Ionis to hold first quarter 2021 financial results webcast

On April 21, 2021 Ionis Pharmaceuticals, Inc. (NASDAQ: IONS) reported that it will host a live webcast on Wednesday, May 5th at 11:30 a.m. Eastern Time to discuss its first quarter 2021 financial results and report on pipeline and business progress (Press release, Ionis Pharmaceuticals, APR 21, 2021, View Source [SID1234578321]).

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Interested parties may access the webcast at View Source A webcast replay will be available for a limited time at the same address.

Vaccinex Announces Publication of Results from CLASSICAL-Lung Phase 1b/2 Clinical Trial in Non-Small Cell Lung Cancer in the Peer-Reviewed Journal Clinical Cancer Research

On April 21, 2021 Vaccinex, Inc. (Nasdaq: VCNX), a clinical-stage biotechnology company pioneering a differentiated approach to treating cancer and neurodegenerative disease through the inhibition of SEMA4D, reported the publication of results from the company’s CLASSICAL-Lung clinical trial in the journal Clinical Cancer Research, a publication of the American Association for Cancer Research (AACR) (Free AACR Whitepaper) (Press release, Vaccinex, APR 21, 2021, View Source [SID1234578306]). CLASSICAL-Lung was a Phase 1b/2 trial evaluating the company’s lead clinical candidate, pepinemab, in combination with the immune checkpoint inhibitor BAVENCIO (avelumab) for the treatment of non-small cell lung cancer (NSCLC).

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The paper, entitled, "A Phase 1b/2 Study of Pepinemab in Combination with Avelumab in Advanced Non-Small Cell Lung Cancer," presents data showing that pepinemab is clinically active when combined with BAVENCIO and was well tolerated, with no identified safety concerns. The combination appeared to halt or reverse tumor progression (partial response or stable disease) in a subset of both immunotherapy naïve patients, including patients with often difficult to treat PD-L1–negative or PD-L1–low tumors, and some patients with primary or acquired resistance to prior single-agent anti-PD-1/L1 therapy.

Among 21 evaluable immunotherapy naïve patients, most of whom had negative or low tumoral expression of the PD-L1 biomarker, five patients experienced partial responses, four patients evidenced clinical benefit at or greater than one year, and the disease control rate (DCR) was 81%. Notably, the objective response rate (ORR) with the combination therapy was higher than previously reported for single agent avelumab in the PD-L1 negative / low population. Among 29 evaluable patients who previously experienced disease progression during or following anti-PD-1/L1 immunotherapy, the subsequent combination treatment resulted in a DCR of 59%, including two partial responses and seven patients with durable clinical benefit of at least 23 weeks. Finally, exploratory biomarker analysis from biopsies demonstrated improved penetration of killer CD8+ T cells into the tumor.

Dr. Maurice Zauderer, President and CEO of Vaccinex, stated, "The results of the CLASSICAL-Lung study support our hypothesis that adding pepinemab to a checkpoint inhibitor for the treatment of NSCLC can shift the tumor microenvironment toward anti-tumor immunity and away from immunosuppression. This appears to enhance the efficacy of checkpoint inhibition, even in some patients who did not respond to prior anti-PD-1/L1 therapies. We are very pleased to have the full data set published in this prestigious peer-reviewed medical journal and look forward to the continued development of this promising combination for the treatment of NSCLC. We are particularly pleased to shortly begin a new study of the combination of pepinemab and Keytruda (pembrolizumab) in front-line Head & Neck cancer."

The publication is now available electronically at: View Source

About the CLASSICAL – Lung Clinical Trial

The design of the trial consisted of a 12-subject dose escalation phase to determine the recommended Phase 2 dose of pepinemab in combination with avelumab, followed by a 50-subject dose expansion phase. The study included a total of 21 evaluable patients who were immunotherapy naïve and 32 patients who were refractory or resistant to prior treatment with immune checkpoint inhibitors (predominantly anti–PD-1). The primary objective was to assess safety and tolerability. Secondary objectives included evaluation of efficacy, immunogenicity, and PK/PD. An exploratory objective was to identify candidate biomarkers of activity.

