ROCKVILLE, Md. and SUZHOU, China, Aug. 22, 2024 /PRNewswire/ — Ascentage Pharma (6855.HK), a global biopharmaceutical company engaged in discovering, developing and commercializing both first-in-class and best-in-class therapies for malignancies, today announced its 2024 interim results. During the reporting period, Ascentage Pharma continued to execute its global innovation strategy, having achieved breakthroughs across various aspects of its business including external collaborations, commercialization, and clinical development. In particular, the company has set a new record with its revenue for the first half of 2024 and reported profit for the first time.

• During the reporting period, Ascentage Pharma has set a new record for its revenue that grew by 477% from the same period last year to RMB824 million, with most of the revenue generated from sales of pharmaceutical products and license income. For the very first time in its history, Ascentage Pharma reached profitability, having reported a net profit of RMB163 million.
• Ascentage Pharma made rapid progress with the commercialization of its first approved product, olverembatinib (HQP1351). During the reporting period, olverembatinib generated a sales revenue of RMB113 million, which grew by 120% from the second half of 2023 and 5% year-over-year.
• Ascentage Pharma and Takeda, a multinational pharmaceutical company, have entered into an exclusive option agreement that granted Takeda an exclusive option to enter into an exclusive license agreement for olverembatinib. Once exercised, the Option would allow Takeda to license global rights to develop and commercialize olverembatinib in all territories outside of, among others, the mainland China, Hong Kong China, Macau China, and Taiwan China. Ascentage Pharma has received US$100 million in option payment and a US$75 million equity investment.
• The company’s cash flows continued to improve. As of June 30, 2024, the company’s cash balances were RMB1.1 billion and rose to RMB1.8 billion by early July, 2024.

Entered into a landmark global collaboration that is the largest BD deal among small molecule oncology drugs in China

Ascentage Pharma constantly seeks global partnerships. During the reporting period, the company and Takeda, a multinational pharmaceutical company, entered into an exclusive option agreement for olverembatinib.

This collaboration, with a total value reaching US$1.3 billion, includes an option payment of US$100 million and an option exercise fee and potential milestone payments totaling US$1.2 billion. Additionally, Ascentage Pharma is eligible for tiered double-digit royalties on annual net sales. To date, this is the largest out-licensing deal for any small molecule oncology drug in China. Furthermore, Ascentage Pharma also received an equity investment from Takeda.

This collaboration highlights the significant clinical and commercial potential of olverembatinib in the global market and laid a solid foundation for the future global commercialization of the drug. Ascentage Pharma has already received the US$100 million option payment and US$75 million equity investment from Takeda.

Commercialization of olverembatinib accelerated and strengthened the company‘s revenue generating ability

Following the inclusion of the first approved indication of Ascentage Pharma’s novel drug candidate olverembatinib into the China National Reimbursement Drug List (NRDL) in January 2023 and the regulatory approval for its new indication in November 2023, olverembatinib continued to realize its growth potential while boosting company’s ability to generate revenue through product sales. During the reporting period, the sales revenue of olverembatinib grew by 120% from the second half of 2023 and by 5% year-over-year, to RMB113 million.

Ascentage Pharma is expeditiously expanding the commercialization of its approved product. As of June 30, 2024, olverembatinib has entered 670 hospitals and direct-to-patient (DTP) pharmacies nationwide and its number of listed hospitals has grown by 79% compared to the end of last year. Since the approval of its new indication in November 2023 till June 30, 2024, olverembatinib has been included into 114 supplemental insurance for major diseases and Huimin insurance plans of 20 provinces and 83 municipalities. Additionally, olverembatinib was included into the special drugs catalog of the Huimin insurance plan of 20 provinces and municipalities such as Hebei, Hainan, Inner Mongolia Autonomous Region, Wuxi, Huzhou, Shenzhen, and Yantai, which greatly improved the drug’s accessibility and alleviated the burden on patients.

