Interview with Dupuytren’s Disease Patient and Company Founder

Early stage Dupuytren's disease - an immune-fibrotic disease of the hands
Bioworld’s Cormac Sheridan sits down with Kurt Harrington, CEO and Founder of Ventoux Biosciences to discuss his experience with and mission to transform Dupuytren’s treatment

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Ventoux Biosciences Takes Aim at Dupuytren’s Disease

Dupuytren’s disease is often referred to as “the most common crippling hand condition that people have never heard of,” but Kurt Harrington is on a mission to change that. A seasoned biotech and pharma consultant, Harrington has had the condition himself for over a decade and, acutely aware of the lack of available treatment options, has founded Ventoux Biosciences Inc. to bring additional therapies forward. His father also has Dupuytren’s disease and, as a father of two teenage boys who are at risk of developing the condition, Harrington is motivated to improve prospects for future patients. 

Also known as ‘Celtic hand’, Dupuytren’s mainly affects people of Northern European descent, although data for other ethnic groups are lacking. Genetic and environmental factors can contribute to the risk profile, but the inheritance is complex, involving multiple loci. One Dutch study published more than a decade ago identified six genes encoding Wnt pathway proteins, suggesting the involvement of that pathway in the pathology.

Disease Prevalence & Pathophysiology

It has a high prevalence – about 30 million people in the U.S. and Europe are affected, although not all would necessarily need treatment, Harrington told BioWorld, as the severity of the condition varies. Formally called palmar fibromatosis, the condition is characterized by the formation of fibrous nodules and cords, which, over time, can lock one or more fingers into a bent position and limit everyday movements and functions. It can be debilitating for those with severe disease. 

The pathophysiology is complex and not fully understood, but it has inflammatory as well as fibrotic dimensions. Some commentators believe it to be painless. “That is absolutely incorrect,” Harrington said. Over 30% of patients experience pain, he said. 

Surgery Remains the Mainstay of Treatment

Surgical intervention was for a long time the only option – and there are still no approved non-invasive therapies. Auxilium Pharmaceuticals, now part of Dublin-based Endo International plc, secured FDA approval in 2010 for Xiaflex (collagenase Clostridium histolyticum), which works by breaking down the collagen deposits that form in the palmar fascia or fibrous layer of tissue under the skin. It is still administered, Harrington said as part of a surgical procedure, however. “There’s really nothing for early to moderate patients,” he said.

Early stage patients are typically told to wait until their condition worsens before they can be considered eligible for treatment. Current treatment is not usually curative either – recurrence rates can be as high as 85%, and treatment complications are also frequent. Still less than 50 years, he has already undergone three hand surgeries and three courses of targeted radiation therapy.

Ventoux Bio’s Approach

San-Diego-based Ventoux is repurposing drugs that have already been in human trials – it will pursue a 505(b)2 regulatory pathway, which permits the use of data from studies conducted by third parties. It has two preclinical small-molecule programs underway, VEN-201 and VEN-202, with distinctive mechanisms, but it has yet to reveal any details. Preclinical data from a bleomycin-induced mouse model of the condition are imminent, and these will form the basis of pre-IND discussions with the FDA.

Harrington sees a role for new drugs both to slow progression of early stage disease but also to improve outcomes for more advanced patients undergoing surgery. There is a systemic dimension to the condition, too – he himself also experiences Ledderhose disease, or plantar fibromatosis, which affects the feet.

Xiaflex is also indicated for Peyronie’s disease, which is characterized by the build-up of a fibrotic plaque in the penis. It causes penile curvature and can make sex painful or impossible. These indications could also be options for its pipeline. Ultimately, Harrington said, Dupuytren’s could become a model indication for compounds targeting other fibrotic indications, given the accessibility of the hand and the rapid readout it can offer. 

180 Life Sciences Corp., of Palo Alto, Calif., is already in the clinic with a biosimilar version of the tumor necrosis factor alpha (TNF-alpha) inhibitor adalimumab. In a placebo-controlled phase IIb trial, monthly injections softened and reduced the size of the treated nodules. The study authors noted that both parameters continued to decline up to nine months after the fourth and final injection. “We’re all optimistically watching that one as well,” Harrington said.

Ventoux is currently self-funded, but Harrington plans shortly to raise finance and expand the leadership team. The company’s name is a nod to Harrington’s passion for cycling – Mont Ventoux is also known as ‘the beast of Provence’ and represents one of the most grueling climbs in the Tour de France. An accomplished guitar player and a triathlete to boot, Harrington does not shirk a challenge. This venture may be his biggest one yet.

©2023 BioWorld. Reprinted with permission from Clarivate.


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Johnny Randel

Johnny Randel is a senior finance executive who has more than 30 years of experience in financial institutions including over 17 in private equity.

Mr. Randel recently retired as the Chief Financial Officer (“CFO”) of StepStone Group. Inc (Nasdaq: STEP), a global private markets specialist firm delivering tailored investment solutions, advisory services, and impactful, data-driven insights to the world’s investors with $678B of capital responsibility. Mr. Randel spent over 13 years leading the corporate and investment finance and accounting teams and was the CFO for the lead up and execution of the company’s initial public offering in 2020.

Previously, Mr. Randel held the role of Chief Financial Officer and Chief Operating Officer at Citigroup Private Equity overseeing financial and operational activities for the company and its coinvestment, mezzanine, and fund of fund investment programs. Mr. Randel also held a previous role as Assistant Treasurer within Citigroup Inc.’s Treasury department where he managed rating agency relationships and fixed income client relations. Mr. Randel also held various finance roles supporting corporate finance and strategy over the course of his career. Mr. Randel received his B.G.S. from the University of Kansas and MBA from the University of Southern California.

