the Global Chief Technology Officer at Walmart Inc. and Kimberly-Clark Corporation. She also serves on the boards of American Eagle Outfitters and Blume Global Technologies.
Ms. Chandrasekaran earned her Master of Business Systems at Monash University in Melbourne, Australia and her Bachelors in Electrical Engineering from the University of Madras, India. She holds many prestigious honors recognizing her technology and digital leadership, including her recent induction into the CIO Hall of Fame.
“Agendia is harnessing impressive science to deliver state-of-the-art solutions to the breast cancer community and I’m honored to contribute to the company’s meaningful mission,” said Chandrasekaran. “I am especially excited by the technology supporting MammaPrint and BluePrint genomic tests as well as the potential future expansion into next generation sequencing and digital AI pathology solutions to follow the patient throughout her journey.”
Scott Mendel, MBA
Mr. Mendel is an industry veteran with over 25 years in public and private corporate leadership, notably in healthcare, software, and diagnostics. Most recently, Mr. Mendel served as the Chief Executive Officer of GenMark Diagnostics, overseeing a period of rapid growth and the process that ultimately led to the company’s purchase by Roche Diagnostics. Mr. Mendel previously served as GenMark’s Chief Operating Officer and Chief Financial Officer, leveraging his deep expertise in finance and manufacturing scale-up, fund raising and investor relations, and general commercial operations and strategy.
Prior to GenMark, Mr. Mendel held senior-level leadership positions with The Active Network and GE Healthcare. He serves as Audit Committee Chair and Compensation Committee member at Akoya Biosciences and is a member of Board of Advisors at Specific Diagnostics and Visby Medical. He holds a Bachelor of Science in finance from Indiana University and a Master of Business Administration from Northwestern University’s Kellogg School of Management.
“I am thrilled to join Agendia’s Board of Directors and to partner with the impressive, mission-driven genomic specialists, operational talent, and industry leaders in our shared vision,” said Mendel. “I look forward to contributing my executive expertise as Agendia pursues its objectives to advance genomic testing in breast cancer and improve outcomes for patients.”
The Agendia Board and management team is committed to bringing in and utilizing strong executive and operational talent at all levels to align with the superior execution and focus on propelling the Company’s advancement in all areas. We believe this dedication translates into exceptional science, actionable and transformative research, and bringing innovative new products to market to ensure breast cancer patients, their families and their physicians have access to the information they need to make the best decisions about the treatment journey. Learn more here .
About Agendia
Agendia is a mission-driven company focused on enabling optimized decision-making by providing physicians with next-generation diagnostic and information solutions that can be used to help improve outcomes for breast cancer patients worldwide. The company currently offers two commercially-available genomic profiling tests that help surgeons, oncologists and pathologists to personalize treatment for women at critical intervention points throughout their patient journey.
MammaPrint® is a 70-gene prognostic test that, along with other clinicopathologic factors, determines a specific patient’s breast cancer recurrence risk. BluePrint® is an 80-gene molecular subtyping test that identifies the underlying biology of an individual breast cancer to provide information about its behavior, long-term prognosis and potential response to systemic therapy. Together, MammaPrint® and BluePrint® provide a holistic view of an individual patient’s breast cancer, enabling physicians to objectively select the best treatment plan.
For more information on Agendia’s assays and ongoing trials, please visit www.agendia.com .
