ADICON Holdings Limited One of the Top Three ICL Service Providers in China is Successfully Listed on Main Board of SEHK

HONG KONG, Jun 30, 2023 – (ACN Newswire) – ADICON Holdings Limited ("ADICON" or "Company", stock code: 9860.HK), one of the top three independent clinical laboratory ("ICL") service providers in China in terms of total revenues during the three years ended 31 December 2020, 2021 and 2022, according to Frost & Sullivan, successfully listed and commenced trading on the Main Board of The Stock Exchange of Hong Kong Limited ("SEHK") today with a board lot size of 500 shares.

Morgan Stanley Asia Limited and Jefferies Hong Kong Limited are the Joint Sponsors, Overall Coordinators, Joint Global Coordinators, Joint Bookrunners and Joint Lead Managers.

ADICON has also entered into cornerstone investment agreements with investors including MR Global (HK) Limited (Mindray), Snibe Diagnostic (Hong Kong) Company Limited, Fosun Diagnostics (Shanghai) Co., Ltd., Timestar Elite Limited and Corelink. Based on the final offer price of HK$12.32 per Offer Share, according to the cornerstone investment agreements, the cornerstone investors have subscribed for a total of 23.647 million shares, accounting for approximately 3.27% of the company's issued share capital immediately after the global offering is completed.

Ms. YANG Ling, Chairwoman and Non-Executive Director of ADICON Holdings Limited, and Managing Director at Carlyle Asia, commented: "ADICON is one of the top three ICL service providers in China and an industry pioneer. Since Carlyle's investment in ADICON in 2018, the Company has transformed from a founder-led business into a corporation that is led by a board of directors and an experienced management team. The successful Hong Kong listing of ADICON today is a recognition of the Company's achievements and I would like to express my sincere gratitude for the trust from the founders, Mr. Lin Jixun and Mr. Lin Feng, and thank and congratulate the management team and everyone at ADICON. We believe the ICL market in China is still in a nascent stage and there remains significant room for the industry to grow. Carlyle will continue to work with the management team and support the Company as it seeks to embark on its next phase of growth."

About ADICON Holdings Limited

ADICON Holdings Limited ("ADICON" or "Company", stock code: 9860.HK) is one of the top three independent clinical laboratory ("ICL") service providers in China in terms of total revenues during the three years ended 31 December 2020, 2021 and 2022, according to Frost & Sullivan. The Company offers comprehensive and best-in-class testing services primarily to hospitals and health check centers through an integrated network of 33 self-operated laboratories across China, as of June 9, 2023. Leveraging its strong R&D and quality control capabilities, ADICON offers comprehensive, high-quality and advanced test portfolios. As of December 31, 2022, ADICON offers a competitive and comprehensive catalog of over 4,000 medical diagnostic tests, including over 1,700 routine tests and over 2,300 esoteric tests, allowing ADICON to provide testing services to over 19,000 customers, ranging from medical institutions, health check centers, to biopharmaceutical companies and CROs. As a market leader in providing ICL services in China, ADICON is committed to continuously serving patients and the general public with its high-quality testing services and becoming a trusted and reliable partner for medical professionals and the general public.

This press release is issued by Porda Havas International Finance Communications Group for and on behalf of ADICON Holdings Limited For further information, please contact:

Porda Havas International Finance Communications Group
Telephone: 852 3150 6788
Email: pearl.hk@pordahavas.com


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

ADICON Announces Proposed Listing on the Main Board of The Stock Exchange of Hong Kong at an Offer Price of HK$12.32 Per Share

HONG KONG, Jun 19, 2023 – (ACN Newswire) – ADICON Holdings Limited ("ADICON" or "Company", stock code: 9860.HK), the pioneer of independent clinical laboratory ("ICL") and one of the top three ICL service providers in China, today announced the proposed listing of its shares on the Main Board of The Stock Exchange of Hong Kong Limited ("SEHK").

Business Highlights
— ADICON is one of the top three independent clinical laboratory ("ICL") service providers in China in terms of total revenues during the three years ended December 31, 2020, 2021 and 2022(1), according to Frost & Sullivan. ADICON believes its success is underpinned by its industry-leading operations, strong R&D and quality-control capabilities, as well as an experienced senior and regional management team.
— ADICON provides comprehensive and best-in-class testing services, primarily to hospitals and health check centers through an integrated network of 33 self-operated laboratories across China.
— ADICON offers a competitive and comprehensive catalog of over 4,000 medical diagnostic tests, including over 1,700 routine tests and over 2,300 esoteric tests. ADICON's testing volume grew at a compound annual growth rate ("CAGR") of 65.6% from 60.1 million in 2020 to 164.9 million in 2022.
— As of June 9, 2023(2), ADICON operates a dedicated cold-chain logistics network covering more than 19,000 customers across 30 provinces and municipalities and over 1,600 cities and counties in China.
— As a market leader in the ICL industry, ADICON is well-positioned to benefit from the growing demand for testing services in China, driven by a series of favorable government policies and industry tailwinds.
— ADICON plans to use the proceeds to drive future growth by enhancing the breadth and depth of its ICL network; continuing to apply innovative technologies to develop new testing methods; further optimizing its laboratory processes and logistics through automation; and selectively pursuing strategic investments and alliances, and other emerging growth opportunities.

Highlights of the Global Offering
— ADICON plans to offer an aggregate of 33,192,500 Offer Shares under the Global Offering (subject to the Over-allotment Option), consisting of 29,872,500 International Offer Shares (subject to reallocation and the Over-allotment Option) and 3,320,000 Hong Kong Offer Shares (subject to reallocation), at a price of HK$12.32 per share.
— ADICON will start its public offering in Hong Kong at 9:00 a.m. on Monday, 19 June 2023, and end at 12:00 noon on Friday, 23 June 2023. Dealings in shares on the Main Board of The Stock Exchange of Hong Kong Limited ("SEHK") are expected to commence on Friday, 30 June 2023, with the stock code of 9860.HK, in board lots of 500 shares each.
— Morgan Stanley Asia Limited and Jefferies Hong Kong Limited are the Joint Sponsors, Overall Coordinators, Joint Global Coordinators, Joint Bookrunners and Joint Lead Managers.

