Advaxis News Releases

Date Title and Summary Additional Formats
March 16, 2021 Advaxis Reports First Quarter Ended January 31, 2021 Financial Results and Provides a Business Update
Continued enrollment in expanded ADXS-503 HOT program in NSCLC to explore potential to enhance and/or restore sensitivity to checkpoint inhibitors ADXS-503 Phase 1/2 trial data presented at SITC demonstrated disease control rate of 67% and overall response rate of 17% in first six evaluable
March 12, 2021 Advaxis to Present at the American Association for Cancer Research (AACR) 2021 Annual Meeting
PRINCETON, N.J., March 12, 2021 (GLOBE NEWSWIRE) -- Advaxis, Inc. (Nasdaq: ADXS), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, and Precision for Medicine, a specialized services company supporting next generation approaches to
January 25, 2021 Advaxis Reports Fiscal Year 2020 Financial Results and Provides a Business Update
Enrolling strategic expansion of ADXS-503 HOT program in NSCLC to explore potential to enhance and/or restore sensitivity to checkpoint inhibitors SITC presentation from ongoing ADXS-503 Phase 1/2 clinical trial demonstrated disease control rate of 67% and overall response rate of 17% in first six
January 19, 2021 Advaxis Announces Receipt of Funding Milestone Payment Under ADXS-HER2 Licensing Agreement with OS Therapies
Non-dilutive capital strengthens balance sheet to further advance ADXS-HOT neoantigen program PRINCETON, N.J., Jan. 19, 2021 (GLOBE NEWSWIRE) --  Advaxis, Inc.  (NASDAQ: ADXS), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, today
December 22, 2020 Advaxis Announces Listing Transfer to Nasdaq Capital Market and Additional 180-day Extension by Nasdaq to Regain Compliance with Minimum Bid Price Rule
PRINCETON, N.J., Dec. 22, 2020 (GLOBE NEWSWIRE) -- Advaxis, Inc. (Nasdaq: ADXS), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, today announced that it received a positive determination from the Nasdaq Stock Market granting
November 27, 2020 Advaxis, Inc. Announces Closing of $9.2 Million Public Offering
PRINCETON, N.J., Nov. 27, 2020 (GLOBE NEWSWIRE) --  Advaxis, Inc. (Nasdaq: ADXS)  (the “Company”), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, today announced the closing of an underwritten public offering of 26,666,666 shares
November 24, 2020 Advaxis, Inc. Announces Pricing of $8 Million Public Offering
PRINCETON, N.J., Nov. 24, 2020 (GLOBE NEWSWIRE) --  Advaxis, Inc. (Nasdaq: ADXS)  (the “Company”), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, today announced the pricing of an underwritten public offering of (i) 26,666,666
November 23, 2020 Advaxis, Inc. Announces Proposed Public Offering of Common Stock and Warrants to Purchase Common Stock
PRINCETON, N.J., Nov. 23, 2020 (GLOBE NEWSWIRE) --  Advaxis, Inc. (Nasdaq: ADXS)  (the “Company”), a clinical-stage biotechnology company focused on the development and commercialization of immunotherapy products, today announced that it intends to offer and sell shares of its common stock and
November 9, 2020 Advaxis Presents Updated Data from Ongoing ADXS-503 Phase 1/2 Lung Cancer Trial at the 2020 Society for Immunotherapy of Cancer (SITC) Annual Meeting
Disease control rate of 67%  and overall response rate of 17%  in first six evaluable patients   with immediate prior progression  on KEYTRUDA ® Biomarker data confirms on-mechanism activation of innate and adaptive immune responses to ADXS-503 ADXS-503 appeared safe and well tolerated as a
October 26, 2020 Advaxis’ ADXS-503 (HOT Lung) Demonstrates Pronounced and Sustained Tumor Control in Ongoing Phase 1/2 Lung Cancer Trial
Disease control rate of 67% in first six evaluable patients  who had progressed on KEYTRUDA Approximate 50% improvement  in  disease control rate  versus the rate s  reported  in  other checkpoint rechallenge studies Durable, sustained  tumor control  of  over  43 and   33 weeks observed in  first
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