Roswell Park, Wilmot Cancer Institute Collaborate on First Large Study of Immunotherapy in Black Cancer Patients

On April 21, 2021 Roswell Park Cancer Institute reported A new collaboration between two Western New York cancer research leaders will help oncologists learn whether Black and white cancer patients respond differently to a game-changing immunotherapy treatment, and seeks to improve the safety and effectiveness of these newer drugs in diverse populations (Press release, Roswell Park Cancer Institute, APR 21, 2021, View Source [SID1234578322]).

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Funded by a two-year, $2.08 million grant from the National Cancer Institute (NCI), with the possibility of additional funding after the initial phase of study concludes, Roswell Park Comprehensive Cancer Center and the University of Rochester’s Wilmot Cancer Institute are working together to fill a major gap in the science around immune checkpoint inhibitors (ICIs).

Direct Cohort
Checkpoint inhibitors — such as nivolumab (Opdivo) and pembrolizumab (Keytruda) — have become standard care for 16 different types of cancer, both early and advanced-stage. They work by blocking signals in the immune system, clearing a path for the body’s natural T cells to kill cancer. Since their approval in 2011, the use of these drugs has skyrocketed and is believed to be partly responsible for a significant drop in U.S. cancer deaths.

Still, there are many opportunities to improve the care of patients who may benefit from ICIs. For example, few people of African ancestry participated in the original clinical trials to evaluate these treatments. The Roswell Park-Wilmot collaborators plan to collect data that will allow them to investigate side effects, toxicities and outcomes among people of African ancestry who take immune checkpoint inhibitors.

The research builds off discoveries from Roswell Park that helped explain why standard treatments are often less effective in patients of African ancestry.

"Checkpoint inhibitors have largely not been studied in Black cancer patients, but our recent findings show that there may be a particular benefit to these immunotherapies for cancer patients of African ancestry — across a variety of cancer types," says Christine Ambrosone, PhD, Chair of Cancer Prevention & Control at Roswell Park and a Co-Investigator on the study.

"Because Black cancer patients tend to have a prevalence of what we call ‘exhausted,’ nonfunctional T cells, we realized they may be more likely to do well on immune checkpoint inhibitors, which target the exhausted T cells to revive them and restore their ability to fight cancer cells," says Song Yao, PhD, Professor of Oncology in Roswell Park’s Department of Cancer Prevention and Control, Co-Principal Investigator on the study. "But we can’t know this without further study, and this new project will tackle that knowledge gap in a large and diverse patient population."

The Wilmot team, under the leadership of Co-Principal Investigator Charles Kamen, PhD, MPH, and Co-Investigator Gary Morrow, PhD, MS, will leverage the center’s position as a hub for the National Community Oncology Research Program (NCORP). Dr. Morrow, a Dean’s Professor of Surgery at the University of Rochester Medical Center, is co-Principal Investigator for the NCORP program, which is supported by a $29 million NCI grant. The NCORP network will allow the researchers to carry out the immune checkpoint study at hundreds of community oncology clinics in the NCORP network across the country. The team also plans to enroll study participants in Western New York.

"Our project is designed to get the full 360 picture of Black patients who receive immunotherapy," says Dr. Kamen. "Not only are we measuring their response to treatment, but we’re also looking at factors like discrimination by providers and health care systems and how often treatment is stopped, so that we have a better understand of equity and access to high-quality care."

The Roswell-Wilmot collaborators have designed a large national study — known as the DiRECT Cohort — that will seek to enlist 600 Black patient volunteers and 1,200 white cancer patients of European ancestry.

Dr. Gary Morrow
Dr. Gary Morrow
"The National Cancer Institute Community Oncology Research Program (NCORP) Research Base we have had at Wilmot for three decades is ideally suited to help direct a large nationwide study like this," said Dr. Morrow. "We’re eager and proud to actively participate in this important research with our longtime colleagues and friends from Roswell."

The project is the first large, national study of diverse patients treated with ICIs.

The researchers will conduct genetic analyses, for example, of the percent African ancestry in each Black patient, as well as social determinants of health, such as access to healthcare, as a predictor of treatment response and toxicities. In addition, they will evaluate how often treatment delays occur among the Black and white patients due to severe side effects, and the short- and long-term treatment outcomes.

