Register Now: Beyond EDC: Designing a Connected Data Strategy for Predictive Clinical Development
|Articles|August 19, 2010

US Oncology Helps Deliver Latest Cancer Therapies

US Oncology

, Inc.,an integrated oncology company, announced that it has played a role in the development of 42 novel cancer therapies approved by the US Food and Drug Administration (FDA).

Tasigna (nilotinib) capsules, a medicine developed by Novartis Pharmaceuticals Corporation, was the most recent therapy to benefit from clinical trials conducted in part by physicians and patients within the US Oncology Research network. The drug, which was recently approved by the FDA, is for the treatment of adult patients with newly diagnosed Philadelphia chromosome-positive chronic myeloid leukemia (Ph+CML) in chronic phase.

US Oncology is affiliated with 500 sites of care throughout the nation and its network treats about 850,000 patients a year.


Related to this article

What Needs to Happen Beyond the Clinical Trial Modernization Act
In this video interview, Kent Thoelke, CEO of Paradigm Health, calls for safe harbor protections, CMS reimbursement safeguards, and funding mechanisms modeled on EHR meaningful use to help community and rural institutions participate in research on par with academic centers.
Building AI Assistants Clinical Trial Teams Can Trust: Q&A with E.K. Koh, Suvoda
In this Q&A, E.K. Koh, chief product officer at Suvoda, discusses what separates a trustworthy AI assistant from one that adds risk, why curated clinical knowledge matters more than general-purpose flexibility, and what safeguards must be in place when assistants move from answering questions to taking actions in clinical trial systems.