ADICON intends to offer an aggregate of 33,192,500 Offer Shares under the Global Offering (subject to the Over-allotment Option), consisting of 29,872,500 International Offer Shares (subject to reallocation and the Over-allotment Option) and 3,320,000 Hong Kong Offer Shares (subject to reallocation), at a price of HK$12.32 per share. The net proceeds from the Global Offering will amount to HK$480.9 million.

The Hong Kong Public Offering will begin at 9:00 a.m. on Monday, 19 June 2023, and end at 12:00 noon on Friday, 23 June 2023. Dealings in shares on the SEHK are expected to commence on Friday, 30 June 2023, with the stock code of 9860.HK, in board lots of 500 shares each.

ADICON has entered into cornerstone investment agreements with cornerstone investors including MR Global (HK) Limited (Mindray), Snibe Diagnostic (Hong Kong) Company Limited, Fosun Diagnostics (Shanghai) Co., Ltd., Timestar Elite Limited and Corelink, who have agreed to subscribe for such number of the Offer Shares which may be purchased at the Offer Price with an aggregate amount of approximately US$37 million (or approximately HK$290 million).

Mr. GAO Song, Executive Director and Chief Executive Officer of ADICON, stated: "We are committed to adhering to our mission of providing expert medical testing services to all as a market leader in the rapidly growing ICL industry in China. Advanced testing capabilities, innovation and best-in-class quality control standards remain at the core of what we do, and we look to utilize the IPO proceeds to further invest in advanced testing methods and applying innovative technology, as we work to continuously serve as a trusted and reliable partner for medical professionals and the general public."

Ms. YANG Ling, Chairwoman and Non-Executive Director of ADICON, and Managing Director at Carlyle Asia, commented: "We believe the ICL market in China is still in a nascent stage compared to that of other developed countries, and there remains significant room for the industry to grow. As one of the market leaders, ADICON is well-positioned to benefit from this, particularly with its expanding service offerings and strong execution capabilities."

Morgan Stanley Asia Limited and Jefferies Hong Kong Limited are the Joint Sponsors, Overall Coordinators, Joint Global Coordinators, Joint Bookrunners and Joint Lead Managers.

A Market Leader in the Rapidly Growing ICL Industry

Driven by a series of favorable government policies and industry tailwinds, China's ICL market size grew rapidly at a CAGR of 10.9% from RMB14.7 billion in 2017 to RMB22.3 billion in 2021 and is expected to further grow at a CAGR of 18.2% to RMB51.3 billion by 2026, according to Frost & Sullivan. As one of the top three ICL service providers in China, ADICON believes that it is well-positioned to benefit from the growing demand for testing services in China.

ADICON currently offers comprehensive and best-in-class testing services primarily to hospitals and health check centers through an integrated network of self-operated laboratories across China.

— As of the Latest Practicable Date, ADICON has built an extensive service network of 33 self-operated laboratories covering over 30 provinces and municipalities across China.
— ADICON also maintains an industry-leading comprehensive test menu with over 4,000 test items, including over 1,700 routine tests and over 2,300 esoteric tests, allowing the Company to provide testing services to over 19,000 customers by the end of 2022, ranging from medical institutions, health check centers, to biopharmaceutical companies and contract research organizations ("CROs").
— In the past three years, ADICON's testing volume increased by 33.9% from 60.1 million in 2020 to 80.5 million in 2021, and further increased by 104.8% to 164.9 million in 2022.

Aided by the changes implemented by Pearl Group Limited, ADICON's Controlling Shareholders, a company owned by funds which are ultimately controlled by global investment firm, Carlyle, since 2018, ADICON experienced rapid growth and strong financial performance during the Track Record Period. The total revenues grew at a CAGR of 33.1% from RMB2,741.7 million in 2020 to RMB4,860.6 million in 2022. The adjusted EBITDA (non-IFRS measure) grew at a CAGR of 34.0% from RMB567.6 million in 2020 to RMB1,019.8 million in 2022. The adjusted net profit (non-IFRS measure) grew at a CAGR of 30.1% from RMB367.0 million in 2020 to RMB621.1 million in 2022. (3)

ADICON's non-COVID-19 business has also maintained its growth momentum, with revenues totaling RMB1.817 million, RMB2.147 million, and RMB2.576 million in 2020, 2021 and 2022, respectively. With the lift of COVID-19 restrictions in China, demand for the base testing services rebounded, which boosted ADICON's non-COVID-19 revenue growth. Revenue contribution by non-COVID-19 testing business increased significantly from the three months ended March 31, 2022 to the same period in 2023.

Top-Tier and Experienced Management Team Solidified by Shareholder Support

ADICON has assembled a senior management team with in-depth industry insights and extensive experience in global and Chinese healthcare companies and a track record of success which was further bolstered by the addition of Pearl Group Limited, a company owned by investment funds which are ultimately controlled by Carlyle, as ADICON's Controlling Shareholder since October 2018.

The additional resources, expertise and professional management from Pearl Group Limited and other investors have enhanced ADICON's corporate compliance and reset its growth path. The Controlling Shareholders have also provided ADICON with substantial strategic insights and have helped it to strengthen its management capabilities, operational efficiency, business development capabilities, and corporate governance, and have led the Company in its rapid growth and robust track record results.

Comprehensive, High-Quality and Advanced Test Portfolio, Underpinned by Strong R&D and Quality Control Capabilities

ADICON's testing portfolio is at the core of its services: ADICON offers a competitive and comprehensive catalog of over 4,000 medical diagnostic tests as of December 31, 2022, spanning a variety of specialty groups, including among others, clinical immunologic testing, clinical chemistry testing, clinical molecular biology testing, and pathology testing. Its testing portfolio allows the Company to offer a broad spectrum of testing options that facilitate physicians' diagnostic and treatment decisions, and the Company can also customize its test menu to fulfil the specific testing demands from medical institutions, pharmaceutical companies, CROs and other customers.

The comprehensive testing offerings are supported by state-of-the-art laboratories equipped with advanced testing technologies, ranging from chemical analyzers, hematology analyzers, histopathology, flow cytometry, molecular pathology and mass spectrometry to next-generation sequencing (NGS) and digital polymerase chain reaction (dPCR) technologies. Its advanced testing technologies also allow ADICON to efficiently expand into various specialty areas and rapidly develop innovative testing offerings to cater to the evolving clinical needs.