Matt Cravets

Mr. Cravets is an industry leader in biostatistics with extensive experience in program design and analysis. He currently serves as the Senior Vice President of Biometrics at Gossamer Bio. Prior to joining Gossamer Bio, Mr. Cravets was Vice President of Biometrics at Heron Therapeutics Inc. from 2016 to 2018, where he played a key role in the late-stage development programs for Zynrelef for the treatment post-surgical pain and Cinvanti for the prevention of chemotherapy induced nausea and vomiting. Before joining Heron, Mr. Cravets was Executive Director of Biometrics at Receptos Inc. from 2014 to 2016, where he built the biostatistics and data management functions while contributing to mid- and late-stage development programs for ozanimod (Zeposia) in multiple sclerosis (MS) and inflammatory bowel diseases (IBD). Before joining Receptos, Mr. Cravets was the head of biostatistics at Ardea Biosciences from 2011-2014, building the biostatistics function while also making significant contributions to the designs and analyses of late-stage studies of lesinurad (Zurampic) for the treatment of gout. From 2003-2011 Mr. Cravets served in roles of increasing responsibility in the biostatistics group at Biogen Idec Inc., contributing to the successful regulatory approvals of rituximab (Rituxan) in both rheumatoid arthritis (RA) and chronic lymphocytic leukemia (CLL). From 1996 to 2003, Mr. Cravets was in the biostatistics group at Amgen, Inc., working on multiple products across various neurology, rheumatology, cardiovascular, and bone disease indications. Mr. Cravets began his career in the pharmaceutical products division of Abbott Laboratories in 1994 after completing his master’s degree in statistics at the University of Michigan and his bachelor’s degree in mathematics at UCLA.

Latha Satish, M.Sc., M.Phil, Ph.D.

Dr. Satish is a trained biotechnologist with several years of experience in cell and molecular biology. Dr. Satish’s interest has been in skin research with a special focus on skin inflammation, infection, and fibrosis. The other arm of Dr. Satish’s research has been to study the molecular determinants of palmar fascial disease, Dupuytren’s contracture.

Her long-term interest has been to develop therapeutic agents to help alleviate the pain and distress of patients with Dupuytren’s. Her studies on Dupuytren’s disease were funded by a private donor, which moved the research forward to study this disease in an animal model, which was not feasible earlier. Dr. Satish’s research on Dupuytren has identified small molecules that can be used as a target to intervene with the progression and development of the disease.

Dr. Satish received her Ph.D. from a prestigious institute in India and did her post-doctoral training at the University of Pittsburgh. Currently, Dr. Satish serves as a faculty at the Division of Asthma Research, Cincinnati Children’s Hospital; named as the top hospital in the US. At Cincinnati Children’s, Dr. Satish researches Atopic Dermatitis, a chronic inflammatory skin disease affecting children and adults. Dr. Satish has published over 50 articles in peer-reviewed journals, review articles and book chapters.

Dr. Keith Denkler

Dr. Denkler is an accomplished, board certified plastic surgeon with expertise in aesthetic and reconstructive surgery. Dr. Denkler is a clinical professor of plastic surgery at UCSF and has a private practice in Marin County.

He is internationally renowned for his use of multiple approaches in treating the debilitating and disabling effects of palmar fibromatosis (Dupuytren disease). Dr. Denkler is an expert in needle aponeurotomy (NA), a minimally invasive procedure that uses subcutaneous needles to release the contracture as well as use of subcutaneous injection of collagenase. He has treated over 10,000 Dupuytren’s fingers, authored >35 publications and book chapters, presented internationally and domestically and is often cited for expert opinion in national and international news discussing Dupuytren’s. HIs pioneering investigational work documenting the safety of epinephrine with local anesthesia contributed to the origination of “wide-awake hand surgery”.

Dr. Denkler trained at prestigious medical institutions in the United States and Europe. He attended Baylor College of Medicine in Houston, Texas, followed by residency training in plastic and reconstructive surgery with the Cronin, Bauer, and Biggs group, also in Houston. Additionally, Dr. Denkler completed a hand surgery fellowship with Dr. Eugene Kilgore in San Francisco and one year of fellowship training in craniofacial surgery with Dr. Paul Tessier in Paris, France.

Dr. daiva bajorunas

Daiva Bajorunas MD is an endocrinologist with more than 25 years of experience in the biopharmaceutical industry.  She has a strong interest in advancing therapeutic options for conditions of significant unmet medical need. 

For the past decade, Daiva has been engaged as a consultant to the pharmaceutical industry, currently as Founder and Principal, DBMD Consulting, and previously as Chief Medical Officer / Chief Scientific Officer for Vault Bioventures. She has provided her expertise to enhance large, mid-size and small pharmaceutical company product development, clinical/regulatory, and life cycle strategies for both drugs and devices, including oral, transdermal, injectable and inhalative delivery systems, working across multiple therapeutic areas and geographies. She has considerable experience chairing Data Safety Monitoring Boards.   

In the past she held various R&D positions of increasing responsibility at Rhone-Poulenc Rorer, BMS, Aventis (acquired by Sanofi), and Kos Pharmaceuticals (acquired by Abbott). Before she joined industry, she held academic appointments at Memorial Sloan-Kettering Cancer Center and Cornell University Medical College (CUMC), and was Director of Clinical Care, Endocrinology Service, Memorial Hospital (MH), New York, NY. Daiva received her MD degree at the University of Michigan Medical School, did her residency training at St. Vincent’s Hospital & Medical Center in NY, her metabolism fellowship at Stanford University Medical Center, CA and her endocrinology fellowship at MH/CUMC, NY.