Agenus Stock Price, News & Analysis

Agenus (NASDAQ: AGEN) will release its Q1 2022 financial results on May 10, 2022, before market opening. The company focuses on immuno-oncology, developing therapies that leverage the immune system against cancer. A conference call and webcast are scheduled for the same day at 8:30 a.m. ET to discuss results and offer a corporate update. The call can be accessed via dial-in numbers provided, and a replay will be available on the company's website. For more information, visit www.agenusbio.com.

Agenus Inc. (Nasdaq: AGEN) announced preclinical data presentation of AGEN1571, a novel anti-ILT2 antibody, at the AACR Annual Meeting on April 8-12, 2022. The data highlight robust adaptive and innate immune responses, showing AGEN1571's superior performance compared to existing clinical-stage competitors. Key findings include a ~10-fold higher binding affinity and complete blockade of ILT2-ligand interactions. The company has cleared its Investigational New Drug (IND) application, paving the way for upcoming clinical trials, further enhancing its immuno-oncology pipeline.

Agenus Inc. (NASDAQ: AGEN) received a $5M clinical milestone payment for AGEN2373, a CD137 agonist, as part of its ongoing Phase 1b study in melanoma patients resistant to prior anti-PD-1 therapy. The combination of AGEN2373 and botensilimab has shown promising preclinical results, boosting tumor control. AGEN2373 is well tolerated, with no liver toxicity reported. Gilead holds an exclusive option to license AGEN2373, while Agenus can opt-in to share development costs, allowing for a potential 50:50 profit split and co-commercialization in the U.S.

Agenus (NASDAQ: AGEN) announced a collaboration with Targovax to develop TG mutant KRAS cancer vaccines combined with Agenus’s QS-21 STIMULON adjuvant. This partnership may lead to an exclusive commercial agreement based on successful clinical trial outcomes. The TG vaccines target mutations in the RAS gene, responsible for approximately 30% of cancers. Targovax has received significant funding to advance the TG program, while QS-21 STIMULON is recognized for its effectiveness in boosting immune responses. Positive clinical results could yield tiered royalties for Agenus.

Agenus Inc. (NASDAQ: AGEN) reported its 2021 financial results, ending with $307 million in cash. The company advanced key clinical programs, notably botensilimab, which has shown promise in treating multiple cold, treatment-resistant cancers. Phase II studies are set to begin for melanoma, MSS-colorectal, and pancreatic cancers, aiming to outperform traditional therapies. Revenue surged to $296 million in 2021, driven by license fees and milestone payments, despite a net loss of $29 million. The firm is strategically positioned for future growth, backed by significant partnerships and proprietary technology.

Agenus (NASDAQ: AGEN) will announce its fourth quarter and full year 2021 financial results before the market opens on March 1, 2022. A conference call will follow at 8:30 a.m. ET, where executives will discuss the financial outcomes and provide a corporate update. Investors are encouraged to participate via dial-in or webcast. The company is focused on advancing immuno-oncology therapies and has a robust pipeline supported by state-of-the-art manufacturing capabilities. Further details can be found on their website.

Agenus (NASDAQ: AGEN), a clinical-stage immuno-oncology company, announced its participation in two investor conferences. The H.C. Wainwright Bioconnect Conference will feature an on-demand presentation starting January 10, 2022. Additionally, they will present at the B. Riley Securities’ 2022 Virtual Oncology Conference on January 27, 2022, at 1:00 PM EST. Investors can access webcasts and replays on the company's website. Agenus focuses on developing therapies that utilize the immune system to combat cancer and has a robust pipeline of treatments.

Agenus (NASDAQ: AGEN) reported positive results from a Phase 2 clinical study of the combination therapy balstilimab and zalifrelimab for patients with recurrent/metastatic cervical cancer. The objective response rate (ORR) reached 32.8% in PD-L1-positive patients and 25.6% overall, significantly outperforming existing treatments. Notably, the median duration of response remains unachieved after 21 months of follow-up, indicating promising durability of response. The safety profile was well-tolerated, with no unexpected toxicities noted.

VBI Vaccines Inc. announced updated 12-month and 18-month overall survival data from its Phase 2a study of VBI-1901, a cancer vaccine targeting recurrent glioblastoma (GBM). The data showed a significant improvement in overall survival compared to historical controls, with some patients experiencing up to 93% tumor reduction. The company plans to expand the study to support an application for accelerated approval, with new trials anticipated in Q1 2022 for recurrent GBM and mid-2022 for primary GBM. These results suggest promising efficacy and a need for innovative therapies in GBM treatment.