Strong R&D capabilities are the backbone of ADICON's high-quality test offerings: As of the Latest Practicable Date, ADICON owned 228 registered patents, covering its major business focus areas, namely infectious diseases and blood diseases, as well as fields with large and unaddressed clinical demand such as personalized medication, single-gene genetic diseases and solid tumors. ADICON also proactively collaborates with reputable medical research institutions, universities and hospitals to develop new testing methods and technologies to further strengthen its testing capabilities. In addition, ADICON has a dedicated R&D team led by industry veterans who have over 10 years of industry experience and expertise.

Quality control underpins ADICON's abilities to constantly offer high-quality testing services to earn trust and loyalty from its customers: As of December 31, 2022, 18 of ADICON's laboratories were accredited by ISO15189, which enables the Company to provide customers with the assurance that comes with a rigorous global standard. ADICON has established a "headquarters – laboratory" two-level quality assurance system, with all facets of its services subject to stringent quality control standards and measures.

During the Track Record Period, ADICON received over 4,100 external quality assurance ("EQA") certificates. ADICON believes its quality assurance has positioned it strongly to broaden its customer base and capture an increasing market share.

Industry-Leading ICL Operational Capabilities

As an industry leading ICL service provider with a national footprint, ADICON has excellent operational capabilities.

— By the end of 2022, ADICON maintained a robust and nimble logistics network via ground, rail, and air, covering more than 19,000 customers across 30 provinces and municipalities and over 1,600 cities and counties in China. ADICON's logistics capacities ensure speedy transportation of samples and timely reporting of testing results. During the Track Record Period and up to the Latest Practicable Date, ADICON was able to achieve daily same-day delivery of up to 540,000 samples.

— ADICON's effective sales and marketing activities have also helped further fuel its business growth. ADICON has a highly trained and educated in-house sales and marketing team of over 1,500 personnel nationwide, as of December 31, 2022, who actively interact with medical institutions, physicians and key opinion leaders on a regular basis to introduce and promote ADICON's services.

— ADICON also has a specialized sales team of over 200 industry veterans who have extensive knowledge in the relevant specialty areas to promote its esoteric tests. ADICON regularly organizes, sponsors and participates in industry-leading academic conferences, seminars, and symposia to strengthen its brand awareness among medical professionals.

Strong Growth Trajectory Fueled by Expanding Service Offerings and Superior Execution

Network expansion: Supported by a replicable "headquarters – laboratory" two-level management scheme, ADICON has rapidly expanded its footprint nationwide. The number of its laboratories grew from 19 as of December 31, 2018, to 33 as of the Latest Practicable Date, allowing ADICON to serve over 11,000 customers in 2018 to over 19,000 customers in 2022 – ranging from medical institutions and health check centers to biopharmaceutical companies and CROs across 30 provinces and municipalities. Under this scheme, ADICON plans strategies and initiatives centrally and monitors the quality of local executions effectively. The headquarters establishes unified standardized operating procedures and policies which can be carried through and implemented across ADICON's laboratories nationwide, which allows it to open new laboratories and integrate acquired ones cost-effectively and efficiently.

Expanding service offerings: ADICON's test menu has expanded significantly from approximately 1,800 test items in 2018 to over 4,000 test items in 2022. In particular, ADICON's esoteric tests grew from over 650 in 2018 to over 2,300 in 2022. To expand its service offerings continuously, ADICON has entered into partnership agreements with the world's leading and internationally acclaimed companies in the life sciences industry, thus reinforcing its market leadership. In June 2022, the Company entered into a strategic partnership agreement with Guardant Health (Nasdaq: GH), a leading precision oncology company, pursuant to which, the Company is granted the exclusive rights to perform Guardant's industry-leading comprehensive genomic profiling (CGP) tests for researchers in China. ADICON is also the exclusive licensee to process Guardant's proprietary liquid and tissue biopsy assays in China. ADICON also entered into a master lab agreement with a leading global CRO in April 2021, to provide comprehensive, integrated drug development, laboratory and lifecycle management services, and testing services for its designated clinical research study or projects.

Broader customer range: After four years of rapid development, ADICON has significantly expanded its services to all types of medical institutions, health check centers, biopharmaceutical companies and CROs. In April 2019, ADICON started a collaboration with Meinian, a leading health examination and consulting service provider and provided testing services for its health check centers across the country, and soon established a strong presence in the health check market in China. By the end of 2022, ADICON has served a total of over 930 health check centers in China. By leveraging its strong testing capabilities, ADICON also offers testing services to globally and domestically reputable biopharmaceutical companies and CROs, assisting them in streamlining their drug development process and accelerating clinical trials.

Focus On Further Strengthening Its Testing Capabilities and Portfolio to Drive Future Growth

Looking ahead, ADICON plans to leverage the proceeds from this Global Offering to enhance the breadth and depth of its ICL network by strategically penetrating untapped markets; continue to develop new testing methods and apply innovative technologies; further optimize IT infrastructure as well as automate its laboratory processes and logistics; and selectively pursue strategic investments and alliances, and other emerging growth opportunities.

About ADICON Holdings Limited

ADICON Holdings Limited ("ADICON" or "Company", stock code: 9860.HK) is one of the top three independent clinical laboratory ("ICL") service providers in China, which offers comprehensive and best-in-class testing services primarily to hospitals and health check centers through an integrated network of 33 self-operated laboratories across China as of the Latest Practicable Date. Leveraging its strong R&D and quality control capabilities, ADICON offers comprehensive, high-quality and advanced test portfolios. As of December 31, 2022, ADICON offers a competitive and comprehensive catalog of over 4,000 medical diagnostic tests, including over 1,700 routine tests and over 2,300 esoteric tests, allowing ADICON to provide testing services to over 19,000 customers, ranging from medical institutions, health check centers, to biopharmaceutical companies and CROs. As a market leader in providing ICL services in China, ADICON is committed to continuously serving patients and the general public with its high-quality testing services, and becoming a trusted and reliable partner for medical professionals and the general public.

(1) Defined as the "Track Record Period".
(2) Defined as the "Latest Practicable Date".
(3) The use of such non-IFRS measures has limitations as an analytical tool, and they should not be considered in isolation from, or as substitute for analysis of, the results of operations or financial condition of the Company as reported under IFRS.