As the first China-approved third-generation BCR-ABL inhibitor, olverembatinib’s clinical value and therapeutic potential continued to received high profile recognition during the reporting period, both in China and globally. In January 2024, clinical trial results of olverembatinib were included into the US National Comprehensive Cancer Network® (NCCN) Guidelines for the Management of Chronic Myeloid Leukemia (CML). Moreover, olverembatinib has received upgraded recommendations from the 2024 Chinese Society of Clinical Oncology (CSCO) Guidelines for the Diagnosis and Treatment of Hematologic Malignancies in CML and Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL), plus a number of additional Level I recommendations from the guideline.

In July 2024, olverembatinib was approved in Macau China for the treatment of adult patients with tyrosine kinase inhibitor (TKI)-resistant chronic-phase CML (CML-CP) or accelerated-phase CML (CML-AP) harboring the T315I mutation; and adult patients with CML-CP resistant to and/or intolerant of first- and second-generation TKIs, marking another major milestone for olverembatinib following initial approvals it received in the Chinese mainland.

Global innovation strategy yielding more encouraging results with eight registrational studies being simultaneously advanced

Guided by its global innovation strategy, Ascentage Pharma delivered multiple milestone achievements and swiftly advanced its global clinical development programs during the reporting period. To date, two of the company’s key drug candidates, olverembatinib and lisaftoclax (APG-2575), have been cleared to enter 11 registrational studies, including 3 registrational studies that have been completed and 8 registrational studies currently ongoing.

In February 2024, olverembatinib was cleared by the US Food and Drug Administration (FDA) to enter a global registrational Phase III study in previously treated adult patients with CML-CP. This is the first FDA-cleared registrational Phase III study of olverembatinib and it represents a big step forward for Ascentage Pharma’s global clinical development in hematologic malignancies.

Outside hematology, the Center for Drug Evaluation (CDE) of China’s National Medical Product Administration (NMPA) cleared a global registrational Phase III study of olverembatinib in patients with succinate dehydrogenase (SDH)-deficient gastrointestinal stromal tumor (GIST) who had failed prior systemic treatment. This clearance represents a crucial step in Ascentage Pharma’s clinical development in solid tumors.

Meanwhile, Ascentage Pharma also made notable strides with the clinical development of lisaftoclax in hematologic malignancies. During the reporting period, the China CDE cleared a Phase III study of lisaftoclax in combination with azacitidine (AZA) for the first-line treatment of newly-diagnosed patients with higher-risk myelodysplastic syndrome (MDS). This is the fourth cleared registrational Phase III study of lisaftoclax.

Winning recognition from around the world with robust clinical data spanning multiple indications

As an innovative biopharmaceutical company focused on global innovation, Ascentage Pharma has built a high value pipeline composed of assets with first- and best-in-class potentials and conducted more than 40 clinical trials in China, the US, Australia, Europe, and Canada. In this process, Ascentage Pharma made steady progress exploring and validating a number of its drug candidates across multiple indications and presented updated results from its clinical programs at a number of international congresses, showcasing its prowess in R&D and clinical development.

During the reporting period, results from four clinical studies of olverembatinib, lisaftoclax, and APG-2449, the company’s three key drug candidates, were selected for presentations at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting. This is the seventh consecutive year for Ascentage Pharma to present at the meeting. Among these results, the data of olverembatinib in patients with TKI-resistant SDH-deficient GIST were selected for an Oral Report. In the data, olverembatinib showed promising clinical benefit including a clinical benefit rate (CBR) of 92.3% and a median progression-free survival (PFS) of 25.7 months in patients with SDH-deficient GIST, an indication that currently lacks standard of care treatment. At the same meeting, Ascentage Pharma presented the latest data that further demonstrated the therapeutic potential of its FAK/ALK/ROS1 TKI APG-2449 for the treatment of non-small cell lung cancer (NSCLC).

