GlobeNewswire by notified

Aquablation Therapy is the first surgical robotics system to receive a MedTech Innovation Briefing (MIB) from the National Institute for Health Care Excellence

Share

REDWOOD CITY, Calif., March 07, 2023 (GLOBE NEWSWIRE) -- PROCEPT® BioRobotics Corporation today announced Aquablation Therapy received a MedTech Innovation Briefing (MIB) from the National Institute for Health Care Excellence (NICE), for benign prostate hyperplasia (BPH) in the United Kingdom. NICE has recognized Aquablation Therapy is as effective as transurethral resection of the prostate (TURP) for the removal of prostate tissue for men with BPH. A panel of clinical experts said the technology is innovative compared to the standard of care and offers additional benefits, such as increased ability to preserve sexual function. The clinical experts associated with the review stated that the technology has the potential to replace TURP and will challenge holmium laser enucleation for larger prostates.

Aquablation therapy is the first and only robotic surgical system to receive a MIB. MIBs are designed to support decision-making by health care professionals about the adoption and impact of new technology through detailed technical, clinical and economic assessments. New technology is selected on the basis of high demand on the topic, the potential for useful clinical outcomes, and whether evidence is available.

Mr. Neil Barber, one of the Briefings’ Clinical Experts and a PROCEPT BioRobotics consulting physician, stated, “We have been treating men successfully with Aquablation therapy for over seven years and believe it will soon become the standard of care for BPH. Patients ultimately want their work, leisure, and sex lives back without risking long-term catheterization or loss of sexual function. AquaBeam’s real time image guidance allows surgeons to see a patient’s anatomy through a multidimensional view, allowing for a fully customized treatment plan. The robot executes the treatment plan and guides the waterjet with speed and accuracy leading to a more consistent, predictable, and safer patient outcome. Moreover, it is much easier to train new urologists to become proficient using Aquablation therapy, which bodes well for the future.”

“The NICE MedTech Innovation Briefing further validates the value we believe Aquablation Therapy brings to patients, doctors, hospitals and healthcare systems around the world,” said Sham Shiblaq, Executive Vice President, Chief Commercial Officer of PROCEPT® BioRobotics. “The robust body of clinical evidence shows Aquablation therapy offers improved safety and durability when compared to transurethral resection of the prostate, which is the current gold standard surgical treatment option.”

About PROCEPT BioRobotics Corporation
PROCEPT BioRobotics is a surgical robotics company focused on advancing patient care by developing transformative solutions in urology. PROCEPT BioRobotics develops, manufactures and sells the AquaBeam Robotic System, an advanced, image-guided, surgical robotic system for use in minimally invasive urologic surgery with an initial focus on treating benign prostatic hyperplasia, or BPH. BPH is the most common prostate disease and impacts approximately 40 million men in the United States. PROCEPT BioRobotics designed Aquablation therapy to deliver effective, safe and durable outcomes for males suffering from lower urinary tract symptoms, or LUTS, due to BPH that are independent of prostate size and shape or surgeon experience. The Company has developed a significant and growing body of clinical evidence, which includes nine clinical studies and over 150 peer-reviewed publications, supporting the benefits and clinical advantages of Aquablation therapy.

Forward Looking Statements
This release contains forward‐looking statements within the meaning of federal securities laws, including with respect to the Company’s projected financial performance for full year 2022, statements regarding the potential utilities, values, benefits and advantages of Aquablation® therapy performed using PROCEPT BioRobotics’ products, including AquaBeam® Robotic System, which involve risks and uncertainties that could cause the actual results to differ materially from the anticipated results and expectations expressed in these forward-looking statements. You are cautioned not to place undue reliance on these forward-looking statements. Forward-looking statements are only predictions based on our current expectations, estimates, and assumptions, valid only as of the date they are made, and subject to risks and uncertainties, some of which we are not currently aware. Forward-looking statements may include statements regarding financial guidance, market opportunity and penetration, the Company’s possible or assumed future results of operations, including descriptions of the Company’s revenues, gross margin, profitability, operating expenses, installed base growth, commercial momentum, overall business or the overall macroeconomic environment, which may impact customer spending or the Company’s costs. Forward‐looking statements should not be read as a guarantee of future performance or results and may not necessarily be accurate indications of the times at, or by, which such performance or results will be achieved. These forward‐looking statements are based on the Company’s current expectations and inherently involve significant risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in such forward‐looking statements as a result of these risks and uncertainties. These risks and uncertainties are described more fully in the section titled “Risk Factors” in the Company’s filings with the Securities and Exchange Commission (the “SEC”), including the Company’s annual report on Form 10-K filed with the SEC on February 28, 2023. PROCEPT BioRobotics does not undertake any obligation to update forward‐looking statements and expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward‐looking statements contained herein. These forward-looking statements should not be relied upon as representing PROCEPT BioRobotics’ views as of any date subsequent to the date of this press release.

Important Safety Information

All surgical treatments have inherent and associated side effects. For a list of potential side effects visit https://aquablation.com/safety-information/.

