ProcessMAP partners with Hg

HG Capital

ProcessMap partners with Hg, a global software investor, to accelerate its strategy towards becoming a global software leader in worker health and safety management

Hg’s strategic investment will accelerate ProcessMAP’s position towards a category leader in the rapidly growing EHS Risk and Compliance software sector.

Ft. Lauderdale, Florida, USA and New York, New York, USA.  5 January 2022.

ProcessMAP Corporation (“ProcessMAP”), a leading Environmental, Health and Safety (“EHS”) software platform provider, announced today that Hg, a leading software and services investor with nearly $40 billion funds under management, has agreed to make a significant investment in the business to accelerate ProcessMAP’s growth and expansion, and help solidify the company’s position as a global leader in the EHS software sector.

Following the transaction, ProcessMAP’s management team will retain a significant stake in the business. The terms of the transaction are not disclosed.

Founded in 2000, ProcessMAP’s vision is to enable businesses to proactively mitigate workplace health and safety risks for workers. ProcessMAP’s SaaS and mobile solutions serve mid-market and enterprise customers across large industry verticals such as automotive and manufacturing. ProcessMAP’s solutions are used by global customers in more than 140 countries, covering 2 million workers across 80,000 sites. Headquartered in Florida, ProcessMAP has nearly 300 employees based in the USA, Canada, the UK, Germany and India. The company is regularly recognized as a “Leader” in the biennial Green Quadrant report for EHS software published by Verdantix, an independent industry analyst for the EHS sector.

Accelerating the Innovation Momentum for ProcessMAP Customers

ProcessMAP will leverage the financial investment as well as Hg’s 20+ years of industry-leading experience in building and rapidly growing innovative software businesses.  The financial partnership with Hg will also enable ProcessMAP to deliver next-generation, smart and connected EHS solutions to its customers globally. Additionally, the company will also make investments to expand its team globally, strengthen its position further, and broaden its global customer base, particularly in Europe and Asia-Pacific.

Comments on the News

“We share our customers’ commitment to create and offer the safest and the healthiest workplaces, while minimizing the environmental impact of day-to-day operations. Bringing in Hg to invest in our business comes at a very interesting time as we see an opportunity to help customers protect millions more workers globally.”

Dave Rath, CEO and Co-Founder of ProcessMAP

“This partnership, built on software knowledge and experience, will enable us to develop our analytics-driven software further, helping more customers across the globe optimize their EHS processes while, critically, mitigating operational and sustainability risk.”

Jagan Garimella, CTO and Co-Founder of ProcessMAP

“Hg has been focused on risk and compliance software for two decades and we see strong tailwinds continuing to drive demand in this sector. The impressive work from Dave Rath, Jagan Garimella, and the team means that ProcessMAP is well-positioned to benefit from this dynamic. They’ve built a high-quality platform which receives consistent, strong feedback from a loyal customer base. We believe that together, Hg and ProcessMAP, will form a strong partnership and we look forward to supporting the team, investing in the business and continuing to realize its growth potential.”

Ben Meyer, Partner at Hg

KPMG Corporate Finance acted as the exclusive investment banking advisor to ProcessMAP.


Media Contacts

Hg
Tom Eckersley
Tom.Eckersley@hgcapital.com
+44 208 148 5401

Alex Yankus and Harry Mayfield (Brunswick, USA)
+1 917 818 5204

ProcessMAP
Sandeep Rath
Director, Global Product Marketing and Analyst Relations
srath@processmap.com

About ProcessMAP Corporation

ProcessMAP Corporation is the most trusted name for a digitization and process transformation platform that empowers customers to ensure workers’ health & safety, minimize risk, and assure compliance. The ProcessMAP Platform includes solutions for Environmental, Health and Safety (EHS), Environmental, Social and Governance (ESG), and Operational Risk Management (ORM), Industrial IoT, and actionable data analytics to connect people, systems, assets, and facilities to drive a Sustainable Enterprise. ProcessMAP is headquartered in Ft. Lauderdale, Florida, with locations across the globe, serving customers in over 140 countries. Visit https://www.processmap.com/ to learn more.

About Hg

Hg is a growth platform for software and services champions, focused on backing businesses that change how we all do business. Deep technology expertise, complemented by vertical application specialisation and dedicated operational support, provides a compelling proposition to management teams looking to scale their businesses. Hg has funds under management of around $40 billion, with an investment team of over 140 professionals, plus a portfolio team of around 40 operators, providing practical support to help our businesses to realise their growth ambitions. Based in London, Munich and New York, Hg has a portfolio of over 35 software and technology businesses, worth around $92 billion aggregate enterprise value, with over 55,000 employees globally, growing at over 20% per year. Visit www.hgcapital.com for more information.

