WESTCHESTER COUNTY LIFE SCIENCES UPDATE

Featuring news, events and industry trends

Regeneron and Sanofi Present Positive Results from Clinical Trial Assessing Drug for Moderate-to-Severe

Atopic Hand and Foot Dermatitis


Tarrytown’s Regeneron Pharmaceuticals, Inc. and Sanofi presented positive results from the clinical trial assessing Dupixent® (dupilumab) in adults and adolescents with uncontrolled moderate-to-severe atopic hand and foot dermatitis. The trial, the first evaluating a biologic for this difficult-to-treat population, met its primary and key secondary endpoints. The results were featured in a late-breaking session, one of more than 20 Dupixent scientific presentations, at the American Academy of Dermatology (AAD) 2023 Annual Meeting.


There are 23 Dupixent scientific abstracts being presented across three dermatological diseases with underlying type 2 inflammation at the AAD 2023 Annual Meeting. These include oral presentations on long-term Dupixent use in children as young as 6 months with atopic dermatitis; the impact of Dupixent treatment on health-related quality of life, skin pain and sleep in prurigo nodularis; and the investigational use of Dupixent on signs, symptoms and health-related quality of life in chronic spontaneous urticaria.

 

The potential use of Dupixent in chronic spontaneous urticaria is currently under clinical development, and the safety and efficacy have not been fully evaluated by any regulatory authority.


Drug Demonstrates Potential to Become First Biologic to Treat COPD By Showing Significant Reduction in Exacerbations in Pivotal trial

 

Tarrytown headquartered Regeneron Pharmaceuticals, Inc. and Sanofi announced the primary and all key secondary endpoints were met in a Phase 3 trial evaluating the investigational use of Dupixent® (dupilumab) compared to placebo in adults currently on maximal standard-of-care inhaled therapy (triple therapy) with uncontrolled chronic obstructive pulmonary disease (COPD) and evidence of type 2 inflammation. Dupixent is the first and only biologic to demonstrate a clinically meaningful and highly significant reduction (30%) in moderate or severe acute exacerbations of COPD (rapid and acute worsening of respiratory symptoms) over 52 weeks, while also demonstrating significant improvements in lung function, quality of life and COPD respiratory symptoms.

 

COPD is a life-threatening respiratory disease that damages the lungs and causes progressive lung function decline. Symptoms include persistent cough and breathlessness that may not only impair the ability to perform routine daily activities, but can also lead to anxiety, depression and sleep disturbances. COPD is also associated with a significant health and economic burden due to recurrent acute exacerbations that require systemic corticosteroid treatment and/or lead to hospitalization or even death. Smoking is a key risk factor for COPD, but even individuals who quit smoking can still develop the disease. In the U.S. alone, approximately 300,000 people live with uncontrolled COPD with type 2 inflammation.

 Leukemia & Lymphoma Society Announces

E. Anders Kolb, M.D., as New President & CEO

 

The Leukemia & Lymphoma Society (LLS), headquartered in Rye Brooke, has announced E. Anders Kolb, M.D., as its new President and Chief Executive Officer (CEO). He will join LLS on May 1, 2023, succeeding Louis J. DeGennaro, Ph.D., who has led the organization since 2014 and retires on June 30, 2023.


In his new role, Dr. Kolb will lead the $500 million organization in its mission to cure leukemia, lymphoma, Hodgkin's disease and myeloma, and improve the quality of life for blood cancer patients and their families. He is joining the only cancer and healthcare organization in the not-for-profit category that made Fast Company's 2022 Brands that Matter List. An organization with a Four-Star Rating from Charity Navigator, and the only superior ranking in Cause Reports latest analysis of eight of the largest chronic disease organizations.

Cognition Therapeutics to Present Analyses from Clinical Studies of CT1812 in Patients with Alzheimer’s Disease

at AD/PD 2023


Purchase's Cognition Therapeutics, Inc. will be presenting results of a proteomic biomarker meta-analysis of cerebrospinal fluid, or CSF, samples from the initial cohort of participants in the Phase 2 SHINE and Phase 1b SPARC studies with mild-to-moderate Alzheimer's disease who were treated with either CT1812 or placebo. Results of this analysis identified biomarkers of CT1812 activity that replicated across these two independent studies and patient cohorts. These findings inform our understanding of the impact of CT1812 treatment on the network of biologic pathways associated with Alzheimer’s disease progression. A detailed poster presentation (poster #P0407) will be made at the upcoming AD/PD™ 2023: the International Conference on Alzheimer’s & Parkinson’s Diseases being held in Gothenburg, Sweden from March 28 to April 1, 2023.


In addition, Lisa Ricciardi, CEO of Cognition Therapeutics, will be participating in a panel hosted by the Alzheimer’s Drug Discovery Foundation. The panel, “Emerging Solutions: Novel Approaches to Alzheimer’s Disease” will take place in the Industry Symposium, “Building the Future: Novel Approaches and Innovations in Alzheimer’s Research" being held on March 29, 2023 at 11:40am local time. The panelists will discuss the need for multiple novel approaches to address neurodegenerative diseases with an emphasis on the value of rigorous and biomarker-driven clinical trials to help implement this multipronged approach.


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