At the 2024 European Hematology Association Hybrid Congress (EHA 2024) which took place in June this year, Ascentage Pharma released update results from five studies of olverembatinib, lisaftoclax, and APG-5918, three of the company’s key drug candidates. These data highlighted the company’s competitiveness in the field of hematologic malignancies. The three studies of olverembatinib presented at EHA 2024 include one that reported the latest median 1-year follow-up data of olverembatinib in patients with CML and Ph+ ALL, updated from the data released at the 2023 American Society of Hematology (ASH) Annual Meeting. In the results, olverembatinib showed excellent durable clinical benefits and favorable long-term tolerability in patients who had been treated with multiple TKIs (including those who were resistant to ponatinib and/or asciminib), regardless of whether they harbored the T315I mutation.

The latest data from multiple studies of lisaftoclax were also selected for presentations at the 2024 ASCO Annual Meeting and EHA 2024. These results highlighted lisaftoclax’ therapeutic potential in a range of hematologic malignancies. Data released at this year’s ASCO Annual Meeting include the latest promising results from a Phase Ib/II study of lisaftoclax in combination with AZA in patients with treatment-naïve (TN) or relapsed/refractory (R/R) acute myeloid leukemia (AML), and a global, multicenter Phase Ib/II study of lisaftoclax alone or in combinations for the treatment of patients with Waldenström macroglobulinemia (WM). At EHA 2024, the company presented encouraging updated data of lisaftoclax in patients with R/R multiple myeloma (MM) or immunoglobulin light-chain (AL) amyloidosis.

Furthermore, results from three preclinical studies of olverembatinib, alrizomadlin (APG-115), APG-2449, and APG-5918 were announced at the 2024 American Association of Cancer Research Annual Meeting (AACR 2024), providing important scientific rationale for the future clinical development of these assets.

Deepening global innovation while opening a whole new chapter on growth and development

To support its long-term strategy and growth, during the reporting period, Ascentage Pharma has confidentially submitted a draft registration statement on Form F-1 to the US Securities and Exchange Commission (SEC) relating to the proposed initial public offering of American depositary shares (ADSs) representing its ordinary shares.

Ascentage Pharma is steadfastly committed to its global innovation strategy and strengthening its intellectual property portfolio. As of June 30, 2024, Ascentage Pharma holds 520 issued patents globally, among of which 367 patents were issued outside of China.

Dr. Dajun Yang, Chairman & CEO of Ascentage Pharma, said, “In the first half of 2024, Ascentage Pharma has achieved multiple milestones in global business development, product commercialization, and global clinical development. These achievements highlight our global innovative capabilities and competitiveness in the field of hematologic malignancies.

During the reporting period, we entered into a global collaboration valued at up to US$1.3 billion with Takeda, a multinational pharmaceutical company, for olverembatinib, in an agreement that also includes tiered double-digit royalties on annual net sales. This is the largest BD deal for any small molecule oncology drug in China. Moreover, we have already received US$75 million in equity investment from Takeda. This collaboration is another validation of our leadership in the industry and olverembatinib’s value in the global market that will hopefully demonstrate clinical potential in more conditions that currently lack treatment options. In February 2024, the US FDA cleared a global registrational Phase III study of olverembatinib, marking yet another major milestone in the global clinical development of the drug.

It is worth emphasizing that during the reporting period, Ascentage Pharma achieved profitability for the first time in its history. With olverembatinib included into the China NRDL and approved for a new indication in the country, we are empowered to further strengthen our commercialization capabilities. At the same time, we made broad progress with our global clinical development programs, expanded the potential indications of our key drug candidates, and reinforced our competitiveness in the field of hematologic malignancies.

Pressing ahead with our patient-centric global innovation strategy, we will continue to build out our commercialization capabilities and accelerate the global clinical development of our investigational assets. To fulfill our mission of addressing unmet clinical needs in China and around the world, we aspire to bring our innovative drugs to the global market as soon as possible for the benefit of more patients around the world and create additional value for societies and our investors.”

About Ascentage Pharma

Ascentage Pharma (6855.HK) is a global, integrated biopharmaceutical company engaged in discovering, developing and commercializing both first-in-class and best-in-class therapies to address global unmet medical needs primarily in malignancies. On October 28, 2019, Ascentage Pharma was listed on the Main Board of the Stock Exchange of Hong Kong Limited with the stock code 6855.HK.