Investor Contact:
Matt Bacso, CFA
VP, Investor Relations and Business Operations
m.bacso@procept-biorobotics.com

To view this piece of content from www.globenewswire.com, please give your consent at the top of this page.
To view this piece of content from ml.globenewswire.com, please give your consent at the top of this page.

About GlobeNewswire by notified

GlobeNewswire by notified
GlobeNewswire by notified
One Liberty Plaza - 165 Broadway
NY 10006 New York

https://notified.com

GlobeNewswire by notified is one of the world's largest newswire distribution networks, specializing in the delivery of corporate press releases financial disclosures and multimedia content to the media, investment community, individual investors and the general public.

Subscribe to releases from GlobeNewswire by notified

Subscribe to all the latest releases from GlobeNewswire by notified by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from GlobeNewswire by notified

IDEX Biometrics 2023 annual report and 2023 executive remuneration report25.4.2024 16:30:00 CEST | Press release

The 2023 annual report and annual financial statements dated 24 April 2024 in pdf as well as ESEF xbrl file format, and also the 2023 executive remuneration report, are enclosed (links below). The financial statements are consistent with the preliminary 2023 statements published on 29 February 2024. The auditor's report includes a matter of emphasis. The reports/files are also available at the company's web site www.idexbiometrics.com For further information contact: Marianne Bøe, Head of investor relations E-mail: marianne.boe@idexbiometrics.com Tel: +47 918 00186 About IDEX Biometrics IDEX Biometrics ASA (OSE: IDEX) is a global technology leader in fingerprint biometrics, offering authentication solutions across payments, access control, and digital identity. Our solutions bring convenience, security, peace of mind and seamless user experiences to the world. Built on patented and proprietary sensor technologies, integrated circuit designs, and software, our biometric solutions target

The Pillar 2 requirement for Aktia decreases by 0.25 percentage points to 1.00%25.4.2024 16:30:00 CEST | Press release

Aktia Bank Plc Insider information 25 April 2024 at 5.30 p.m. The Pillar 2 requirement for Aktia decreases by 0.25 percentage points to 1.00% The Finnish Financial Supervisory Authority has today imposed a discretionary additional capital requirement (Pillar 2) of 1.00% for Aktia Bank Plc Group. The requirement is valid until further notice as of 30 September 2024 but not longer than until 30 September 2027. The current Pillar 2 requirement, valid until the new requirement enters into force, is 1.25%. The Finnish Financial Supervisory Authority’s decision on the Pillar 2 requirement has been made based on the ordinary annual supervisory review and evaluation process (SREP) of credit institutions, based on the Finnish Act on Credit Institutions. The Pillar 2 requirement must be met as follows: at least three quarters of the additional capital requirement shall be Tier 1 capital, of which at least three quarters shall be Common Equity Tier 1 capital (CET1) in accordance with the EU Regul

Buffertkrav enligt prövning för Aktia sjunker med 0,25 procentenheter till 1,00 %25.4.2024 16:30:00 CEST | Pressemelding

Aktia Bank Abp Insiderinformation 25.4.2024 kl. 17.30 Buffertkrav enligt prövning för Aktia sjunker med 0,25 procentenheter till 1,00 % Finansinspektionen har i dag fastställt ett buffertkrav enligt prövning (pelare 2) på 1,00 % för Aktia Bank Abp-koncernen. Kravet gäller tills vidare från och med 30.9.2024, men dock högst till 30.9.2027. Det nuvarande buffertkravet enligt prövning, som gäller fram till att det nya kravet träder i kraft, är 1,25 %. Finansinspektionens beslut om buffertkrav enligt prövning är gjort som en del av den sedvanliga årliga kapitalbedömningsprocessen (SREP) av kreditinstitut, med stöd av kreditinstitutslagen. Buffertkravet enligt prövning ska täckas så att minst tre fjärdedelar av buffertkravet består av primärkapital, varav minst tre fjärdedelar ska bestå av kärnprimärkapital (CET1) enligt EU:s kapitalkravsförordning. Kärnprimärkapitalrelationens minimikrav utgörs av pelare 1- och 2-krav samt av tilläggsbuffertkrav, inkluderande eventuellt systemriskbuffertkr

Former Swedish Country Manager returns to Konsolidator as a Sales Partner25.4.2024 16:28:51 CEST | Press release

Former Swedish Country Manager returns to Konsolidator as a Sales Partner Konsolidator reinforces its focus on the Swedish market by welcoming back former country manager Peter Simonsson as a Sales Partner for Sweden. During his tenure, Peter set a record by securing 90 customers within just 3 years, a testament to his deep understanding of Konsolidator® and the market. Therefore, the potential of this partnership holds a significant promise for Konsolidator’s growth in Sweden. As of April 25, Konsolidator has appointed Peter Simonsson as a Sales Partner, with a specific focus on the Swedish market. With over 25 years of experience in financial consolidation and reporting solutions, Peter brings invaluable expertise in selling these solutions to finance teams in large and small Swedish groups. Additionally, he has led more than 300 financial consolidation and reporting projects, directly engaging with similar software solutions to Konsolidator, catering to the same stakeholders and bus

HiddenA line styled icon from Orion Icon Library.Eye