To access the live webcast and subsequent archived recording of this and other company presentations, please visit the investor section of Aduro's website at www.aduro.com. The archived webcast will remain available for replay on Aduro’s website for 30 days.
Details of the ADU-S100 (MIW815)
|Abstract 2507:||Phase 1b study of MIW815 (ADU-S100) in combination with spartalizumab (PDR001) in patients with advanced/metastatic solid tumors or lymphomas.|
|Presenter:||Dr. Funda Meric-Bernstam, MD Anderson Cancer Center|
|Oral Abstract Session:||Developmental Immunotherapy and Tumor Immunobiology|
|Date/Time/Location:||Sunday, June 2, 2019, 8:00 AM – 11:00 AM CDT in Hall D2|
|Dr. Meric-Bernstam’s presentation: 10:12 AM – 10:24 AM CDT|
To view this and other Aduro abstracts, please visit the
Cautionary Note on Forward-Looking Statements
This press release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding our intentions or current expectations concerning, among other things, the potential for our therapies and our ability to expand and drive our product pipeline alone or with collaborators. In some cases, you can identify these statements by forward-looking words such as “may,” “will,” “continue,” “anticipate,” “intend,” “could,” “project,” “expect” or the negative or plural of these words or similar expressions. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause actual results and events to differ materially from those anticipated, including, but not limited to, early or preliminary clinical trial results may not be predictive of future results, our history of net operating losses and uncertainty regarding our ability to achieve profitability, our ability to develop and commercialize our product candidates, our ability to use and expand our technologies to build a pipeline of product candidates, our ability to obtain and maintain regulatory approval of our product candidates, our ability to operate in a competitive industry and compete successfully against competitors that have greater resources than we do, our reliance on third parties, and our ability to obtain and adequately protect intellectual property rights for our product candidates. We discuss many of these risks in greater detail under the heading “Risk Factors” contained in our quarterly report on Form 10-Q for the quarter ended
|Investor Relations Contact:||Media Contact:|
|Noopur Liffick||Aljanae Reynolds|
Source: Aduro Biotech, Inc.