The company has built a pipeline of 9 clinical-stage drug candidates, including novel, highly potent Bcl-2 and dual Bcl-2/Bcl-xL inhibitors, as well as candidates aimed at IAP and MDM2-p53 pathways, and next-generation TKIs. Ascentage Pharma is also the only company in the world with active clinical programs targeting all three known classes of key apoptosis regulators. The company has conducted more than 40 clinical trials in the US, Australia, Europe, and China, including 11 registrational studies (completed/ ongoing/planned).

Olverembatinib, the company’s first lead asset developed for the treatment of drug-resistant chronic myeloid leukemia (CML) and the company’s first approved product in China, has been granted Priority Review Designations and Breakthrough Therapy Designations by the Center for Drug Evaluation (CDE) of China National Medical Products Administration (NMPA). To date, the drug had been included into the China National Reimbursement Drug List (NRDL). Furthermore, olverembatinib has been granted Orphan Drug Designations (ODDs) and a Fast Track Designation (FTD) by the US FDA, and an Orphan Designation by the EMA of the EU.

To date, Ascentage Pharma has obtained a total of 16 ODDs from the US FDA and 1 Orphan Designation from the EMA of the EU for 4 of the company’s investigational drug candidates. Leveraging its robust R&D capabilities, Ascentage Pharma has built a portfolio of global intellectual property rights and entered into global partnerships and other relationships with numerous leading biotechnology and pharmaceutical companies such as Takeda, AstraZeneca, Merck, Pfizer and Innovent; and research and development relationships with leading research institutions such as Dana-Farber Cancer Institute, Mayo Clinic, MD Anderson Cancer Center, National Cancer Institute and the University of Michigan.

The company has built a talented team with a wealth of global experience in the discovery and development of innovative drugs and fully functional commercial manufacturing and Sales & Marketing teams. One pivotal aim of Ascentage Pharma is to continuously strengthen its R&D capabilities and accelerate its clinical development programs, in order to fulfil its mission of addressing unmet clinical needs in China and around the world for the benefit of more patients.

Forward-Looking Statements

The forward-looking statements made in this article relate only to the events or information as of the date on which the statements are made in this article. Except as required by law, Ascentage Pharma undertakes no obligation to update or revise publicly any forward-looking statements, whether as a result of new information, future events, or otherwise, after the date on which the statements are made or to reflect the occurrence of unanticipated events. You should read this article completely and with the understanding that our actual future results or performance may be materially different from what we expect. In this article, statements of, or references to, our intentions and expectations or those of any of our Directors or our Company are made as of the date of this article. Any of these intentions and expectations may alter in light of future development.

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• Bridge Biotherapeutics Enters into a joint research agreement with the Chinese drug discovery platform company “HitGen” to accelerate the discovery of new drug candidates for a FIC novel cancer therapeutics program
• Aims to strengthen its oncology portfolio with a novel drug candidate for newly identified hits from HitGen’s proprietary DEL that are expected to exhibit potent anticancer activity

CHENGDU, China, Aug. 22, 2024 /PRNewswire/ — Bridge Biotherapeutics (“Bridge”, KQ288330), a clinical-stage biotech company, announced that it has entered into a joint research agreement with HitGen Inc. (“HitGen”, SSE: 688222.SH), a Chinese drug discovery platform company. This collaboration builds on successful initial hit finding and identification work from HitGen’s DNA-encoded library (DEL), aiming to further develop the novel hits as promising drug candidates for cancer.

Bridge plans to strengthen its existing oncology portfolio, which is centered on EGFR inhibitors for lung cancer treatment, through new anticancer drug candidates targeting undisclosed targets. Over the past year, the company has established its own analytical methods through preliminary research to discover new targeted anticancer drugs that are expected to show high anticancer effects across various cancer types. With the launch of this joint research with HitGen, it is anticipated that the derivation of effective substances, optimization, and securing of lead compounds will progress rapidly within the next year.