This press release is issued by Porda Havas International Finance Communications Group for and on behalf of ADICON Holdings Limited For further information, please contact:

Porda Havas International Finance Communications Group
Telephone: 852 3150 6788
Email: pearl.hk@pordahavas.com


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

NSI Lab Solutions Launches MicroVive: The Only 30-Day Rehydration Fluid for Microbiological Cultures

Raleigh, NC, Jun 14, 2023 – (ACN Newswire) – NSI Lab Solutions is excited to introduce MicroVive(TM), the only 30-day rehydration fluid for freezer storage of microbiological-certified reference materials. MicroVive is a single formulation designed to protect bacterial and fungal cell viability during frozen storage for up to 30 days. It is available in either 1.2 or 9 mL pre-proportioned volumes and sold in packs of 20 vials.

MicroVive is perfectly suited for use with NSI Lab Solutions' microbiological-certified reference materials (CRMs) and is the right solution when a laboratory requires multiple cultures to be ready at the same time. Simply place an aliquot of the hydrated inoculum into the MicroVive fluid and store it in the freezer for up to 30 days; frozen samples can then be thawed once for another use.

"We are pleased to add MicroVive to our growing microbiology portfolio," said Evangeline Gonzalez, President, Antylia Diagnostics division. "As we deliver new products for our customers, we are leveraging ZeptoMetrix(R) leadership in new product development. And, with MicroVive, our Certified Reference Materials team is excited to partner with laboratories around the world to maximize workflow flexibility."

More information on how to order new MicroVive and additional NSI Lab Solutions products can be found at https://nsilabsolutions.com/product/microvive/.

Contact Information:
Lauren Stainback
Global Product Manager & Applications Specialist
lauren.stainback@antylia.com

Related Files
NSI Lab Solutions Launches MicroVive.pdf
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Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Asensus Shares First Quarter Results and Future Plans

NEW YORK, Jun 1, 2023 – (ACN Newswire) – PCG Digital — Asensus Surgical, Inc. (NYSE American: ASXC), a medical device company digitizing the interface between the surgeon and the patient to pioneer a new era of Performance-Guided Surgery(TM), recently shared notable operating and financial results for Q1 2023 and significant plans moving forward.



The company reported 20% year-over-year growth in surgical procedures, with more than 900 procedures performed globally during the quarter, and it recently received FDA 510(k) clearance for an expanded indication to treat pediatric patients – in line with a growing commitment to meeting the needs of an underserved pediatric market and connect with key pediatric surgeons.

First quarter revenue was $1 million with cash, cash equivalents, short- and long-term investments, excluding restricted cash, of approximately $57.4 million at the close of the quarter.

Asensus also surpassed 10,000 procedures on its Senhance(R) Surgical System, including a new program launched in Japan – one of the company's fastest-growing regions. The Senhance Surgical System with digital laparoscopy advances minimally invasive surgery with robotic precision.

Asensus' Intelligent Surgical Unit(TM) (ISU(TM)) integrated with the Senhance System is the only real-time solution on the market today that provides surgeons with a suite of tools to use during surgical procedures, including eye tracking camera control, haptic feedback, digital measurement and digital tags. Eye tracking allows surgeons to seamlessly control the camera position without pausing a procedure, and digital tags enhance communication between the surgeon at the console and the OR team website to further engage and support a seamless operating room experience.

Other key accomplishments include:

– Asensus received CE Mark approval for expanded machine vision capabilities on the ISU, which continues to notch praise throughout the industry.

– The ISU recently garnered two prestigious awards: It was named Best New Technology Solution in the MedTech Breakthrough awards' surgical category, where it faced competition from nearly 4,000 nominations across the globe, and Juniper Research Future Digital Awards for Excellence in Digital Health Innovation named Asensus the Best Medical Robotics Solution/Platinum Winner. Both awards are a strong testament to Asensus' commitment to innovation.

– Asensus signed a memorandum of understanding with KARL STORZ, a major player in the surgical device industry. The definitive agreements are progressing towards signing and will represent an important step in expanding commercial reach and development. Upon competition, this will bring the benefits of the ISU to KARL STORZ' extensive global customer base.

– As part of the company's aim to develop pediatric-specific real-world data, a peer-reviewed paper was published detailing the Senhance platform's usage in pediatric procedures. Senhance's unique combination of 3mm instrumentation with a 5mm camera scope combined with haptic feedback make it a unique robotic assisted laparoscopic solution for pediatric surgeries. The surgical team successfully performed surgeries on patients ranging from 4 months to 16 years old, including gallbladder removal, hernia repair, and other types of urological and GI procedures. These early results highlight the potential of the platform in the pediatric population and further validate its safety and effectiveness.

– To better support the pediatric market, Asensus hosted an event with several U.S. pediatric surgeons to gain a stronger understanding of their needs and a subsequent event with a group of key European pediatric surgeons to learn more about supporting further research.

Growth goals and future plans

– For the full year 2023, the Company continues to expect to initiate 10 – 12 new Senhance programs.

– During the second half of 2023, the Company expects to continue initiating integrated system testing for LUNA, the company's next-generation digital surgery platform. Through a combination of advanced minimally invasive instrumentation, the first ever digital interface between the surgeon and the console, and industry-leading clinical intelligence tools, the Company believes the LUNA System is poised to revolutionize the way surgery is performed.

"These are exciting times at Asensus," said Asensus President and CEO Anthony Fernando. "We have continued to push the boundaries of what's possible in robotic surgery, and we will keep pushing to deliver the tools and capabilities that surgeons need to deliver better, more consistent outcomes for their patients."

Disclaimer

This communication was produced by PCG Digital Holdings, LLC, an affiliate of PCG Advisory Inc., (together "PCG"). PCG is not a registered or licensed broker-dealer nor investment adviser. No information contained in this communication constitutes an offer to sell, a solicitation of an offer to buy, or a recommendation of any security. PCG may be compensated by respective clients for publicizing information relating to its client's securities. See www.pcgadvisory.com/disclosures.

PCG Digital
info@pcgadvisory.com
646-863-6341

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Avance Clinical at ASCO & BIO 2023: Early Phase Oncology Trials Increasingly Elaborate and Demand More Patients

ADELAIDE, AUS & SAN DIEGO, May 30, 2023 – (ACN Newswire) – Avance Clinical, the leading award-winning Australian and North American CRO that offers ClinicReady and GlobalReady for early phase biotech companies to speed up the path to regulatory approval, says early phase oncology studies are increasingly more complex and demand more patients. Avance's ClinicReady and GlobalReady service platforms offer significant benefits to product development in oncology.


