Promedior Innately Superior Therapeutics for Fibrosis
 

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See our novel approach to fibrosis

Promedior is a clinical stage biotechnology company developing novel therapeutics for the treatment of fibrosis.

Fibrosis is the harmful build-up of scar tissue leading to loss of tissue and organ function. The fibrosis pathology is the hallmark of a number of rare diseases, such as Myelofibrosis, Scleroderma, and Idiopathic Pulmonary Fibrosis, and is a common complication of diabetes including diabetic nephropathy, diabetic retinopathy, and NASH Syndrome, as well as a feature common in many other chronic inflammatory or infectious diseases.  These fibroproliferative diseases are a leading cause of death and disability, and there are currently no approved therapies that can arrest or reverse the fibrosis process.

Promedior is pioneering the development of targeted therapeutics to treat fibroproliferative diseases by regulating the innate immune system’s response to injury.   Promedior’s drug candidates are based on Pentraxin-2, an endogenous human protein that regulates the differentiation of monocyte-lineage cells that control the fibrosis cascade.  The company has extensive research validation of its therapeutic approach with pentraxins and is progressing in human clinical trials.

While the range of potential clinical indications in the fibrosis field is broad, Promedior is focusing its product development in two areas: rare systemic fibrotic diseases such as Myelofibrosis and Idiopathic Pulmonary Fibrosis, and fibrovascular retinal diseases such as age-related macular degeneration (AMD), diabetic retinopathy, and proliferative vitreoretinopathy (PVR).  Promedior is exploring corporate partnerships in some of the larger market indications for fibrosis-related diseases.

 
 

News & Events

May 15, 2012
Promedior Appoints Suzanne L. Bruhn, Ph.D., as President and Chief Executive Officer

May 7, 2012
Promedior Announces Presentation of Preclinical Data at ARVO Demonstrating that Pentraxin-2 Suppressed Fibrosis, Neovascularization, and Vascular Leakage

March 7, 2012
Promedior Secures $21.5 Million in First Closing of Series D Financing to Expand and Advance Pipeline of Pentraxin-2 Therapeutics for Fibrotic Diseases

March 7, 2012
Promedior Receives U.S. Orphan Drug Designation for PRM-151 for the Treatment of Idiopathic Pulmonary Fibrosis (IPF)

Publication
Santhiago MR, et al. (2011) Monocyte development inhibitor PRM-151 decreases corneal myofibroblast generation in rabbits. Experimental Eye Research Sep 14.

November 7, 2011
Promedior Presents Preclinical Data at AASLD Demonstrating That Pentraxin-2 Suppresses Liver Fibrosis and Has a Clear Hepatoprotective Effect

May 16, 2011
Promedior Presents Clinical Data for PRM-151 (rhPTX-2) in Idiopathic Pulmonary Fibrosis at American Thoracic Society 2011

May 4, 2011
Promedior Announces Presentation of Preclinical Data at ARVO Demonstrating PRM-151 (rhPTX-2) Reduces Neovascularization in Retinal Diseases


 
   
 

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