Autoimmunity BioSolutions Enhances Leadership to Advance Innovative Therapeutics
Autoimmunity BioSolutions Enhances Leadership to Advance Innovative Therapeutics
Autoimmunity BioSolutions (ABS) has taken a significant step forward in its commitment to advancing treatments for autoimmune diseases. Recently, the company announced key appointments to its leadership team, which will play a critical role in driving its innovative, personalized, genetically guided immuno-corrective therapy. This therapy targets elevated levels of soluble IL7 receptor (sIL7R), a crucial factor contributing to poor responses to traditional treatments.
Strengthening the Leadership Team
The company appointed Dr. Richard Polisson as the Chief Medical Officer and Jen Beachell as the Chief Business Officer. Dr. Polisson brings extensive experience as a former Senior Vice President at Sanofi-Genzyme, where he led various developmental programs in immune-mediated diseases. His expertise in rheumatology and experience at prestigious institutions such as Mass General Hospital and Harvard Medical School positions him well to steer the clinical aspects of ABS's offerings.
Jen Beachell, known for her role as the founding Chief Commercial and Chief Operating Officer of Upstream Bio, also joins the team with a wealth of experience in the pharmaceutical industry. Having previously led commercial strategies at Johnson and Johnson, Beachell's insight and knowledge in the autoimmunity domain will greatly benefit ABS as it embarks on its next phase of growth.
Addressing Unmet Needs in Autoimmune Disease Treatments
The firm is on a mission to fill a critical gap in the treatment of autoimmune diseases, addressing the alarming rates of non-response to current therapies. Data shows that approximately 50% of patients suffering from diseases like rheumatoid arthritis, lupus nephritis, and type 1 diabetes do not achieve satisfactory outcomes with standard care. This is partially attributed to elevated levels of sIL7R, which ABS aims to normalize through its innovative therapy.
ABS's research has identified a common single nucleotide polymorphism (SNP) that significantly impacts the levels of sIL7R, providing a genetic basis for poor therapeutic responses. The company is positioned to explore solutions that will enhance the effectiveness of existing treatments for these conditions, suggesting that the normalization of sIL7R could remarkably improve patient outcomes.
A Strategic Development Pathway for Clinical Success
To realize its ambitious goals, ABS plans to initiate patient bio-sample studies, starting with rheumatoid arthritis and subsequently expanding to investigate lupus/lupus nephritis and type 1 diabetes. By closely monitoring the response of patients on standard treatments while measuring the genetic factors influencing their outcomes, ABS aims to establish a direct correlation between these factors and treatment efficacy. With a robust biostatistical model, the company seeks to conduct Proof-of-Concept (POC) studies that promise to revolutionize treatment strategies tailored to genetically predisposed populations.
The strategic design of these studies will allow ABS to compare the standard-of-care treatments against their novel therapy, which aims to reduce sIL7R levels. This model mirrors successful clinical trial designs previously used in the industry, which have paved the way for drug approvals.
Looking Ahead
With these leadership changes and a clear roadmap laid out, Autoimmunity BioSolutions is well-equipped to confront the challenges faced in autoimmune disease management. Through its dedication to personalized care and innovative research, ABS is poised to make a significant impact on patient lives.
As stated by CEO Gene Williams, the expansive experience of the new leadership team positions ABS not only to thrive as a company but also to make meaningful progress in delivering personalized therapies that accurately meet patient requirements. This commitment could very well usher in a new era of targeted treatments for those who have long struggled with inadequate responses to existing therapies, offering hope for a brighter future in autoimmune disease treatment.