Avance Clinical's Chief Scientific Officer, Gabriel Kremmidiotis


According to Avance Clinical's Chief Scientific Officer Gabriel Kremmidiotis who is part of the Avance Clinical team attending ASCO:

"Recently, Phase I clinical trial designs in Oncology patients have become more elaborate and include elements of dose escalation, dose expansion and assessment of drug combinations. This, in addition to the increasing number of new emerging therapeutics, has increased the demand for fast progress through the early phases of development and a greater demand for access to patients."

"Utilizing Australia's regulatory environment and high-quality oncology experts, Avance Clinical is able to facilitate a fast project launch and seamless transition across different parts of modular oncology protocol designs. Studies start in Australia and, at appropriate stages, expand to the US as determined by patient accrual number requirements for each study."

"Retaining the majority of backend services (biostatistics, data management, pharmacokinetics and medical writing) in Australia ensures the highest degree of financial benefit for our clients through the Australian R&D tax incentive."

Avance Clinical CEO, Yvonne Lungershausen, Chief Scientific Officer Gabriel Kremmidiotis, and Head of Scientific and Regulatory Affairs Jorgen Mould are featured in a new Global Health video on Reuters news service about the importance of quality clinical trials as part of the drug development process.

The Global Health program brings together 100 leaders and executives from various sectors of the Private and Public Healthcare Industry.

Avance Clinical CEO, Yvonne Lungershausen and Executive VP North American Operations John Mann attended the Global Health Summit and Yvonne was a leading panelist.

Avance Clinical is at the cutting edge of clinical trial technology and has recently been ranked as the world leader in decentralised clinical trials (DCT) technology adoption by GlobalData and Clinical Trial Arena in the CRO sector.

The report found 46% of Avance Clinical's trials incorporated some elements of DCT technologies in 2022 including telemedicine, remote monitoring, and digital data collection. The DCT report also noted that Avance Clinical's staff training in the latest technologies was a key factor in the ranking. See the full report here. https://www.clinicaltrialsarena.com/features/year-in-review-dct-2022/

Avance Clinical's unique GlobalReady offering enables biotechs that have completed early-phase trials in Australia to rapidly and seamlessly transition to the US in preparation for FDA approvals, all with the one CRO and dedicated teams across both regions, which reduces time and cost and delivers quality data.

There are currently more than 280 Phase III global trials that have conducted their Phase I study in Australia, which demonstrates Australian data acceptability with the FDA and other major regulatory authorities. More than 40 biotech clients are now taking advantage of Avance Clinical's GlobalReady program.

This seamless GlobalReady journey is designed so biotechs can:
– Take advantage of the Australian early-phase clinical trial landscape (No IND and 43.5% tax rebate)
– Transition or expand into North America for later phases – without changing CROs (retain study knowledge and processes/team)
– Seamlessly operationalize global dose-escalation and dose-expansion trials across the two regions
– Harness significant speed and cost advantages
– Be assured of quality data – transferable and readily acceptable by the FDA and other regulatory authorities

Book a meeting with Avance Clinical at ASCO https://www.avancecro.com/event/asco-2023-chicago-il/
Book a meeting with Avance Clinical at BIO Booth #2884 https://www.avancecro.com/event/4602/

Find out more:
Learn about the Australian Advantage here https://www.avancecro.com/the-australian-advantage/
For more information about the benefits of running your next study with Avance Clinical
contact us: enquiries@avancecro.com

About Avance Clinical

Avance Clinical is the largest premium full-service Australian and North American CRO delivering quality clinical trials, with globally accepted data, in Australia, New Zealand and the US for international biotechs. The company's clients are biotechs in their drug development phases that need fast, agile, and adaptive solution-oriented clinical research services.

Frost & Sullivan Awards
Avance Clinical, a Frost & Sullivan Asia-Pacific CRO Market Leadership Award recipient for the past three years, has been providing CRO services in the region for more than 24 years.

Pre-clinical through to Phase I and Beyond
Avance Clinical offers pre-clinical consultancy services with their experienced ClinicReady team right through to Phase I and beyond clinical services leveraging significant Government incentive rebates of up to 43.5% and rapid start-up regulatory processes that are available in Australia. With experience across more than 110 therapeutic indications, Avance Clinical can deliver world-class, high-quality, internationally accepted data suitable for FDA and EMA review.

Technology
Avance Clinical uses state-of-the-art technology and gold-standard systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, Zelta, Veeva and Medrio are just some of Avance's technology partners.
www.avancecro.com

Media Contact:
Avance Clinical
Kate Thompson
media@avancecro.com

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Avance Clinical Joins Global Heath Summit Campaign for Faster Access to Life-Changing and Life-Saving Therapies

ADELAIDE, AUS & SAN DIEGO, May 25, 2023 – (ACN Newswire) – Avance Clinical the leading award-winning Australian and North American CRO that offers the programs ClinicReady and GlobalReady for early phase biotech companies to speed up the path to regulatory approval, has been invited to join the Global Health Summit campaign which will be featured on Reuters.



Avance Clinical CEO, Yvonne Lungershausen, Chief Scientific Officer Gabriel Kremmidiotis, and Head of Scientific and Regulatory Affairs Jorgen Mould are interviewed in a new Global Health video featured on Reuters news service about the importance of quality clinical trials as part of the drug development process.

The campaign is a collection of interviews and video documentaries, highlighting international business leaders and healthcare specialists from various industries. The series will showcase organisations spearheading specific health initiatives, developing ground-breaking medicine and complex health technologies, and taking on the challenges of both physical and mental health globally.

The Global Health program launches at the upcoming Global Health Summit on 25-27 May 2023 at the prestigious Intercontinental Hotel in Geneva, bringing together 100 leaders and executives from various sectors of the Private and Public Healthcare Industry.

The event will feature round table discussions where participants will discuss strategies, share knowledge and expertise, and identify opportunities for collaboration. This will be complemented by keynote speeches and panel discussions that will explore the latest trends and emerging issues in the healthcare industry.

