Plexxikon

Peter Hirth joins Trovagene's scientific advisory board

Friday, August 15, 2014 10:34 AM

Trovagene, a California-based developer of cell-free molecular diagnostics, has hired K. Peter Hirth, Ph.D., who joins the company's scientific advisory board. A pioneer in the field of personalized medicine, Hirth led the organizations that developed both Sutent and Zelboraf; two successful targeted cancer therapeutics.

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Plexxikon selects Clinipace to manage trials

Friday, March 18, 2011 10:51 AM

Plexxikon, a company focused on the discovery and development of novel small molecule pharmaceuticals to treat human disease, has selected Clinipace Worldwide, a digital CRO, to manage all aspects of four clinical trials comprising a phase I healthy volunteer study, a phase Ib rheumatoid arthritis (RA) study and two phase II oncology studies. 
  
“We chose Clinipace Worldwide to manage these important clinical trials based on Clinipace’s commitment to customer service,” said Paul Lin, MD, MBA, director of business development at Plexxikon. “Plexxikon’s programs are highly differentiated from its competition, and we needed a highly differentiated CRO to get the job done.”

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Plexxikon initiates phase II trial

Wednesday, March 9, 2011 10:50 AM

Plexxikon has treated its first patient in a phase II trial in Hodgkin lymphoma with PLX3397. This agent is an oral, selective inhibitor that down-modulates two key cell types thought to mediate the progression of Hodgkin lymphoma tumors: macrophages and mast cells.

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Daiichi Sankyo acquires Plexxikon

Tuesday, March 1, 2011 12:35 PM

In another sign that biotechnology companies with promising pipelines are able to forge rich buyout deals, Japanese pharmaceutical company Daiichi Sankyo has announced it will pay $805 million upfront and up to $130 million in near-term milestones for Plexxikon, a tiny oncology developer, according to Fierce Biotech.

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June 29

FDA and PatientsLikeMe collaborate to test social media adverse event reporting

Boston-area teaching hospitals launch web portal to attract life science companies

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The CenterWatch Monthly

July

Integrated research partnerships build momentum
Research function provides infrastructure, leverages large pool of health systems' patients and data

'Right to Try' laws challenge clinical trial process
20 states pass, 20 more pending allowing access to study drugs without FDA and IRB approval

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June

TransCelerate Biopharma turns three
High-profile consortium has made inroads fixing wasteful practices, but it still has more work ahead

Pharma industry improves its tarnished reputation
Delivering innovation, social responsibility will help rebuild trust

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