The Castleman Disease Collaborative Network Announces a Research Collaboration with Janssen to Conduct a Proteomics Study of Idiopathic Multicentric Castleman Disease

PHILADELPHIA--()--The Castleman Disease Collaborative Network (CDCN), a global non-profit organization dedicated to accelerating research and treatments for Castleman disease (CD), a rare immunological disease, announced today a collaboration with Janssen Research & Development, LLC, to conduct a proteomics study of idiopathic multicentric Castleman disease (iMCD), a deadly subtype of CD. This collaborative study has the potential to improve diagnosis and treatment for iMCD patients. The collaboration combines CDCN’s strong expertise in iMCD research and its world-wide network of physician researchers with Janssen’s industry leading iMCD research resources.

“Ever since I was diagnosed with iMCD ten years ago, I have been dedicated to doing whatever I can to improve CD research and awareness. We have made progress, but have important work ahead of us to understand the causes of CD, and develop diagnostic tests and treatments for it”

The causes of iMCD, one of three subtypes of CD, are unknown. About 1,0001 new cases of iMCD are diagnosed each year in the United States and approximately 35% of patients die within five years of diagnosis2. iMCD patients experience a wide spectrum of symptoms, from mild flu-like symptoms to acute sepsis-like multiple organ system failure due to uncontrolled immune system activation. Siltuximab, an anti-interleukin-6 monoclonal antibody developed by Janssen, was approved by the U.S. Food and Drug Administration for treatment of iMCD in 2014. However, many questions still exist related to iMCD, particularly for patients that do not respond to siltuximab.

“Ever since I was diagnosed with iMCD ten years ago, I have been dedicated to doing whatever I can to improve CD research and awareness. We have made progress, but have important work ahead of us to understand the causes of CD, and develop diagnostic tests and treatments for it,” stated, Greg Pacheco, Board President of CDCN.

Recently, CDCN brought together a team of physicians and researchers to establish the first-ever diagnostic criteria for iMCD, which was published last month in the journal, Blood. These criteria include clinical and pathology features, and diseases to exclude. However, the diagnostic process can be time-consuming as there is no definitive test for iMCD. Therefore, the aim of this study is to identify molecules whose levels are specifically altered in the blood of iMCD patients. The hope is that these molecules can be used to shorten the time required to diagnose iMCD for critically ill patients and as therapeutic targets for treatment of iMCD patients that do not respond to current therapies. To accomplish these goals, the collaborators will measure the level of approximately 1,300 analytes in more than 260 serum samples collected from approximately 100 iMCD patients at various time points during active disease.

This unprecedented collaboration reflects a trend towards greater collaboration between industry, research foundations, and academia, as well as continued interest in drug development for rare diseases. Janssen will fund a significant portion of the project and contribute iMCD serum samples that were collected as part of a previous clinical trial. CDCN’s role in the collaboration includes, through its network of physician scientists, partnering with seven academic institutes from around the globe to contribute iMCD, related disease and ‘normal’ serum samples and analyzing the results of the proteomic screen. CDCN will also fund a portion of the project.

“It is unusual and creative for a pharmaceutical company to open up their banks of samples for research and to do it in such a collaborative fashion. Janssen’s commitment to fully leveraging its iMCD resources to advance high-impact, patient-centric research demonstrates its commitment to helping patients,” stated Pacheco. “The results of this ambitious research project have the potential to shed significant light on a poorly understood disease and improve survival for all CD patients.”

About Castleman Disease Collaborative Network (CDCN)

CDCN is a global initiative dedicated to accelerating research and treatment for Castleman disease (CD) to improve survival for all patients with CD. The CDCN’s innovative approach first involved building a global community of over 400 physicians and researchers, assembling a scientific advisory board of 28 experts from eight countries, and supporting and engaging patients in research prioritization. Then, the CDCN crowdsourced among the global community to identify gaps in medical knowledge and determine high priority research projects. In parallel, the CDCN connects and supports thousands of CD patients around the world. Now, the CDCN recruits top researchers to conduct studies, and works with patients, loved ones, and the public to raise funding to enable these studies. More information is available at: www.CDCN.org

1. Munshi et al. Leukemia & Lymphoma
2. Dispenzieri et al. American Journal of Hematology

Contacts

Castleman Disease Collaborative Network (CDCN)
Greta Moretto, 610-304-0696
greta@castlemannetwork.org
or
Alisa McDonald, 610-304-0696
alisa@castlemannetwork.org

Release Summary

Castleman Disease Collaborative Network Announces a Research Collaboration with Janssen to Conduct a Proteomics Study of Idiopathic Multicentric Castleman Disease

Castleman Disease Collaborative Network (CDCN)