Avance Clinical CEO, Yvonne Lungershausen and Executive VP North American Operations John Mann will be attending the Global Health Summit and Yvonne will be a leading panelist. Avance Clinical is at the cutting edge of clinical trial technology and has recently been ranked as the world leader in DCT technology adoption by GlobalData and Clinical Trial Arena in the CRO sector.

The report found 46% of Avance Clinical's trials incorporated some elements of DCT technologies in 2022 including telemedicine, remote monitoring, and digital data collection. The DCT report also noted that Avance Clinical's staff training in the latest technologies was a key factor in the ranking. See the full report here. https://www.clinicaltrialsarena.com/features/year-in-review-dct-2022/

Avance Clinical's unique clinical offering GlobalReady enables biotechs that have completed early to mid-phases in Australia to rapidly and seamlessly transition to the US in preparation for FDA approvals, all with the one CRO and dedicated teams across both regions, which reduces time and cost and delivers quality data.

There are currently more than 280 Phase III global trials that have conducted their Phase I study in Australia, which demonstrates Australian data acceptability with the FDA and other major regulatory authorities.

More than 40 biotech clients are now taking advantage of Avance Clinical's GlobalReady program.

This seamless GlobalReady journey is designed so biotechs can:
– Take advantage of the Australian early-phase clinical trial landscape (No IND and 43.5% tax rebate)
– Transition or expand into North America for later phases – without changing CROs (retain study knowledge and processes/team)
– Seamlessly operationalize global dose-escalation and dose-expansion trials across the two regions
– Harness significant speed and cost advantages
– Be assured of quality data – transferable and readily acceptable by the FDA and other regulatory authorities

Find out more:
– Learn about the Australian Advantage here https://www.avancecro.com/the-australian-advantage/
– Learn about the ClinicReady model here https://www.avancecro.com/about-clinicready/
– Learn about the GlobalReady model here https://www.avancecro.com/avance-clinical-north-america-operations/
or more information about the benefits of running your next study with Avance Clinical
contact us: enquiries@avancecro.com

About Avance Clinical

Avance Clinical is the largest premium full-service Australian and US CRO delivering quality clinical trials, with globally accepted data, in Australia, New Zealand and the US for international biotechs. The company's clients are biotechs in their early phases of drug development that need fast, agile, and adaptive solution-oriented clinical research services.

Frost & Sullivan Awards
Avance Clinical, a Frost & Sullivan Asia-Pacific CRO Market Leadership Award recipient for the past three years, has been providing CRO services in the region for more than 24 years.

Pre-clinical through to Phase 1 and 2
Avance Clinical offers pre-clinical services with their experienced ClinicReady team right through to Phase 1 and 2 clinical services leveraging significant Government incentive rebates of up to 43.5% and rapid start-up regulatory processes. With experience across more than 110 indications, the CRO can deliver world-class results and high-quality internationally accepted data for FDA and EMA review.

Technology
Avance Clinical uses state-of-the-art technology and gold-standard systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, IBM Watson and Medrio are just some of the technology partners.
www.avancecro.com

Media Contact:
Avance Clinical
Kate Thompson
media@avancecro.com

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

EC Healthcare Signs Sustainability-Linked Syndicated Facility, A Ground-breaking Achievement in Hong Kong Healthcare Industry

HONG KONG, May 10, 2023 – (ACN Newswire) – EC Healthcare (the "Company", which together with its subsidiaries is referred to as the "Group", SEHK stock code: 2138), the largest non-hospital medical group in Hong Kong*, is pleased to announce the signing of its first syndicated sustainability-linked loan ("SLL") with a consortium of 5 banks. The SLL was upsized from an initial target of HK$ 700 million to HK$ 1,000 million, demonstrating relationship banks' strong support for the Group and reflecting their confidence in the growth potential of the healthcare industry.

This syndicated SLL, comprising of a revolving credit and term loan, is the first-of-its-kind for a healthcare services provider in Hong Kong. It further enhances the Group's status as a leading industry pioneer and reaffirms the importance of sustainability in the Group's future growth strategy. The proceeds will be used to support the group's expansion plans and working capital needs.

The Mandated Lead Arrangers, Bookrunners and Sustainability Coordinators include The Bank of East Asia, Ltd, The Hongkong & Shanghai Banking Corporation Ltd, and DBS Bank Ltd.

SGS Hong Kong Limited, a leading sustainability consultancy firm, acted as ESG consultant on the SLL to ensure that the new environmental and social targets are aligned with the latest internationally recognized market standards.

Ms. Ada Wong, Executive Director, Chief Strategy Officer & Chief Investment Officer of EC Healthcare said, "This SLL marks another important milestone in the Group's sustainability journey. This transaction recognizes our ongoing ESG efforts and also represents a strong endorsement from the banking community on the Group's business strategy and future growth ambitions. Additionally, the successful arrangement of SLLs in two consecutive years deepens our leadership in terms of sustainable financing in the healthcare sector and reinforces our commitment to sustainability in the long-term."

About EC Healthcare
EC Healthcare is Hong Kong's largest non-hospital medical service provider*, leveraging its core businesses of preventive and precision medicine, and committed to developing medical artificial intelligence by integrating its multi-disciplinary medical services. The move, which is supported by the Group's high-end branding and quality customer services, is aimed at offering customers safe and effective healthcare and medical services with professionalism. The Group is a constituent stock of the Hang Seng Composite Index and the MSCI Hong Kong Small Cap Index.

The Group principally engages in the provision of one-stop medical and health care services in Greater China. The Group provides a full range of services and products under its well-known brands, including those of its one-stop aesthetic medical solutions provider DR REBORN which has ranked first in Hong Kong by sales for years, a professional hair care center HAIR FOREST, primary care clinics jointly established with health management centre re:HEALTH, a vaccine centre Hong Kong Professional Vaccine HKPV, General outpatient clinic Tencent Doctorwork, the largest one-stop pain management centre in Hong Kong New York Medical Group, the comprehensive dental centres Bayley & Jackson Dental Surgeons, EC DENTAL CARE and Health and Care Dental Clinic, an advanced diagnostic and imaging centre HKAI, an oncology treatment centre reVIVE, a day procedure centre HKMED, a specialty clinic PREMIER MEDICAL CENTRE, SPECIALISTS CENTRAL and NEW MEDICAL CENTER, a paediatric centre PRIME CARE, a gynaecology specialist ZENITH MEDICAL CENTER AND PRENATAL DIAGNOSIS CENTRE, PathLab Medical Laboratories, Ophthalmology Center EC EYE and EC Veterinary Hospital and Imaging Center.

