Guest speakers scheduled to present at the event include:
Katherine Fuh, MD, PhD, Assistant Professor of Obstetrics and Gynecology, Center for Reproductive Health Sciences, Department of Obstetrics & Gynecology, Washington University School of Medicine
Greg Lemke, PhD, Professor, Molecular Neurobiology Laboratory, Françoise Gilot-Salk Chair, Salk Institute for Biological Studies
Amato J. Giaccia, PhD, Aravive Co-founder, Director, Jack, Lulu and Sam Willson Professor of Cancer Biology, Department of Radiation Oncology, Division of Radiation Biology, Stanford University School of Medicine
The webcast of the presentation will be available under “Presentations, Events, and Webcasts” in the Investors section of the Company’s website at www.aravive.com. A replay of the webcast will be available on the
Forward Looking Statements
This communication contains forward-looking statements (including within the meaning of Section 21E of the United States Securities Exchange Act of 1934, as amended, and Section 27A of the United States Securities Act of 1933, as amended), express or implied, concerning the Company's goals, intentions and expectations as to future plans or events, including statements regarding the Company’s intention to expand development in 2019 into additional tumor types. Forward-looking statements are based on current beliefs and assumptions that are subject to risks and uncertainties and are not guarantees of future performance. Actual results could differ materially from those contained in any forward-looking statement as a result of various factors, including, but not limited to, risks and uncertainties related to: the Company’s ability to expand development in 2019 into additional tumor types, the anticipated development strategy for AVB-S6-500 being successful, AVB-S6-500’s ability to have favorable results in clinical trials or receive regulatory approval, including its ability to meet the primary and secondary endpoint for the Phase 1b portion of the clinical trial and show a clinical benefit; potential delays in the Company's clinical trials due to regulatory requirements or difficulty identifying qualified investigators or enrolling patients; the risk that AVB-S6-500 may cause serious side effects or have properties that delay or prevent regulatory approval or limit its commercial potential; the risk that the Company may encounter difficulties in manufacturing AVB-S6-500; if AVB-S6-500 is approved, risks associated with its market acceptance, including pricing and reimbursement; potential difficulties enforcing the Company's intellectual property rights; the Company's reliance on its licensor of intellectual property and financing needs. The foregoing review of important factors that could cause actual events to differ from expectations should not be construed as exhaustive and should be read in conjunction with statements that are included herein and elsewhere, including the risk factors included in the Company's proxy statement/prospectus/information statement filed with the
Source: Aravive, Inc.