Celldex Therapeutics Shares Exciting Study Results in CSU Treatment
Celldex Therapeutics Announces Groundbreaking Results
Celldex Therapeutics, Inc. recently revealed that an abstract detailing 52-week results from its Phase 2 clinical trial of barzolvolimab in patients suffering from chronic spontaneous urticaria (CSU) has been accepted for a late-breaking oral presentation. The presentation will occur at the European Academy of Dermatology and Venereology (EADV) Congress 2024, set to take place in Amsterdam.
Details on the Presentation
This exciting development highlights the company's ongoing commitment to addressing significant challenges faced by patients with CSU, especially those who do not respond to conventional antihistamines. The session scheduled for Wednesday is anticipated to captivate attendees interested in recent advancements in dermatology and allergy treatment.
The abstract presented at the event will focus on the profound efficacy and safety of barzolvolimab demonstrated over the 52-week trial period. This is a notable breakthrough for patients who experience severe symptoms despite existing treatment options.
Presentation Information
Here are some essential details about the upcoming presentation:
- Abstract Title: Barzolvolimab shows profound efficacy and favorable safety over 52 weeks in patients with Chronic Spontaneous Urticaria
- Presenting Author: Martin Metz, M.D., a distinguished professor of dermatology and allergy
- Session: D1T01.2: Late breaking news
- Date/Time: Wednesday, September 25 at 16:45-17:00 CEST (10:45 – 11:00 am ET)
E-Poster Presentation
In addition to the oral presentation, Celldex will also present an e-Poster (#P3596) titled "Barzolvolimab treatment improves quality of life and urticaria control in patients with chronic spontaneous urticaria (CSU): Results from a Phase 2 trial." This presentation will shed light on how patients managed their symptoms and improved their quality of life following the treatment.
The Significance of Barzolvolimab
Barzolvolimab, sometimes referred to as CDX-0159, represents an innovative approach to treating CSU by targeting mast cell biology. This methodology has the potential to revolutionize treatment protocols for patients dealing with chronic allergies, autoimmune disorders, and other serious inflammatory conditions. Additionally, the emphasis on safety during the lengthy trial indicates Celldex's strong dedication to patient well-being.
About Celldex Therapeutics
Celldex Therapeutics is a pioneering clinical-stage biotechnology firm dedicated to developing therapies that harmonize with the human immune system. The company's focus lies in creating therapeutics derived from antibodies that significantly impact critical pathways involved in immune responses, promising hope for patients with severe allergies and autoimmune diseases.
Commitment to Innovation
As a company, Celldex embodies the spirit of innovation with a robust pipeline of potential therapy candidates. The ongoing dedication to enhancing therapeutic efficacy showcases their proactive approach in the field of biotechnology.
Company Contact Information
For inquiries, please reach out to:
Sarah Cavanaugh
Senior Vice President, Corporate Affairs & Administration
(508) 864-8337
scavanaugh@celldex.com
Patrick Till
Meru Advisors
(484) 788-8560
ptill@meruadvisors.com
Frequently Asked Questions
What is the focus of Celldex's upcoming presentation?
Celldex will present the results of a Phase 2 trial for its treatment, barzolvolimab, aimed at chronic spontaneous urticaria.
Where will the EADV Congress take place?
The EADV Congress will be held in Amsterdam.
What does the trial results indicate about barzolvolimab?
The trial results suggest that barzolvolimab provides significant efficacy and has a favorable safety profile for treating chronic spontaneous urticaria.
Who is presenting the study findings?
The findings will be presented by Martin Metz, M.D., a professor in dermatology and allergy.
How can I learn more about Celldex Therapeutics?
Further information can be found on their official website or by contacting the company directly via their listed email addresses.
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