*According to independent research conducted by Frost and Sullivan in terms of revenue in 2020 and 2021

For further information, please contact:
iPR Ogilvy Limited
Callis Lau / Lorraine Luk / Tim Tin
Tel: (852) 2136 6952 / 2169 0467 / 3920 7654
Fax: (852) 3170 6606
Email: ech@iprogilvy.com


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Avance Clinical CEO Joins Global BioPharma Panel for Evolution Europe Summit 2023

ADELAIDE, AUS & SAN DIEGO, Apr 18, 2023 – (ACN Newswire) – Avance Clinical the leading award-winning Australian and North American biotech CRO that offers a GlobalReady program to early phase biotech companies to speed up the path to regulatory approval, has been invited to join the Evolution Europe Summit 2023 (Montreux, Switzerland 20 April – 21 April 2023). The panel discussion is focused on the evolution of clinical trials including technology, DCTs, reducing time and cost, drug development planning for approvals, and scaling globally in later phases.

Avance Clinical CEO, Yvonne Lungershausen has been invited to share the Australian and US CRO experience and future projections with a focus on patient centricity and Decentralized Clinical Trials (DCTs) at the Evolution Europe Summit 2023.

Avance Clinical was recently identified by GlobalData as a global leader in DCT technology.

The Evolution Summit is an invitation-only, premium forum bringing leading clinical research executives and innovative solution providers. The summit's content is aligned with key clinical R&D challenges and interests, relevant market developments, and practical and progressive ideas and strategies adopted by successful pioneers. See full details here. https://www.april23.evolution-summit.com/

Avance Clinical has recently been ranked as the world leader in DCT technology adoption by GlobalData and Clinical Trial Arena in the CRO sector. The report found 46% of Avance Clinical's trials incorporated some elements of DCT technologies in 2022 including telemedicine, remote monitoring, and digital data collection.

The DCT report also noted that Avance Clinical's staff training in the latest technologies was a key factor in the ranking. See the full report here. https://www.clinicaltrialsarena.com/features/year-in-review-dct-2022/

Avance Clinical's unique clinical offering GlobalReady enables biotechs that have completed early to mid-phases in Australia to rapidly and seamlessly transition to the US in preparation for FDA approvals, all with the one CRO and dedicated teams across both regions, which reduces time and cost and delivers quality data.

There are currently more than 280 Phase III global trials that have conducted their Phase I study in Australia, which demonstrates Australian data acceptability with the FDA and other major regulatory authorities.

More than 40 biotech clients are now taking advantage of Avance Clinical's GlobalReady program.

This seamless GlobalReady journey is designed so biotechs can:

– Take advantage of the Australian early-phase clinical trial landscape (No IND and 43.5% tax rebate)
– Transition or expand into North America for later phases – without changing CROs (retain study knowledge and processes/team)
– Seamlessly operationalize global dose-escalation and dose-expansion trials across the two regions
– Harness significant speed and cost advantages
– Be assured of quality data – transferable and readily acceptable by the FDA and other regulatory authorities

Find out more:
– Learn about the Australian Advantage here. https://www.avancecro.com/the-australian-advantage/
– Learn about the GlobalReady model here. https://www.avancecro.com/avance-clinical-north-america-operations/
– For more information about the benefits of running your next study with Avance Clinical contact us: enquiries@avancecro.com

About Avance Clinical

Avance Clinical is the largest premium full-service Australian and US CRO delivering quality clinical trials, with globally accepted data, in Australia, New Zealand and the US for international biotechs. The company's clients are biotechs in their early phases of drug development that need fast, agile, and adaptive solution-oriented clinical research services. www.avancecro.com

Frost & Sullivan Awards
Avance Clinical, a Frost & Sullivan Asia-Pacific CRO Market Leadership Award recipient for the past three years, has been providing CRO services in the region for more than 24 years.

Pre-clinical through to Phase 1 and 2
Avance Clinical offers pre-clinical services with their experienced ClinicReady team right through to Phase 1 and 2 clinical services leveraging significant Government incentive rebates of up to 43.5% and rapid start-up regulatory processes. With experience across more than 110 indications, the CRO can deliver world-class results and high-quality internationally accepted data for FDA and EMA review.

Technology
Avance Clinical uses state-of-the-art technology and gold-standard systems across all functional areas to provide clients with the most effective processes. Medidata, Oracle, IBM Watson and Medrio are just some of the technology partners.

Media Contact:
Avance Clinical
Kate Thompson
media@avancecro.com

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

HanchorBio Announces US IND Clearance for the Multi-Regional Clinical Trial of HCB101 to Treat Solid and Hematological Malignancies

TAIPEI, TAIWAN and SAN FRANCISCO, CA, Apr 17, 2023 – (ACN Newswire) – HanchorBio Inc., a global clinical-stage biotechnology company developing innovative immuno-biomedicines, announced today that the US. Food and Drug Administration (FDA) has cleared its investigational new drug (IND) application to initiate a multi-regional clinical trial of its independently-developed novel drug candidate, HCB101, for the treatment of patients with advanced solid tumors or relapsed and refractory non-Hodgkin lymphoma.

Scott Liu, Ph.D., Founder, Chairman, and Chief Executive Officer of HanchorBio, commented, "Although there is demonstrated history of PD-1/PD-L1 immune checkpoint inhibitors showcasing strong efficacy in a variety of cancers and significantly improved the prognosis of certain cancer patients, there is a large percentage of cancer patients who are either refractory to these immunotherapies or develop resistance. HCB101 is our independently-developed leading candidate to block the "do not eat" signal from the SIRPa-CD47 pathway, sufficiently eliminating tumor cells by macrophage while exhibiting excellent safety profile in our preclinical studies. The FDA clearance of our first IND marks a significant milestone for HanchorBio and demonstrates our team's continuous focus and commitment to bringing novel immunotherapies to patients with significant unmet need."

