[April 16, 2018] |
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LimFlow Raises €27 Million ($33.5 Million) in Series C Financing Led by Sofinnova Partners to Advance Innovative Critical Limb Ischemia (CLI) Treatment
LimFlow
SA, developer of innovative, peripheral endovascular technology
transforming the treatment of critical limb ischemia (CLI), today
announced it has secured €27 million ($33.5 million) in an
oversubscribed Series C financing. The round was led by Sofinnova
Partners, with continued participation from existing round B investors
Bpifrance, the French sovereign investment bank, and Balestier, a
Singaporean family fund. Gérard Hascöet, Venture Partner at Sofinnova
Partners, and Dr. Kinam Hong, Partner of the Sofinnova Crossover I Fund,
will join the company's board of directors. The investment is the first
for the newly raised Sofinnova Crossover I Fund.
Proceeds from the Series C financing will fund the company's major
strategic initiatives through the second half of 2020, including
completion of a U.S. pivotal trial for the LimFlow Percutaneous Deep
Vein Arterialization System (pDVA), which will be submitted to the FDA
as part of the approval process, and execution of its international
commercialization strategy.
Based in Paris, LimFlow was founded in late 2012 by Dr. Martin Rothman,
a world-renowned interventional cardiologist, and MD Start, a European
Incubator dedicated to healthcare. The company's proprietary and CE
marked technology is a novel and purely percutaneous therapy for
"no-option" CLI patients when all other revascularization efforts have
been exhausted and a patient is facing a major amputation.
In the past 18 months, the company has achieved a number of key
milestones, including CE Mark and acceptance into the FDA Breakthrough
Dvices Program. Enrollment is also currently underway in both a U.S.
feasibility study of the LimFlow technology (PROMISE I) and an
international post-market study (PROMISE International).
"We are gratified with the support we have received from Sofinnova
Partners, a leading European venture capital firm and one of the most
respected and specialized global Life Sciences investors. We are equally
appreciative of the continued strong commitment from our existing
investors. The new funds will enable us to continue our mission to save
patients from amputation, and ultimately, save lives that might
otherwise be lost," said LimFlow CEO Dan Rose.
"LimFlow is an excellent fit for our healthcare Crossover I fund, where
we seek investments in companies with game-changing technologies that
address important clinical unmet needs and are led by experienced and
passionate management teams," said Dr. Hong.
About LimFlow SA
LimFlow
is a private, venture-backed medical device company transforming the
treatment of Critical Limb Ischemia, a growing clinical need in the face
of the prevalence of diabetes, heart disease and an aging population.
The LimFlow Percutaneous Deep Vein Arterialization (pDVA) System is
designed to bypass blocked arteries in the leg and rush oxygenated blood
back into the foot. For many patients, restoring perfusion in the lower
limbs resolves chronic pain, improves quality of life, promotes wound
healing and prevents major amputation. For more information, visit www.limflow.com.
About Sofinnova Partners
Sofinnova Partners is a leading European venture capital firm
specialized in Life Sciences. Based in Paris, France, the firm brings
together a team of professionals from all over Europe, the US and China.
The firm focuses on paradigm shifting technologies alongside visionary
entrepreneurs. Sofinnova Partners seeks to invest as a lead investor in
start-ups and corporate spin-offs and has backed nearly 500 companies
over more than 45 years, creating market leaders around the globe.
Today, Sofinnova Partners has over €1.9 billion under management For
more information, please visit: www.sofinnova.fr.
CAUTION: The LimFlow technology is approved for investigational use only
in the United States. The LimFlow System received the CE Mark in October
2016 and is currently available commercially in Europe. The LimFlow
System has not been approved for sale in the USA, Canada, or Japan.

View source version on businesswire.com: https://www.businesswire.com/news/home/20180416005163/en/
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