HitGen is a world leader in the development of DEL technology and applications to early-stage small molecule drug discovery. Its platform includes over 1.2 trillion small molecules generated by the DEL technology, and the efficiency of the screening process has made it possible for HitGen to enable drug discovery projects for many organizations around the world. The company has made tremendous improvements over the last few years, making it an integrated drug discovery company focusing on DEL, synthetic therapeutic oligonucleotide (STO), targeted protein degradation (TPD), fragment-based drug discovery and structure-based drug design (FBDD/SBDD).

James Lee, CEO of Bridge Biotherapeutics stated, “By collaborating with HitGen, we will accelerate the discovery of new targeted anticancer drugs.” He added, “We will challenge ourselves to develop drugs that can provide anticancer treatment effects even for genetically mutated cancers, which have been difficult to develop until now.”

Dr. Jin Li, Chairman of the Board and CEO of HitGen Inc., expressed, ” We are pleased to collaborate with Bridge Biotherapeutics team in generating novel drug candidates based on the screening platform we possess,” and stated, “We will contribute to the acceleration of new anticancer drug discovery based on the expertise of both companies.”

Bridge Biotherapeutics has initiated the fourth cohort in the Phase 1 clinical trial for its leading candidate drug BBT-207 for the treatment of non-small cell lung cancer. Through this collaboration with HitGen, the company is embarking on the discovery of new anticancer drugs as part of its efforts to strengthen its cancer portfolio.

About Bridge Biotherapeutics, Inc.

Bridge Biotherapeutics Inc., based in the Republic of Korea and the U.S., is a publicly traded, clinical-stage biotech company founded in 2015. Bridge Biotherapeutics is engaged in the discovery and development of novel therapeutics, focusing on therapeutic areas with high unmet needs, including fibrotic diseases and cancers. The company is developing BBT-877, a novel autotaxin inhibitor for the treatment of fibrotic diseases including idiopathic pulmonary fibrosis (IPF), and BBT-207, a potent targeted cancer therapy for non-small cell lung cancer (NSCLC) with EGFR C797S mutations. Learn more at https://www.bridgebiorx.com/en/.

About HitGen Inc.

HitGen Inc. (SSE: 688222.SH), is a drug discovery research company with headquarters in Chengdu, China, and subsidiaries in Cambridge, UK and Houston, USA. HitGen has established leading technology platforms to enable the discovery and optimization of small molecules and nucleic acid drugs. Our key technology platforms include world-leading DNA-encoded library technology (DEL), fragment-based drug discovery and structure-based drug design technologies (FBDD/SBDD), as well as the emerging technology platforms for synthetic therapeutic oligonucleotide technology (STO), and targeted protein degradation technology (TPD). Through our diverse and flexible business models, we have built up collaboration partnership with several hundred biopharmaceutical research organizations worldwide. HitGen has multiple programmes from early discovery to clinical trial stage. For more information about HitGen, please visit www.hitgen.com.

Source: HitGen Inc.

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Registration is open for the Nov 7-8, Shanghai Meeting

REDWOOD CITY, Calif., Aug. 22, 2024 /PRNewswire/ — Today, the Tianqiao and Chrissy Chen Institute (the Chen Institute) and Science announced that they are holding the second of their annual conference series focused on Artificial Intelligence (AI) and Mental Health in Shanghai, November 7-8, 2024. The meeting is being co-hosted by Shanghai Mental Health Center.

Join us in Shanghai this November for 2024 Chen Institute and Science Joint Conference on AI & Mental Health. Learn more at www.ChenInstitute.org

Mental health is a vast and growing worldwide problem. Because it can affect people at a young age, they will often need treatment and support for many years. During that time, they may be unable to participate at their full potential in society. This explains why, in addition to the suffering experienced by individuals and their families, mental health problems also have an enormous economic and societal impact.

“AI has seen exponential growth and astonishing breakthroughs in recent years, and it has the potential to impact every aspect of modern life and society,” said Chrissy Luo, Chen Institute Co-founder. “Scientists and clinicians are exploring AI’s power for mental health research and treatment and the first results are enormously promising.”