"Based on our studies in 15 murine xenograft tumor models of solid and hematological malignancies, HCB101 has demonstrated superior anti-tumor efficacy, both as monotherapy and in combination with other agents. The advantage is even more apparent when comparing HCB101 with other agents targeting the same pathway currently being investigated in clinical trials," said Sean Juo, Ph.D., President and Chief Scientific Officer of HanchorBio. "Unlike other CD47-blocking agents, HCB101 exhibits excellent safety profiles in the repeat-dose cynomolgus monkey toxicology studies, as no abnormality of RBC or platelet levels were observed. It is an important safety factor for differentiation. I look forward to advancing the clinical development of HCB101 and continuing the focus on patient-centric research and development to hopefully bring novel treatments with clinically meaningful benefits to patients as early as possible."

About HCB101

Using structure-guided protein design and engineering supplemented with relevant screening technologies, HCB101 is an engineered extracellular domain of SIRPa fused to the Fc region of IgG4. HCB101 triggers phagocytic activity of the macrophages by blocking the "do not eat" signal between macrophages and tumor cells. Based on the extensive in-vitro and in-vivo preclinical data, HCB101 is potentially a safer and more potent biologic than the anti-CD47 monoclonal antibodies and SIRPa fusion proteins currently being investigated in clinical trials. Furthermore, quantitative RNA transcriptional analysis indicated that HCB101 triggered distinct gene expression profiles inside the tumor and in the tumor microenvironment comparing to other relevant clinical candidates, suggesting that HCB101 might exhibit unique mechanisms of action.

About Multi-Regional Clinical Trial of HCB101

HCB101-101 is a multi-regional, multi-center, open-label, dose-finding, first-in-human (FIH) study of adults with advanced solid tumors or relapsed and refractory non-Hodgkin lymphoma in the United States and Taiwan. The purposes of the study are to evaluate the safety, tolerability, pharmacokinetics, and clinical anti-tumor activity of weekly HCB101 intravenous injections. The HCB101 IND is on track being reviewed by the Taiwan FDA.

About HanchorBio

Based in Taipei, Shanghai, and San Francisco Bay Area, HanchorBio is a global clinical-stage biotechnology company focusing on immuno-oncology. The Company is led by an experienced team of pharmaceutical industry veterans with proven track-record of success in biologics discovery and global development to transcend current cancer therapies. Committed to reactivating the immune system to fight against diseases, the proprietary Fc-based designer biologics (FBDB(TM)) platform enables unique biologics with diverse multi-targeting modalities to unleash both innate and adaptive immunity to overcome the current challenges of anti-PD1/L1 immunotherapies. The FBDB(TM) platform has successfully delivered proof-of-concept data in several in vivo tumor animal models. By making breakthroughs in multi-functional innovative molecular configurations in R&D and improving the manufacturing process in CMC, HanchorBio develops transformative medicines to address unmet medical needs. For more information, please visit: www.HanchorBio.com or follow us on LinkedIn at www.linkedin.com/company/hanchorbio-inc

Contact Information
Scott Liu
Founder, Chairman and CEO
scott_liu@hanchorbio.com

Yi Du
Sr. Director of Business Development
yi_du@hanchorbio.com

SOURCE: HanchorBio Inc

Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com

Essex and Osteopore Entered into Exclusive Distribution Agreement for Oral Maxillofacial products in Singapore

HONG KONG, Apr 14, 2023 – (ACN Newswire) – Essex Bio-Technology Ltd. ("Essex" or the "Group", Stock Code: 1061.HK) is pleased to announce that its wholly-owned subsidiary, Majeton Pte. Ltd. ("Majeton"), has entered into an exclusive Distribution Agreement with Osteopore Limited ("Osteopore") to promote and sell Osteopore's dental and oral maxillofacial products ("Products") in Singapore.

Pursuant to the Distribution Agreement, Majeton will be the exclusive distributor of the Products for an initial period of 3 years, starting from 2023 to 2026.

Osteopore's innovative oral maxilla facial products are used in guided bone regeneration, immediate implant loading, and socket preservation. In unique situations, Osteopore may also make available customised regenerative implants for various oral maxillofacial reconstruction.

The Group believes that Majeton's strong commercial presence in Singapore, will synergistically bring to market Osteopore's innovative products supported by advanced 3D printing technology for improved clinical outcome in dental patients throughout Singapore's dental clinics, private and public hospitals.

About Osteopore
Osteopore is an Australian and Singapore based medical technology company commercialising a range of bespoke products specifically engineered to facilitate bone healing across multiple therapeutic areas. Osteopore's patented technology fabricates specific micro-structured scaffolds for bone regeneration through 3D printing and bioresorbable material. Osteopore's patent-protected scaffolds are made from proprietary polymer formulations, that naturally dissolve over time to leave only natural, healthy bone tissue, significantly reducing postsurgery complications commonly associated with permanent bone implants.

About Essex (Stock Code: 1061.HK)
Essex Bio-Technology Limited is a bio-pharmaceutical company that develops, manufactures and commercialises genetically engineered therapeutic b-bFGF (FGF-2), having six commercialised biologics marketed in China since 1998. Additionally, it has a portfolio of commercialised products of preservative-free unit-dose eye drops and Shilishun (Iodized Lecithin Capsules) etc.. The products of the Company are principally prescribed for the treatment of wounds healing and diseases in Ophthalmology and Dermatology, which are marketed and sold through approximately 10,900 hospitals and managed directly by its 43 regional sales offices in China. Leveraging on its in-house R&D platform in growth factor and antibody, the Company maintains a pipeline of projects in various clinical stages, covering a wide range of fields and indications.

About Majeton
Majeton, a wholly owned subsidiary of Essex Bio-Technology, is a sales, marketing and distribution company of therapeutics, medical devices and nutraceuticals for the region of South East Asia. The company embraces innovation to provide a portfolio of first-in-class and best-in-class products with the aim to deliver solutions to commercial and clinical unmet needs, covering a wide range of therapeutic areas.

Media Enquiry:
Strategic Financial Relations Limited (Website: http://www.sprg.com.hk)
Shelly Cheng +852 2864 4857 shelly.cheng@sprg.com.hk
Yan Li +852 2114 4320 yan.li@sprg.com.hk
June Tuo +852 2864 4848 june.tuo@sprg.com.hk
Angela Shen +852 2864 4870 angela.shen@sprg.com.hk
Media: media@essex.com.cn

Investor Enquiry:
Investor Relations: investors@essex.com.cn


Copyright 2023 ACN Newswire. All rights reserved. http://www.acnnewswire.com