PRINCETON, N.J.--(BUSINESS WIRE)--Advaxis, Inc. (NASDAQ: ADXS), a late-stage biotechnology company developing cancer immunotherapies, today announced that it will host its annual Investor & Analyst Day on Monday, June 12, at 1:00 p.m. in New York, NY. The event will feature presentations followed immediately by a reception.
|Advaxis Investor & Analyst Day|
|Monday, June 12, 2017|
1:00 – 4:00 p.m. ET, Reception from 4:00 – 5:00 p.m.
|Offices of Reed Smith|
|599 Lexington Avenue, 22nd Floor|
|New York, NY 10022|
At this year’s Investor & Analyst Day, Advaxis will focus on “Patients, Partnerships and Progress” with presentations centering around the following areas:
- Clinical Trial Update with Case Study Highlights
- Plans for Data Dissemination and Timelines
- Update on Advaxis’ Corporate Collaborations
- Research Update on the NEO and HOT Programs
- Progress Towards Regulatory Submission and Commercial Readiness
During the Investor & Analyst Day, several investigators involved in Advaxis’ ongoing clinical trials will highlight their experiences and case studies in an interactive clinical symposium. An update will be provided on the company’s global Phase 3 AIM2CERV study, as well as a planned potentially registrational quality study of axalimogene filolisbac for the treatment of metastatic cervical cancer. In addition, the team will review the plans to file for marketing authorization for axalimogene filolisbac in the European Union this year, an update on the clinical collaboration with Amgen, Inc. on ADXS-NEO and more.
Attendance and Participation
To register for the event, please visit: www.advaxis.com.
About Advaxis, Inc.
Located in Princeton, N.J., Advaxis, Inc. is a late-stage biotechnology company developing multiple cancer immunotherapies based on its proprietary Lm Technology™. Lm Technology, using bioengineered live attenuated Listeria monocytogenes (Lm) bacteria, is the only known cancer immunotherapy agent shown in preclinical studies to both generate cancer fighting T cells directed against cancer antigens and neutralize Tregs and myeloid-derived suppressor cells (MDSCs) that protect the tumor microenvironment from immunologic attack and contribute to tumor growth. Advaxis' lead Lm Technology immunotherapy, axalimogene filolisbac, targets HPV-associated cancers and currently has multiple clinical trials underway, including Phase 3 in invasive cervical cancer, Phase 2 in head and neck cancer, and Phase 2 in anal cancer. The FDA has granted axalimogene filolisbac orphan drug designation for each of these three clinical settings, as well as Fast Track designation for adjuvant therapy for high-risk, locally advanced cervical cancer (HRLACC) patients and a SPA for the Phase 3 AIM2CERV trial in HRLACC patients. Axalimogene filolisbac has also been classified as an advanced therapy medicinal product for the treatment of cervical cancer by the European Medicines Agency’s Committee for Advanced Therapies. Advaxis has two additional immunotherapy products: ADXS-PSA in prostate cancer and ADXS-HER2 in HER2 expressing solid tumors, in human clinical development. In addition, Advaxis and Amgen are developing ADXS-NEO, an investigational cancer immunotherapy treatment designed to activate a patient's immune system to respond against the unique mutations, or neoepitopes, contained in and identified from each individual patient's tumor, with plans to enter the clinic in 2017.
Advaxis Forward-Looking Statement
This press release contains forward-looking statements, including, but not limited to, statements regarding Advaxis’ ability to develop the next generation of cancer immunotherapies, and the safety and efficacy of Advaxis’ proprietary immunotherapy, axalimogene filolisbac. These forward-looking statements are subject to a number of risks including the risk factors set forth from time to time in Advaxis’ SEC filings including, but not limited to, its report on Form 10-K for the fiscal year ended October 31, 2016, which is available at http://www.sec.gov.
Any forward-looking statements set forth in this presentation speak only as of the date of this presentation. We do not intend to update any of these forward-looking statements to reflect events or circumstances that occur after the date hereof other than as required by law.
You are cautioned not to place undue reliance on any forward-looking statements.