This year’s two-day, English conference will highlight how AI can be used to benefit individuals and society. Over the course of these two days, our speakers will discuss the current state of AI and why we have recently seen such astonishing progress. Global speakers will also review promising applications of AI for the diagnosis and treatment of mental health.

“Science is at the forefront of emerging science and, together with the Chen Institute, we have been closely engaged with scientists and researchers who are unlocking the tremendously powerful potential of using artificial intelligence in the treatment and management of mental health,” said Peter Stern, Senior Editor at Science Magazine.

You can read more about the speakers and their planned presentations here: 
https://www.cheninstitute.org/meetings/2024-ai-and-mental-health

If you live outside of China, you can register here: https://www.eventbrite.com/e/950262128607

If you live in China, please register here: https://app.myhudong.cn/mobile#/microstation_micro?acid=A7vcDJhENbTjupJ3kw&l=a

The Tianqiao & Chrissy Chen Institute was created in 2016 by Tianqiao Chen and Chrissy Luo with a US $1 billion commitment to help advance brain science. The organization’s vision is to improve the human experience by understanding how our brains perceive, learn, and interact with the world. The Institute has a strong focus on artificial intelligence due to its ability to accelerate the pace of scientific research. Read about our AI Prize www.ChenInstitute.org/prize.

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SUZHOU, China, Aug. 21, 2024 /PRNewswire/ — From August 16 to 18, 2024, the judging panel of the International Institute of Artistic Coffee Tasters (IIAC) from Italy, alongside Chinese domestic coffee connoisseurs, gathered at the BeanStar headquarters in Suzhou for the 2024 International Coffee Tasting Competition (ICT), one of the most prestigious events in the global coffee landscape. Over 200 meticulously selected coffee beans from multiple countries underwent a rigorous and discerning tasting process, vying for the coveted accolades in the world of coffee excellence.

Often referred to as the “Oscars” of the coffee world, the ICT is dedicated to discovering the world’s finest coffees, showcasing their exceptional cultivation, meticulous selection, expert roasting, and distinctive originality. The competition’s unwavering commitment to transparency, with blind tasting and data verification under strict sensory analysis rules, positions ICT as the sole competition worldwide that calculates scores on measurable and controllable product attributes. The method eliminates subjective biases, significantly reducing the impact of personal preferences on the outcomes.

The ICT was established by the IIAC in Italy. Since its inception in 1993, the IIAC has emerged as an independent, scientific, and not-for-profit organization, renowned globally as one of the foremost authorities in coffee evaluation. Its pioneering scientific methodology for Italian coffee sensory analysis has garnered widespread acclaim worldwide. Since the first ICT in 2006, the IIAC has received immense respect from the global coffee industry, lauded for its unwavering professionalism, fairness, and transparency in its competition protocols.

The 2023 ICT competition attracted 750 entries from 14 countries, a record achievement. At the event, BeanStar from China alone secured the top score of 98 points, clinching the prestigious Platinum Award. The achievement presents a pivotal opportunity for the ICT to enter into China.

In 2024, the ICT debuted in China, a testament to the rapid expansion of the Chinese coffee market and a steadfast commitment to disseminating scientific coffee tasting methodologies globally. BeanStar, a fast-growing creative coffee brand in China, has been chosen as the first event partner, underscoring the international coffee community’s profound acknowledgment and endorsement of the dynamic growth of China’s coffee industry.

Launched in 2022, BeanStar has established itself as a leader in China’s coffee landscape. Adhering to a strategic blend of quality, creativity, and affordability, BeanStar seamlessly balances the sophistication of boutique coffee with the diverse preferences of mass consumers. In just two years, the brand’s footprint has expanded exponentially, surpassing 200 stores across 36 major Chinese cities and extending its reach internationally with the opening of its maiden outlet in Italy. With an ambitious growth trajectory, BeanStar anticipates surpassing 500 stores by the end of 2024.

