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Ayala Pharmaceuticals Inc ADXS

Ayala Pharmaceuticals, Inc. is a clinical-stage oncology company primarily focused on developing and commercializing small molecule therapeutics for patients suffering from rare and aggressive cancers, primarily in genetically defined patient populations. The Company's lead candidate is aspacytarabine (BST-236), a novel anti-metabolite for first line treatment in unfit acute myeloid leukemia (AML). Aspacytarabine (BST-236) is composed of cytarabine covalently bound to asparagine, acting as a pro-drug of cytarabine. It is also focused on the development and commercialization of proprietary Listeria monocytogenes (Lm)-based antigen delivery products. These efforts are primarily focused on the development of ADXS-504, a Lm-based therapy for early-stage prostate cancer.


PINL:ADXS - Post by User

Post by Humaniston Oct 26, 2020 9:17am
211 Views
Post# 31780490

SA ARTICLE: ADXS 12% DOWN DESPITE ADXS-503 SHOWING + RESULTS

SA ARTICLE: ADXS 12% DOWN DESPITE ADXS-503 SHOWING + RESULTSAdvaxis down 12% despite ADXS-503 shows sustained tumor control in mid-stage lung cancer trial
Oct. 26, 2020 8:46 AM ET|About: Advaxis, Inc. (ADXS)|By: Mamta Mayani, SA News Editor 

Advaxis (NASDAQ:ADXSannounces updated clinical results from the combination arm of its Phase 1/2 study evaluating ADXS-503 in combination with Merck's (NYSE:MRK) KEYTRUDA (pembrolizumab), an anti-PD-1 therapy in non-small cell lung cancer (NSCLC).

ADXS-503 is the first drug construct from the Company’s ADXS-HOT off-the-shelf, cancer-type specific, immunotherapy program.
Key data updates for the first 6 evaluable patients include:

Disease control rate of 67% (4/6 patients) and overall response rate of 17% (1/6 patients) achieved after immediate prior progression on KEYTRUDA.

Sustained and durable clinical benefit with the first two treated patients remaining on treatment for over 43 and 33 weeks.
Approximate 50% improvement observed in disease control rate versus the rates reported in other checkpoint rechallenge studies.

Stable disease (SD) confirmed on 13 week-scan in a patient with squamous NSCLC who received Pembrolizumab for ~15 months and SD on 6 week-scan in non-squamous NSCLC patient who receiving Pembrolizumab for ~14 months, including combination therapy with chemotherapy.
Shares are down 12% premarket.
 


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