Cancer patients at member sites within the Roswell Park Care Network will have access to the study through the participation of study Co-Investigator Igor Puzanov, MD, MSCI, FACP, Senior Vice President of Clinical Investigation at Roswell Park.

The new funds are in addition to the $5.2 million awarded to Roswell Park last year to study these dynamics using data reported to the New York State Cancer Registry.

Genprex to Participate in CEO Roadshow Webinar Series

On April 21, 2021 Genprex, Inc. ("Genprex" or the "Company") (NASDAQ: GNPX), a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, reported that its President and Chief Executive Officer, Rodney Varner, will be participating in a webinar series with CEO Roadshow to provide a company overview to investors on a weekly basis from April 22 through June 10, 2021 (Press release, Genprex, APR 21, 2021, View Source [SID1234578307]).

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Details for the weekly CEO Roadshow webinar series:

Host: CEO Roadshow

Date: Once per week, each Thursday, from April 22 through June 10, 2021

Time: Thursdays from 11-11:30 a.m. EDT

Webinar Link: https://bit.ly/3eoHeie

Mr. Varner will be available for questions following each company presentation. The webinars will be recorded and available for replay on Genprex’s website for a period of time. Replays will also be available on CEORoadshow.com following each webinar. The CEO Roadshow webinar series features small and mid-cap stocks that are on the verge of a breakout or have other near-term developments making them an attractive long-term investment opportunity.

Sermonix Pharmaceuticals Project With Huntsman Cancer Institute Researcher to Investigate Potential Effects of Lasofoxifene on ESR1 Mutations in Endometrial Cancer

On April 21, 2021 Sermonix Pharmaceuticals Inc., a privately held biopharmaceutical company developing innovative therapeutics to treat ESR1-mutated metastatic breast and gynecological cancers, reported a preclinical collaboration with researcher Jay Gertz, Ph.D., to examine the potential effects of lasofoxifene, Sermonix’s lead investigational drug, on endometrial cancer (Press release, Sermonix Pharmaceuticals, APR 21, 2021, View Source [SID1234578341]).

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The project will investigate the effects of lasofoxifene on unique models of endometrial cancer that carry ESR1 mutations. Lasofoxifene has shown novel activity in ESR1 mutations, and Sermonix is currently enrolling patients in two Phase 2 Evaluation of Lasofoxifene in ESR1 Mutations (ELAINE) studies within the breast cancer arena.

"Sermonix is committed to exploring ESR1 mutations across gynecological tumor types and examining lasofoxifene’s potential to serve the unmet medical needs of more women fighting cancer," said Barry Komm, Ph.D., chief scientific officer of Sermonix. "The unique ESR1 model system is state-of-the-art for this exploration and Dr. Gertz is an esteemed partner with whom it is an honor for Sermonix to collaborate."

Dr. Gertz is a cancer researcher at Huntsman Cancer Institute and associate professor of oncological sciences at the University of Utah. His lab studies how transcription regulation is altered in cancer with a particular focus on the roles of steroid hormone signaling in endometrial and breast cancers.

"The Gertz Lab has a major emphasis in advancing the study of new drugs for endometrial cancer, an aggressive disease with limited treatment options," said Dr. Gertz. "We look forward to learning more about the efficacy of lasofoxifene in the context of ESR1-mutated endometrial cancer."

About Lasofoxifene
Lasofoxifene is an investigational, nonsteroidal selective estrogen receptor modulator (SERM), which Sermonix licensed globally from Ligand Pharmaceuticals Inc. (NASDAQ: LGND) and has been studied in previous comprehensive Phase 1-3 non-oncology clinical trials in more than 15,000 postmenopausal women worldwide. Lasofoxifene’s bioavailability and activity in mutations of the estrogen receptor could potentially hold promise for patients who have acquired endocrine resistance due to ESR1 mutations, a common finding in the metastatic setting and an area of high unmet medical need. Lasofoxifene’s novel activity in ESR1 mutations was discovered at Duke University and Sermonix has exclusive rights to develop and commercialize the product in this area. Lasofoxifene, a potent, oral SERM could, if approved, play a critical role in the targeted precision medicine treatment of advanced ER+ breast cancer.