BeanStar’s exceptional product quality, unique flavor appeal, and forward-thinking business philosophy have captivated a growing legion of coffee enthusiasts and garnered the favor of renowned capital institutions, including Shunwei Capital, securing three rounds of funding totaling nearly 100 million yuan. As a new force in the global coffee arena, BeanStar’s stellar performance firmly establishes the coffee brewer as a rising star for unprecedented growth and ascendancy.

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• Dedicated VAPM channel on the Docquity platform to support training content for over 2,000 preventive medicine doctors over three years
• The initiative expands Docquity’s community of preventive medicine doctors in Vietnam

HANOI, Vietnam, Aug. 21, 2024 /PRNewswire/ — Docquity, Southeast Asia’s largest healthcare professional (HCP) network, is partnering with the Vietnam Association of Preventive Medicine (VAPM) to enhance medical training for preventive medicine doctors and health staff in Vietnam.

As part of the collaboration, a dedicated VAPM channel has been launched on the Docquity platform, where educational courses, training workshops, and other resources will be developed and rolled out to over 2,000 Vietnamese preventive medicine HCPs during the next three years. Doctors can earn participation certificates by joining these learning sessions. The hub also fosters a conducive environment where VAPM members can engage with each other, share knowledge, and stay informed about the latest advancements in preventive medicine.

The partnership is expected to propel the growth of Docquity’s preventive medicine HCP community in Vietnam, further enhancing the reach and impact of the platform.

Besides providing a robust and secure technological infrastructure, Docquity will work closely with VAPM to ensure the content aligns with Vietnam’s Ministry of Health regulations and guidelines, guaranteeing accuracy, quality, and relevance.

“By partnering with a powerful tech platform like Docquity for the first time, we look forward to reaching and educating more doctors and health staff especially those in remote areas, with greater efficiency and effectiveness,” Prof. PhD. Phan Trong Lan, VAPM’s President, said. “This collaboration will ensure that preventive medicine doctors and health staff across Vietnam have easier access to the latest knowledge and best practices in their field.”

“The partnership between Docquity and VAPM is built on a shared commitment to transform preventive medicine,” Christophe Meugnier, CCO and General Manager of Vietnam & Thailand, Docquity, said. “Our deep healthcare industry insights and innovative digital capabilities uniquely position Docquity to advance how medical  education is delivered to doctors across Southeast Asia. By enabling HCPs to hone their medical expertise and connecting our healthcare enterprise clients with a wider network of doctors, we aim to improve healthcare outcomes across the region.”

For Vietnamese preventive medicine doctors and health staff interested in signing up for VAPM’s learning sessions, please fill in your information here to register for the events and download the Docquity app on Google Play or the Apple App Store to join the learning sessions. The Docquity team will contact you to complete your registration.

About Docquity, https://docquity.com/

Docquity is Southeast Asia’s largest trusted community of verified healthcare professionals. Our vision is to connect healthcare professionals to build healthier lives around the world at scale. Docquity helps healthcare professionals learn, connect, and grow, and partners with companies to reach and educate healthcare professionals as well as provide insights into them.

Docquity has more than 410,000 HCPs on the platform and offices in countries and regions such as India, Indonesia, the Philippines, Malaysia, Singapore, Thailand, Vietnam, and Taiwan. 

About the Vietnam Association of Preventive Medicine

Vietnam Association of Preventive Medicine (VAPM) is a socio-professional, voluntary organization of people who work or are interested in the field of preventive medicine.

The VAPM operates nationwide, according to the law of the Socialist Republic of Vietnam and the Association’s Charter. The Association is under the management of the Ministry of Health of Vietnam and relevant ministries and sectors of the industries and fields in which the Association operates. The Association is a member of the Vietnam General Medical Association.

The Association has its own legal status, seal, symbol and account.

The purpose of the VAPM is to unite its members through the exchange of information, experience, scientific and technical achievements; improve knowledge, professional qualifications and skills in preventive medicine field, contributing to building and developing a modern Vietnamese preventive medicine field; propagating and disseminating scientific knowledge about preventive medicine areas, contributing to raising awareness and changing behavior to protect and improve community health.

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