TEL AVIV, Israel, Nov. 02, 2016 (GLOBE NEWSWIRE) -- VBL Therapeutics (Nasdaq:VBLT), a clinical-stage biotechnology company focused on the discovery, development and commercialization of first-in-class treatments for cancer, today announced that it will host a conference call and live audio webcast on Thursday, November 10, 2016 at 8:30 a.m. Eastern Time to report third quarter 2016 financial results.
| Thursday, November 10th @ 8:30am Eastern Time | |||
| Domestic: | 888-283-6901 | ||
| International: | 719-325-2324 | ||
| Conference ID: | 6160786 | ||
| Webcast: | http://edge.media-server.com/m/p/wbqvkh6p | ||
| Replays, available through November 24: | |||
| Toll Free: | 844-512-2921 | ||
| International: | 412-317-6671 | ||
| Conference ID: | 6160786 | ||
About VBL
Vascular Biogenics Ltd., operating as VBL Therapeutics, is a clinical stage biopharmaceutical company focused on the discovery, development and commercialization of first-in-class treatments for cancer. The Company’s lead oncology product candidate, VB-111, is a first-in-class, targeted anti-cancer gene-therapy agent that is positioned to treat a wide range of solid tumors. VB-111 is conveniently administered as an IV infusion once every two months. It has been observed to be well-tolerated in >200 cancer patients and we have observed its efficacy signals in an “all comers” Phase 1 trial as well as in three tumor-specific Phase 2 studies. The mechanism of VB-111 combines blockade of tumor vasculature with an anti-tumor immune response. This mechanism retains activity regardless of baseline tumor mutations or the identity of the pro-angiogenic factors secreted by the tumor. VB-111 is currently being studied in a Phase 3 pivotal trial for Recurrent Glioblastoma (rGBM). The trial is being conducted under an FDA Special Protocol Assessment (SPA), and VB-111 has obtained fast track and Orphan designations.