View source version on businesswire.com: https://www.businesswire.com/news/home/20220106005853/en/
Link:
About Business Wire
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Galderma Receives U.S. FDA Approval for Differin® Epiduo® Acne Gel Prescription-to-OTC Switch22.5.2026 18:25:00 CEST | Press release
A unique Prescription-to-OTC switch in acne care, this approval expands access to a dermatologist-trusted, prescription-strength treatment for millions of acne sufferers ages 12 years and older Backed by more than 15 years of real-world dermatologist use and a robust clinical research program, this milestone demonstrates the depth of science behind the Differin® and Epiduo® heritage Adapalene plus benzoyl peroxide (0.1/2.5%) was the first FDA-approved, stable, fixed- dose prescription acne treatment to combine of benzoyl peroxide with a retinoid, and is now available over-the-counter The formulation is engineered to target multiple causes of acne more effectively than either of its individual active ingredients alone Galderma (SIX: GALD), the pure-play dermatology category leader, today announced that the United States (U.S.) Food and Drug Administration (FDA) has approved Differin® Epiduo® Acne Gel (Adapalene 0.1% and Benzoyl Peroxide 2.5% Acne Treatment) for over-the-counter (OTC) us
Avanzanite Bioscience’s Partner Agios Announces PYRUKYND® (mitapivat) Approval in the European Union for Adults with Thalassaemia22.5.2026 16:18:00 CEST | Press release
Avanzanite will commercialise and distribute PYRUKYND in Europe under its exclusive agreement with Agios Avanzanite is committed to collaborating with local authorities in the EU to enable access to PYRUKYND for adult patients with thalassaemia Avanzanite Bioscience B.V., a rapidly growing commercial-stage European specialty pharmaceutical company focused on rare diseases, today reported that its partner, Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company headquartered in Cambridge, Massachusetts focused on delivering innovative medicines for patients with rare diseases, announced that the European Commission has granted marketing authorisation for PYRUKYND® (mitapivat), an oral pyruvate kinase (PK) activator, in adults for the treatment of anaemia associated with transfusion-dependent and non-transfusion-dependent alpha- or beta-thalassaemia, with an orphan medicinal product designation. This press release features multimedia. View the full releas
ICE Brent and ICE WTI Perpetual Futures to Launch on OKX22.5.2026 14:30:00 CEST | Press release
OKX, a blockchain technology and trading company serving more than 120 million customers globally,and Intercontinental Exchange (NYSE: ICE), one of the world's leading providers of financial market technology and data powering global capital markets including the New York Stock Exchange, today announced plans for OKX to launch perpetual futures based on ICE's Brent Crude and WTI Crude energy benchmarks. The products are expected to be available to trade on OKX’s platform in jurisdictions where OKX is licensed to offer perpetual futures products. The new OKX contracts represent a major step forward in expanding regulated access to global commodity markets through digital asset infrastructure. This first product collaboration between OKX and ICE comes after the companies established a strategic relationship in March 2026. ICE operates some of the world’s leading exchanges, clearing houses and market data services across energy, commodities, fixed income and equities markets. ICE’s future
Enhertu® Recommended for Approval in the EU by CHMP for Patients with Previously Treated HER2 Positive Metastatic Solid Tumors22.5.2026 14:00:00 CEST | Press release
Enhertu® (trastuzumab deruxtecan) has been recommended for approval in the European Union (EU) as a monotherapy for the treatment of adult patients with unresectable or metastatic HER2 positive (immunohistochemistry [IHC] 3+) solid tumors who have received prior treatment and who have no satisfactory treatment options. Enhertu is a specifically engineered HER2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/NYSE: AZN). The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) based its positive opinion on results from patients with HER2 positive (IHC 3+) tumors in three phase 2 trials including DESTINY-PanTumor02,DESTINY-Lung01 andDESTINY-CRC02 where Enhertu demonstrated clinically meaningful responses across a broad range of tumors. The recommendation will now be reviewed by the European Commission, which has the authority
Future Health Challenge Awards USD 300,000 to Early Detection and Population Health Sensing Tools on Sidelines of World Health Assembly22.5.2026 13:45:00 CEST | Press release
Global teams recognised in the Future Health Challenge for solutions designed to detect health risks earlier and support faster health system decisions Future Health – A Global Initiative by Abu Dhabi and MIT Solve announce the winners of the inaugural Future Health ChallengeWinning solution equips frontline health workers in low-resource settings with mobile clinical decision-support tools, enabling earlier detection and more effective care deliveryTeams competed for a USD 200,000 grand prize and two USD 50,000 runner-up awards on the sidelines of the 79th World Health Assembly in GenevaWinners recognised for solutions advancing anticipatory, data-driven health systems Three global teams developing early detection and real-time population health monitoring solutions have secured a total of USD 300,000 on the sidelines of the 79th World Health Assembly. The winning solutions address critical challenges in early detection, continuous population insight and more timely decision making, s
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom