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RTI Surgical announces spin-off of businesses into two independent companies

Montagu

Metals business will become Resolve Surgical Technologies
Tissues & Biologics business will retain the RTI Surgical name

 

RTI Surgical, a global private label OEM company, announced today that the company will spin off its Metals business, creating two independent companies that are focused on the needs of customers and patients in their distinct market segments. Ownership of both companies will be retained by Montagu, a leading private equity firm specialized in finding and growing businesses that make the world work.

As industry-leading surgical implant suppliers, both businesses partner with leading medical technology companies to design and develop medical devices. The spin-off will reinforce market focus for both the Metals and Tissue & Biologics businesses and better position each company to capitalize on strategic growth opportunities as the need for outsourced private label medical device manufacturing and product life cycle management increases.

 

Metals Business Introduces New Market Brand

As a result of the spin-off, the Metals business, which acts as a full-service partner covering design, development, manufacturing, and regulatory support of metal and polymer implants and instruments used in orthopedics, spine and cardiothoracic applications, will change its name and market brand to Resolve Surgical Technologies. The new name reflects the company’s commitment to resolve customers’ end-to-end manufacturing and product lifecycle challenges, so they are free to focus on their strategic priorities.

The current President of the Metals business, Megan Osorio, will become CEO of Resolve Surgical Technologies, focusing on meeting the growing demand for fully outsourced solutions, “Since the company was founded 30 years ago, our hallmark has been innovative product development, world-class manufacturing, rigorous quality management, and regulatory expertise. Our new brand carries this equity forward and communicates our exciting direction as an independent company,” said Osorio.

Since the company was founded 30 years ago, our hallmark has been innovative product development, world-class manufacturing, rigorous quality management, and regulatory expertise.

Megan Osorio, CEO, Resolve Surgical Technologies

Resolve Surgical Technologies was founded in Marquette, Mich. in 1992 as Pioneer Surgical Technologies and was acquired by RTI Surgical in 2013. The company will build on its Marquette facility and workforce.

 

Tissues & Biologics Business to Retain RTI Surgical Name

The Tissues & Biologics business, which provides a comprehensive portfolio of tissue-based surgical implants across multiple market segments and commercial channels, will retain the RTI Surgical name. Olivier Visa, CEO, will continue to lead this company, which is based in Alachua, Fla., and has manufacturing facilities in Greenville, N.C. and Neunkirchen, Germany. “Our team is passionate about partnering with our customers to develop and deliver solutions that restore quality of life for patients while maximizing the gift of tissue donation. With RTI Surgical’s singular focus on allograft and xenograft tissue-based implants, our team will provide expanded private label solutions for customers. Our expertise includes design, development, and processing in addition to all aspects of product life cycle management, regulatory compliance and Design History File ownership,” said Visa.

Our team is passionate about partnering with our customers to develop and deliver solutions that restore quality of life for patients while maximizing the gift of tissue donation.

Olivier Visa, CEO, RTI Surgical

RTI was the first company to offer precision-tooled bone implants and assembled technology to maximize each gift of tissue donation. The company was also the first to introduce proprietary, validated, tissue-specific sterilization processes that address the risk of donor-to-recipient disease transmission.

“This is an exciting opportunity for both businesses to pursue their growth potential as strong, independent companies,” said Adrien Sassi, Director at Montagu. “This milestone builds on our expertise in carve-outs and commitment to helping our businesses reach their full potential. We are fully committed to supporting Olivier, Megan and their teams as they build on their respective track records of innovation.”

This is an exciting opportunity for both businesses to pursue their growth potential as strong, independent companies.

Adrien Sassi, Director, Montagu

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EQT Private Equity and Santo to invest further in WS Audiology

eqt

EQT VIII and Santo Holdings to acquire EQT VI and its co-investors’ stakes in WS Audiology, the number one global pure play producer of hearing aids

WS Audiology is supported by strong, underlying macro trends, such as a growing aging population, urban noise pollution, and increased penetration and growing demand for hearing aids in developing countries

The investment by EQT Private Equity illustrates the long-term commitment and support for WS Audiology’s mission of helping people regain or improve their hear

EQT is pleased to announce that the EQT VIII fund (“EQT VIII” or “EQT Private Equity”) and Santo Holdings (“Santo”), together with co-investors,have agreed to acquire the EQT VI fundand its co-investors’ stakes in WS Audiology (“the Company”). Following the closing of the transaction, EQT VII, EQT VIII, Santo Holdings, the Tøpholm and Westermann families, and a group of minority co-investors, will own WS Audiology.

Headquartered in Lynge, Denmark, WS Audiology is the number one global pure play producer of hearing aids and accessories in terms of volumes with more than 170 years of combined experience and a proven track record as an industry innovator.

WS Audiology was created in February 2019 through the merger of Sivantos, acquired by EQT VI in 2014 and previously named Siemens Audiology Solutions, and Widex, at the time owned by the Tøpholm and Westermann families. As part of the merger EQT VII and EQT VIII jointly invested in the combined company alongside EQT VI, Santo, the Tøpholm and Westermann families, and other minority shareholders. Today, WS Audiology has revenues of more than EUR 2.0 billion, over 11,000 employees and one of the strongest R&D teams in the industry.

WS Audiology operates in a highly attractive market characterized by healthy, non-cyclical growth and broadened addressable customer groups. The Company is supported by underlying trends, such as an overall aging population, urban noise pollution resulting in higher numbers of hearing-impaired people, an increasing penetration of hearing aids users among the hearing impaired thanks to improved technology and social acceptance, and a growing demand for hearing aids in developing countries.

Since acquisition, WS Audiology’s EBITDA has increased more than 20 percent. EQT and the owner families have supported the Company’s efforts to invest significantly in R&D to entrench as the industry innovator, benefitting from a unique digital ecosystem. WS Audiology is the leader in remote fitting of hearing aid equipment through its subsidiary hear.com, and COVID-19 has accelerated tele-audiology and remote fitting trends.

Kasper Knokgaard, Partner within EQT Private Equity Advisory Team, “Every year, WS Audiology helps millions of people around the world to regain or improve their hearing. The Company’s hearing aids not only improve quality of life but they also offer the possibility to change people’s economic opportunities to the better in less developed countries. EQT Private Equity is therefore proud to renew its long-term support for WS Audiology alongside its other co-investors.

The transaction is subject to customary conditions and approvals and it closed in December 2021.

With this transaction, EQT VIII is expected to be 80-85 percent invested (including closed and/or signed investments, announced public offers, if applicable, and less any expected syndication).

Contact
EQT Press Office, press@eqtpartners.com, +46 8 506 55 334

About

About EQT
EQT is a purpose-driven global investment organization with more than EUR 70 billion in assets under management across 27 active funds. EQT funds have portfolio companies in Europe, Asia-Pacific and the Americas with total sales of approximately EUR 29 billion and more than 175,000 employees. EQT works with portfolio companies to achieve sustainable growth, operational excellence and market leadership.

More info: www.eqtgroup.com
Follow EQT on LinkedInTwitterYouTube and Instagram

About WS Audiology
Formed in 2019, through the merger of Sivantos and Widex, WS Audiology combines over 140 years’ experience in pioneering the use of technology to help people with hearing loss hear the sounds that make life wonderful. With truly differentiated brands like Widex, Signia, Rexton, Audio Service and Vibe, and with diverse assets across wholesale, retail, online, managed care and diagnostic solutions, we are active in over 125 markets. As a global leader, our ambition is to unlock human potential by making wonderful sound part of everyone’s life.

More info: www.wsa.com

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Gilde Healthcare portfolio Volta Medical treats first U.S. patients with persistent cardiac arrythmias

GIlde Healthcare
December 21, 2021
Marseille, France, Providence (Rhode Island), USA & Utrecht, the Netherlands

Volta Medical, a pioneering health tech company developing artificial intelligence (AI)-based software solutions to treat cardiac arrythmias, today announced the introduction of its leading-edge product, VX1, at three leading U.S. hospitals. New York Presbyterian Queens, Northwell Health’s Lenox Hill Hospital in New York City, and Ascension St. Vincent’s Riverside, Jacksonville, FL, are the first U.S. hospitals to implement VX1, which is designed to improve outcomes for patients undergoing atrial fibrillation (AF) ablation procedures.

 

All three hospitals also are recruiting AF ablation patients to participate in an international, randomized controlled clinical trial to evaluate the outcomes of VX1-guided ablation versus standard ablation called TAILORED-AF trial. The international, multi-center trial will involve 25 sites and 342 patients and is expected to report results in 2024. VX1 is cleared as a medical device by the U.S. Food and Drug Administration and CE-certified by the European Union.

VX1 is the first commercially available AI software to help clinicians combat high failure rates in the use of ablation for treating persistent, drug-resistant AF. AF, characterized by an irregular and chaotic heartbeat (cardiac arrythmia), can lead to more serious health issues such as heart failure and stroke. During AF ablation, a specialized cardiologist known as an electrophysiologist inserts catheters through the blood vessels into the heart to burn or freeze tissue that is causing abnormal electrical signals in the upper chamber, or atrium. The procedure creates scarring that restores a normal heartbeat.

The VX1 system analyzes electrical signals measured during the procedure and identifies abnormalities in real-time. VX1 is versatile and can be installed in most operating rooms and is compatible with the main multipolar catheters and mapping systems.

About atrial fibrillation (AFib or AF)
An estimated 6.1 million people in the United States have AF with projections to reach nearly 12.1 million in 2030. Worldwide, it affects more than 33 million people. Symptoms include palpitations, lightheadedness and shortness of breath. In some patients, AF can lead to heart failure. AF is not only an extremely costly public health issue but also a major risk factor for stroke, posing a 4-to-5 times greater risk than for the general population. AF is commonly treated with medication that regulates or slows the heart rate. For patients who cannot tolerate or are resistant to anti-arrhythmic drug therapy, ablation is the current standard of care. Ablation uses heat or cold energy to create tiny scars in the heart to block abnormal electrical signals and restore a normal heartbeat. However, the efficacy of this approach depends largely on the experience and intuition of the electrophysiologist. With 50% of persistent AF patients requiring repeat treatments, the need for more precise therapies is significant.

About the TAILORED-AF trial
TAILORED-AF is an international, multicenter trial designed to determine if a tailored VX1 AI software-guided ablation strategy targeting areas of spatiotemporal dispersion in combination with pulmonary vein isolation (PVI) is superior to a conventional anatomical ablation strategy targeting PVI alone for the treatment of persistent AF. The primary endpoint of the study is the absence of documented AF episodes > 30 seconds, with or without anti-arrhythmic drugs (AADs), 12 months after a single index ablation procedure. Secondary endpoints include absence of AF and/or atrial tachycardia (AT) episodes after a 12-month period, following one or more procedures, as well as safety. Volta Medical expects results from the TAILORED-AF trial in 2024.

About Volta Medical
Volta Medical is a health tech company developing AI software solutions to assist cardiac electrophysiologists in the operating room. Volta’s overarching goal is to significantly improve cardiac arrythmia management by developing state-of-the-art, data-driven medical devices based on large databases of procedural data with the highest standards of data protection. Founded by three physicians and a data scientist in 2016 in Marseille, France, Volta’s first product, VX1, assists cardiologists in the real-time identification of specific abnormal electrograms, known as dispersed electrograms. For more information, visit the company’s website at www.volta-medical.com.

About Gilde Healthcare
Gilde Healthcare is a specialized healthcare investor with two fund strategies: Venture&Growth and Private Equity. The firm operates out of offices in Utrecht (The Netherlands), Frankfurt (Germany) and Cambridge (United States). Gilde Healthcare Venture&Growth invests in fast growing, innovative companies active in (bio)pharmaceuticals, healthtech and medtech that are based in Europe and North America. For more information, please visit: www.gildehealthcare.com.

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Ardian sells SCHWIND eye-tech-solutions, a leading provider of eye laser systems, to Adagia Partners

Ardian

Frankfurt am Main/Kleinostheim, December 21, 2021 – Ardian, a world-leading private investment house, has reached an agreement to sell its majority stake in SCHWIND eye-tech-solutions GmbH (“SCHWIND”) – one of the world’s leading specialists in laser systems for the treatment of vision defects and corneal diseases – to the private equity company Adagia Partners.

Through its partnership with Ardian, SCHWIND’s management team, led by CEO Rolf Schwind, was strengthened with the appointment of COO Domenic von Planta and CFO Dirk Rosenlöcher and will continue to manage the business in the future. The parties have agreed not to disclose details of the transaction.

Founded in 1958, the company develops, produces and distributes an extensive and highly sophisticated range of products. These include diagnostic tools and state-of-the-art laser systems for the treatment of vision defects and corneal diseases, as well as corresponding software solutions and services.

Worldwide, more than 1,300 SCHWIND laser systems are currently installed in ophthalmology practices, eye clinics, laser centers and university hospitals in over 100 countries. SCHWIND laser systems are used in LASIK, LASEK, PRK, TransPRK and Femto-LASIK eye surgery as well as in minimally invasive lenticle extraction. The combination of innovative technology and intelligent device design ensures maximum precision and safety in refractive corneal surgery. SCHWIND offers clients a one-step solution for the entire course of treatment, through an approach that encompasses the digital networking of diagnostic tools and eye laser system, as well as other supplementary services.

“SCHWIND is recognized as the most technologically advanced company in the sector. With Ardian as our partner, we have been able to successfully expand our unique specialization in the market. Investment in research and development to create the world’s most innovative and precise laser systems for refractive corneal has helped substantially strengthen our product portfolio and tap into new application areas. Our products in the growing market for ophthalmology stand for the highest quality and absolute reliability. We would like to thank the Ardian team as well as the new partner Adagia Partners for their excellent cooperation over the past five years.” Rolf Schwind, CEO of SCHWIND eye-tech-solutions GmbH

“SCHWIND enjoys a worldwide reputation for cutting-edge technology in eye surgery. We are proud to have made a contribution to the successful development of the company in recent years and to have played a part in laying the foundation for a successful future with the addition of the ATOS Femtosecond laser to the product portfolio. We would like to thank the management team led by CEO Rolf Schwind and COO Domenic von Planta for the cooperation. Together with the extended leadership team and the employees of SCHWIND, management have steadily and systematically developed the company with innovative technology solutions and strengthened their global leadership position in refractive corneal surgery. We wish the company and its employees all the best for the future.” Dirk Wittneben, Managing Director & Head of Expansion Germany at Ardian

With Ardian as a partner, the company has invested significantly in research and development since 2016, and Ardian has supported the company with experienced sector experts. As a result, the product range, which previously consisted of various excimer lasers and diagnostic devices, could be expanded with a specially developed intelligent femtosecond laser system (ATOS). Femtosecond lasers enable state-of-the-art surgical methods on the eye to improve vision, such as minimally invasive lenticle extraction or flap creation as part of FemtoLASIK. For each operation with a femtosecond laser, high-quality consumables developed by SCHWIND (patient interfaces) are used, which physically connect the laser device to the patient’s eye. As a result, SCHWIND was able to expand its core business of developing and marketing eye laser and diagnostic systems with additional recurring revenues through patient interfaces for ATOS femtosecond laser treatments. In addition to the successful core business with excimer laser systems and diagnostic devices, the entry into the market segment of femtosecond lasers represents a key step in continuing the strong organic growth and the successful corporate development of SCHWIND.

ABOUT ARDIAN

Ardian is a world-leading private investment house with assets of US$120bn managed or advised in Europe, the Americas and Asia. The company is majority-owned by its employees. It keeps entrepreneurship at its heart and focuses on delivering excellent investment performance to its global investor base.
Through its commitment to shared outcomes for all stakeholders, Ardian’s activities fuel individual, corporate and economic growth around the world.
Holding close its core values of excellence, loyalty and entrepreneurship, Ardian maintains a truly global network, with more than 800 employees working from fifteen offices across Europe (Frankfurt, Jersey, London, Luxembourg, Madrid, Milan, Paris and Zurich), the Americas (New York, San Francisco and Santiago) and Asia (Beijing, Singapore, Tokyo and Seoul). It manages funds on behalf of more than 1,200 clients through five pillars of investment expertise: Fund of Funds, Direct Funds, Infrastructure, Real Estate and Private Debt.

www.ardian.com

ABOUT SCHWIND

SCHWIND eye-tech-solutions is one of the technological leaders in the global market for refractive and therapeutic corneal surgery. The family business develops, produces and markets a comprehensive, highly developed product portfolio for the treatment of vision defects and corneal diseases. With the SCHWIND AMARIS Excimer Laser product family and the SCHWIND ATOS femtosecond laser, the company covers the most important all-laser procedures of modern refractive surgery from a single source: the touch free TransPRK/SmartSurfACE surface treatment, intrastromal FemtoLASIK and minimally invasive SCHWIND SmartSight lenticle extraction of the new generation. Eye surgeons in more than 100 countries treat their patients with SCHWIND technologies.

www.eye-tech-solutions.com

ABOUT ADAGIA PARTNERS

Adagia Partners is a pan-European mid-market private equity firm with offices in Frankfurt and Paris. The firm was created and is owned by its Partners. The team is made of 15 professionals with international and operational background. The firm is delivering performance for all stakeholders by fostering entrepreneurship and humanism.
Adagia Capital Europe, the €750m investment vehicle currently in fund raising, will be deployed in Midcap companies in France, Germany, Benelux, Switzerland and Austria. The fund has an industry specialist approach and focusses on Healthcare, Business Services and Tech Industries.
The fund backs entrepreneurs in the implementation of their growth strategies, build-up and Tech-Digital approach.

List of participants

  • Ardian Team: Dirk Wittneben, Yannic Metzger, Marlon Sandvoss
    • M&A Advisory: Macquarie Capital (Florian Geiger, Dr. Fabian Trübenbach)
    • Commercial: L.E.K. Consulting (Tobias Koesters)
    • Legal: White & Case (Dr. Stefan Koch, Tomislav Vrabec)
    • Financial: PwC (Peter Gröninger)
    • Tax: Taxess (Gerald Thomas, Richard Schäfer)

MEDIA CONTACTS

ARDIAN

CHARLES BARKER

ardian@charlesbarker.de

Peter Steiner

+49 69 79409027

Tobias Eberle

+49 69 79409024

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Stella Kotipalvelut Ltd acquired by Finnish health services provider 9Lives

Tesi

Finnish 9Lives, specialised in demanding mobile health services, acquires Stella Kotipalvelut Ltd. The personnel of Stella, the company having seen strong growth in recent years, continues to work under 9Lives. By 2025, 9Lives aims to become the Northern-European leading provider of mobile, local social and healthcare services.

The fusion will be finalised during 2022. Stella is owned by Intera Fund II Ky, Tesi (Finnish Industry Investment Ltd), Posti Group Ltd as well as the management. Tesi made the initial investment in the company in 2014, to support the good conditions for growth and social impact the company had in social and healthcare services sector.

Read more:

Press release by Stella Kotipalvelut Ltd 20.12.2021 (in Finnish)

More information:

Miikka Salminen, Investment Manager, Tesi
miikka.salminen@tesi.fi
+358 40 535 4758

 

Tesi (Finnish Industry Investment Ltd) is a state-owned investment company that wants to raise Finland to the front ranks of transformative economic growth by investing in funds and directly in companies. We invest profitably and responsibly, hand-in-hand with private co-investors, to create new success stories. Our investments under management total 2.1 billion euros. www.tesi.fi | @TesiFII

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Vera Therapeutics Announces Acquisition of Monoclonal Antibody From Pfizer to Treat BK Virus in Transplant Patients

Abingworth

Ongoing Phase 2 clinical trial for MAU868 in kidney transplant patients; potential first-in-class

MAU868 Phase 2 data for kidney transplant to readout mid-2022

BK Virus is a leading cause of transplant loss and transplant-associated morbidity

BRISBANE, Calif., Dec. 17, 2021 (GLOBE NEWSWIRE) — Vera Therapeutics, Inc. (Nasdaq: VERA), a clinical-stage biotechnology company focused on developing treatments for immunological diseases that improve patients’ lives, announced today that it has acquired MAU868, a first-in-class monoclonal antibody to treat BK Virus (BKV) infections, and has entered into a credit facility with Oxford Finance LLC (Oxford) to provide borrowing capacity up to $50 million. MAU868, acquired from Amplyx Pharmaceuticals, Inc., a wholly owned subsidiary of Pfizer Inc., has the potential to neutralize infection by blocking BKV virions from binding to host cells.

“BKV is a leading cause of kidney transplant loss and transplant-associated morbidity, and there are currently no available antiviral treatments in the U.S. We are excited to acquire MAU868 from Pfizer and carry it forward in development,” said Vera founder and CEO Marshall Fordyce, MD. “The acquisition of MAU868, a potentially transformative treatment for BKV, is consistent with our strategy to diversify our pipeline with new molecules that leverage our strengths and serve adjacent populations. We believe, based on currently available data, that MAU868 has the potential to significantly impact outcomes for kidney transplant patients and become the first effective therapy for BKV. We look forward to working with regulators to establish a new standard of care for kidney transplant patients.”

MAU868 is currently undergoing a randomized, double-blind, placebo-controlled Phase 2 clinical trial to assess the safety, pharmacokinetics, and efficacy for the treatment of BKV in kidney transplant patients. MAU868 has been shown in an interim analysis of week 12 data from Cohort 1 and 2 of a Phase 2 study to be well tolerated and showed a greater proportion of subjects with decrease in BK plasma viral load versus placebo. Full Cohort 1 and 2 interim analysis results will be submitted for presentation at a conference in mid-2022.

Up to 90 percent of healthy adults are infected with BKV, but it remains latent in kidney and bladder tissues. Reactivation occurs in the setting of immune suppression, and causes clinical disease in the transplant setting. BKV is a significant cause of complications in these immunocompromised patients, including in kidney transplant and hematopoietic stem cell transplant (HSCT) recipients. In kidney transplant recipients, BKV is a leading cause of allograft loss and poor outcomes, while in HSCT recipients, the virus significantly increases the risk of severe hemorrhagic cystitis, which causes bladder damage. There are currently no approved treatments for BKV in the U.S.

MAU868 Asset Acquisition
In partial consideration for the asset acquisition, Vera made an upfront payment of $5.0 million. In addition to the upfront payment, Vera is also obligated to make certain milestone payments in an aggregate amount of up to $7.0 million based on certain regulatory milestones. Further, Vera is required to pay Amplyx low single-digit percentage royalties based on net sales on a country-by-country and product-by-product basis. The rights to MAU868 that Vera acquired from Amplyx are subject to a license agreement by and between Amplyx and Novartis International Pharmaceutical AG, pursuant to which Vera is obligated to make certain milestone payments in an aggregate amount of up to $69.0 million based on certain clinical development, regulatory and sales milestones. Further, the Company is required to pay Novartis mid-to-high single-digit percentage royalties based on net sales on a country-by-country and product-by-product basis.

Credit Facility
Vera also announced today that they entered into a credit facility with Oxford Finance. Under the terms of the loan agreement, Oxford will provide Vera with borrowing capacity of up to $50 million. The initial $5 million funded at closing, and an additional $45 million will be available in minimum draws of $5 million, at Vera’s option through the end of 2022. The debt facility provides for at least 48-months of interest-only at close. There are no warrants or financial covenants associated with the credit facility. Armentum Partners served as the Company’s financial advisor on the debt financing.

About Vera
Vera Therapeutics is a clinical-stage biotechnology company focused on developing treatments for serious immunological diseases. Vera’s mission is to advance treatments that target the source of immunologic diseases in order to change the standard of care for patients. Vera’s lead product candidate is atacicept, a fusion protein self-administered as a subcutaneous injection once weekly that blocks both B lymphocyte stimulator (BLyS) and a proliferation-inducing ligand (APRIL), which stimulate B cells and plasma cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN), also known as Berger’s disease. Vera is also developing MAU868, a monoclonal antibody that neutralizes infection with BK Virus, a polyomavirus that can have devastating consequences in certain settings such as kidney transplant. For more information, please visit www.veratx.com.

Forward-looking Statements

Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements include statements regarding, among other things, the potential efficacy of our product candidates, research and clinical development plans, the scope, progress, and results of developing our product candidates, strategy, regulatory matters, including the timing and likelihood of success of obtaining drug approvals, market opportunity and our ability to complete certain milestones, the timing of the expected closing of the debt financing, and the expected use of the net proceeds therefrom. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Words such as “plans,” “will,” “anticipates,” “goal,” “potential,” and similar expressions are intended to identify forward-looking statements. These forward-looking statements are based upon Vera’s current expectations and involve assumptions that may never materialize or may prove to be incorrect. Actual results could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, which include, without limitation, risks related to the ability to realize the anticipated benefits of the acquisition, including the possibility that the expected benefits from the acquisition will not be realized or will not be realized within the expected time period, risks and uncertainties associated with Vera’s business in general, the impact of the COVID-19 pandemic, and the other risks described in Vera’s filings with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. Vera undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.

Contacts
Investor Contact:
IR@veratx.com

Media Contact:
Greig Communications, Inc.
Kathy Vincent
kathy@greigcommunications.com

 

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Milestone for Calliditas as FDA grants accelerated approval of TARPEYO™

December 16, 2021

Our portfolio company Calliditas Therapeutics reached a major milstone yesterday with its accelerated FDA approval of Tarpeyo™, a novel therapy indicated for patients with nephropathy. Industrifonden was the first institutional venture investor in Calliditas backing its mission to bring novel therapies to patients with high unmet needs in renal disease. This landmark achievement will bring a novel therapy in Tarpeyo™ to market in the US for a severe patient population with deterioration of kidney function, so called IgA nephrophaty. Calliditas Therapeutics listed successfully on NASDAQ Stockholm in 2018 and underwent a dual-listing on NASDAQ US in June 2020. We congratulate the entire Calliditas team lead by René Lucander and are glad to support our mission to back lifesciences companies bringing novel therapies to patients with severe health conditions and high unmet need for new therapies.

The press release from Calliditas Therapeutics can be read here.

/Patrik Sobocki, Investment Director, on behalf of the entire team at Industrifonden

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Philips acquires Gilde portfolio company Vesper Medical to further expand its image-guided therapy devices portfolio

GIlde Healthcare
December 14, 2021
Amsterdam & Utrecht (the Netherlands)

Royal Philips (NYSE: PHG; AEX: PHIA), a global leader in health technology, today announced that it has signed an agreement to acquire Vesper Medical Inc., a US-based medical technology company that develops minimally-invasive peripheral vascular devices. Vesper Medical, a portfolio company of Gilde Healthcare, will further expand Philips’ portfolio of diagnostic and therapeutic devices with an advanced venous stent portfolio for the treatment of deep venous disease. The transaction, which is subject to customary closing conditions, is expected to be completed in the first quarter of 2022. Financial details of the transaction were not disclosed.

Complementing Philips’ strong intravascular ultrasound (IVUS) offering in venous imaging, Vesper Medical will add a venous stenting solution to address the root cause of chronic deep venous disease (DVD). The Vesper DUO Venous Stent System® consists of venous stents intended to treat deep venous obstruction. Uniquely engineered to address the multiple anatomical challenges of the deep venous system, it provides physicians with a modular portfolio to customize therapy, restore venous flow, and resolve the painful symptoms of deep venous disease for the broad range of patients suffering from chronic venous insufficiency.

The acquisition of Vesper Medical is another step in our objective to innovate patient treatment with more sophisticated technology and expand our growth in the vascular therapy space.

Chris Landon, Senior Vice President and General Manager Image Guided Therapy Devices at Philips:
“The acquisition of Vesper Medical is another step in our objective to innovate patient treatment with more sophisticated technology and expand our growth in the vascular therapy space,” said Chris Landon, Senior Vice President and General Manager Image Guided Therapy Devices at Philips. “Leveraging our significant procedural expertise, we see strong clinical synergies between Vesper Medical’s innovative stenting solution and our existing peripheral vascular offering. This combined offering will help to better support clinicians to decide, guide, treat and confirm during the procedure, thereby enhancing patient care.”

“I am proud that Philips will become the home for our innovations and our people, joining forces to shape the future of treating deep venous disease,” said Bruce Shook, President and CEO of Vesper Medical. “I look forward to further advance our next generation venous technology and bring it to patients and clinicians globally, together with Philips.”

Vesper Medical was founded in 2016 and is headquartered in Wayne, Pennsylvania, US. Upon completion of the transaction, Vesper Medical and approximately 20 of its employees will become part of Philips’ Image-Guided Therapy business.

About Gilde Healthcare
Gilde Healthcare is a specialized healthcare investor with two fund strategies: Venture&Growth and Private Equity. The firm operates out of offices in Utrecht (The Netherlands), Frankfurt (Germany) and Cambridge (United States). Gilde Healthcare Venture&Growth invests in fast growing, innovative companies active in (bio)pharmaceuticals, healthtech and medtech that are based in Europe and North America. For more information, please visit: www.gildehealthcare.com.

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EQT Private Equity to invest in 3Shape, a global leader in digital dentistry

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EQT Private Equity to acquire a minority stake in 3Shape, a global leading player and innovator in digital dentistry focused on intra-oral scanners, CAD and CAM software for dental clinics and the dental lab market

3Shape’s products are at the forefront of driving digitalization of dentist workflows, reducing material consumption and improving preventive care and patient outcomes

3Shape will leverage the expertise from EQT’s in-house digitalization team, global healthcare sector team, and global advisory network, in its next chapter of growth, focusing on continued international expansion and roll-out of additional digital services

EQT is pleased to announce that the EQT IX fund (“EQT Private Equity”) has agreed to acquire a 20 percent stake in 3Shape (the “Company”) from its founders, who will remain majority shareholders in the Company. Together with the founders and management, EQT Private Equity will support and accelerate execution of 3Shape’s strategic vision to continue to lead the digitalization of the global dental industry.

Based in Copenhagen, Denmark, 3Shape is a global leader in digital dentistry and provides state of the art intra-oral scanning solutions, CAD (Computer Aided Design) and CAM (Computer Aided Manufacturing) software for dentists and dental laboratories in over 100 countries. The Company was founded in 2000 and employs more than 1,900 people in Europe, Americas and Asia, of which approximately 500 sit in R&D.

3Shape operates in a highly attractive sub-segment of the Dental Equipment and Software market growing at around 15 percent per year, driven by the digitalization of dental workflows to provide improved and more efficient care. The market is supported by long-term secular growth drivers including an aging population, higher disposable income, and increasing demand for aesthetic treatments. 3Shape is uniquely positioned at the nexus of the digital workflow to drive the digital transformation, and thereby improving patient care and reducing the environmental footprint of analogue supply chains and processes.

EQT Private Equity will support 3Shape’s vision to further internationalize and drive significant global growth while continuing to innovate and deliver unique digital solutions globally. The Company will be able to leverage and benefit from the full EQT platform, including EQT’s in-house digital teams, its global healthcare sector team, the broad experience from EQT’s advisory network, as well as strong ESG capabilities, to support 3Shape’s continued growth journey.

Mads Ditlevsen, Partner within EQT Private Equity’s Advisory Team, commented, “Having followed 3Shape closely for more than a decade, we are highly impressed with its high pace of innovation and ability to drive the digitalization of the dental industry, cementing its position as a global market leader. We see significant global potential for 3Shape and EQT looks forward to contributing to its continued development in close collaboration with its founders, board and the management team.”

Michael Bauer, Partner and Co-Head of Healthcare within EQT Private Equity’s Advisor team, added, “We are very excited about the opportunity to partner with the 3Shape team and take an active role in its next growth phase. This investment is a testimony to EQT’s healthcare strategy and dedication to invest in global leading healthcare companies within attractive high-growth subsectors, which 3Shape is a perfect example of.”

Jørgen Jensen, Chairperson of 3Shape commented, “We are pleased with the confidence that EQT has shown us by investing a substantial amount in becoming a co-owner of the company. This long-term partnership will strengthen 3Shape and help us deliver on our vision of continued innovation, and thereby delivering unique digital solutions for the global dental industry. At the same time, this investment from such an esteemed investor confirms the strength of 3Shape’s business model and the company’s very exciting future.”

Jakob Just-Bomholt, CEO of 3Shape, added, “EQT will undoubtedly contribute knowledge and experience to support 3Shape’s continued growth journey. We have great ambitions, and we will continue to be the world leader in digitizing dental care. Our scanners are used by more than one million patient scans each month, and this number will increase significantly going forward. With our technology, dentists can effectively automate and digitize work flows, while offering diagnostic services that can prevent dental problems. We will do this, among other things, through our next-generation technology and our new 3Shape Unite platform. There is significant potential to deliver digital services and products to dentists around the world and 3Shape is in a unique position to capture the potential and continue to strengthen our position as the market leader.”

EQT Private Equity was advised by FIH Partners (M&A), Accura (Legal), EY (Financial & Tax), Ringstone (Technology), and The Footprint Firm (ESG). The transaction is expected to close during Q1 2022.

With this transaction, EQT IX is expected to be 75-80 percent invested (including closed and/or signed investments, announced public offers, if applicable, and less any expected syndication).

Contact
EQT Press Office, press@eqtpartners.com, +46 8 506 55 334

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