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.

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.

Inhibikase Therapeutics to Present at Sachs 4th Annual Neuroscience Innovation Forum

On April 21, 2021 Inhibikase Therapeutics, Inc. (Nasdaq: IKT) (Inhibikase), a clinical-stage pharmaceutical company developing therapeutics to modify the course of Parkinson’s disease and related disorders inside and outside of the brain, reported that Milton Werner, Ph.D., President and Chief Executive Officer, will provide an update on clinical measures of dosing pharmacokinetics and elaborate on IKT-148009’s mechanism of action at the Sachs 4th Annual Neuroscience Innovation Forum being held virtually on April 28-30, 2021 (Press release, Inhibikase Therapeutics, APR 21, 2021, View Source [SID1234578320]).

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Dr. Werner will provide a corporate presentation, as well as participate in the Parkinson’s & Movement Disorders panel discussion on Wednesday, April 28th, at 1:20 p.m. ET. In addition, Dr. Werner will separately present a corporate overview of Inhibikase.

Mount Sinai Hospital in New York joins RhoVac’s Phase IIb Study in Prostate Cancer

On April 21, 2021 RhoVac AB ("RhoVac"), a Swedish cancer immunotherapy company, reported, April 21st 2021, that the prestigious Mount Sinai hospital in New York is initiated as the latest addition to US trial centres in RhoVac’s clinical phase IIb study, "BRaVac", in prostate cancer (Press release, RhoVac, APR 21, 2021, View Source [SID1234578319]).

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Mount Sinai Hospital, founded in 1852, is one of the oldest and largest teaching hospitals in the United States, and it is widely recognised and one of the leading hospitals in the US, and indeed in the world, and as such RhoVac is extremely proud to declare its participation in the BRaVac trial.

The participation of Mount Sinai was directly caused by the FDA approval of RhoVac’s Fast Track Designation. Immediately after the news on the Fast Track Designation was made public, Mount Sinai contacted RhoVac via its Scientific Advisory Board member, Professor Per-Anders Abrahamsson, who brokered the connection to RhoVac management. It is an honour for RhoVac, and a recognition of the potential of its drug candidate, that such a world leading hospital spontaneously seeks to join its clinical trial.

The site initiation visit is held, today, April 21st , and the study will be supervised at Mount Sinai by Professor Ash Tewari. In the trial, RhoVac’s drug candidate, RV001, will be used in prostate cancer patients that have previously had a prostatectomy or definitive radiation therapy, but that now have suffered a "Biochemical Recurrence" (rising PSA) but who still have not developed detectable metastases. The objective of the development of RV001 is to prevent/delay the recurrence of cancer and its progression to a metastatic state. If a clinical proof of concept is obtained in prostate cancer, several other cancer indications would also be candidates for development.

RhoVac CEO, Anders Månsson, comments: "I was of course delighted when I learned that Mount Sinai wanted to join our study. I regard this as yet another example of the recognition that the Fast Track Designation has brought us already, and I am happy that we could get started so quickly. I wish Mount Sinai welcome on board the trial team, and I look forward to our collaboration".

Ampio Pharmaceuticals, Inc. to Report Fiscal 2021 First Quarter Financial Results and Provide Corporate Business Update

On April 21, 2021 Ampio Pharmaceuticals (NYSE American: AMPE), a biopharmaceutical company focused on the advancement of immunology-based therapies for prevalent inflammatory conditions, reported it will host a conference call to discuss financial results for the quarter ended March 31, 2021 and provide a corporate business update on Wednesday, May 5, 2021 at 4:30pm EDT/ 2:30pm MT (Press release, Ampio, APR 21, 2021, View Source [SID1234578318]).

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The conference call will also be available from the Investor Relations section of the Company’s website at www.ampiopharma.com and will be archived there shortly after the live event.