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A Total of USD 12.7 Million Investment in New Diagnostics and Drug Development for NTDs and Malaria to Partners Including the Ohio State University, PATH, GSK and Others

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TOKYO, Jan. 30, 2025 /PRNewswire/ — The Global Health Innovative Technology (GHIT) Fund announced today a total investment of approximately JPY 2 billion (USD 12.7 million1) in eight projects for the development of new diagnostics and drugs for neglected tropical diseases (NTDs) and malaria.2 

JPY 670 Million (USD 4.2 Million1) Investment in a Critical Diagnostic Tool to Combat Leishmaniasis
There is an estimated 700,000 to 1 million new cases annually of leishmaniasis, an NTD caused by Leishmania parasites transmitted through sandfly bites.3 To advance measures against the disease, the GHIT Fund has decided to invest JPY 670 Million (USD 4.2 Million1) to support a project led by the Ohio State University in collaboration with Nagasaki University and icddr,b, an international health research organization based in Bangladesh. Building on previous research, the project will refine formulations of the leishmanin antigen, conduct pre-clinical safety and efficacy studies, and prepare for regulatory submissions for clinical trials. This project aims to strengthen efforts to monitor infection status and eliminate visceral leishmaniasis. The initiative, driven by global partnerships, is expected to make a significant contribution to tackling NTDs and advancing global health.

The GHIT Fund will also invest in two malaria projects: approximately JPY 680 million (USD 4.2 million1) for the development of a malaria therapeutic drug through a partnership between Eisai Co., Ltd. (Eisai) and Medicines for Malaria Venture (MMV) and approximately JPY 585 million (USD 3.7 million1) for the development of a preventive drug for P. falciparum malaria under the partnership of Program for Appropriate Technology in Health (PATH), GSK Global Health, Eisai and Ehime University.

In addition, the GHIT Fund will invest in the following five screening projects for a total amount of approximately JPY 83 million (USD 0.5 million1):
1) Screening project against malaria by MMV and Daiichi Sankyo Co., Ltd.
2) Screening project against dengue and Zika by Eisai and Drugs for Neglected Diseases initiative (DNDi)
3) Screening project against Lassa fever by MMV and RIKEN
4) Screening project against Rift Valley fever by MMV and RIKEN
5) Screening project against Ebola and Marburg by MMV and RIKEN

Please refer to Appendix 1 for detailed descriptions of these projects and their development stages.

As of January 30, 2025, the GHIT Fund has invested in 37 projects, including 15 discovery projects, 14 preclinical projects and eight clinical trials.4 The total amount of investments since 2013 is JPY 35.8 billion (USD 226 million1) (Appendix 2).

1 USD1 = JPY158.15, the approximate exchange rate on December 30, 2024.
2 These awarded projects were selected and approved as new investments from among proposals to RFP2023-002 and RFP2024-001 for the Product Development Platform and the Screening Platform, which were open for applications from June 2023 to July 2024. 
3 WHO: https://www.who.int/news-room/fact-sheets/detail/leishmaniasis
4 This number includes projects in the registration phase.

The GHIT Fund is a Japan-based international public-private partnership (PPP) fund that was formed between the Government of Japan, multiple pharmaceutical companies, the Gates Foundation, Wellcome, and the United Nations Development Programme (UNDP). The GHIT Fund invests in and manages an R&D portfolio of development partnerships aimed at addressing neglected diseases, such as malaria, tuberculosis, and neglected tropical diseases, which afflict the world’s vulnerable and underserved populations. In collaboration with global partners, the GHIT Fund mobilizes Japanese industry, academia, and research institutes to create new drugs, vaccines, and diagnostics for malaria, tuberculosis, and neglected tropical diseases.
https://www.ghitfund.org/en

Appendix 1. Project Details

ID: G2023-202

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Project Title

Production and pre-clinical testing of cGMP grade Leishmania donovani antigen for Leishmanin skin test (LST)

Collaboration
Partners

  1. The Ohio State University (USA)
  2. Institute of Tropical Medicine at Nagasaki University (NUITM) (Japan)
  3. icddr,b (Bangladesh)

 

Disease

Leishmaniasis

Intervention

Diagnostics

Stage

Pre-clinical

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Awarded Amount

JPY 670,108,468 (USD 4.2 million)

Status

Continued project

Summary

[Project objective]
The objectives of this continuation proposal are to: 1. Produce and characterize cGMP-grade Leishmania antigen (liquid or lyophilized) from L. donovani. 2. Test cGMP leishmanin antigen formulations (liquid and lyophilized) by performing LST in animal models. 3. Perform pre-clinical toxicology studies with cGMP leishmanin antigen formulation that is selected for further advancement based on results from LST studies in animals. 4. Analyze cytokine production in PBMCs or whole blood isolated from healthy individuals and cured VL patients following in vitro stimulation with the selected formulation of cGMP leishmanin antigen. 5. Prepare an IND package for clinical trials. 

[Project design]
During the previous funding period, the project team successfully accomplished goals of the project by 1) optimizing the protocol to produce and scale up production of leishmanin antigen from L. donovani parasites using a cost-effective, scalable and industry suitable osmotic shocklysis technique; 2) performed stability studies; 3) validated GLP leishmanin antigen using experimental animal models, and 4) completed manufacturing of cGMP cell bank of L. donovani at ATCC. In this project, three different formulations of leishmanin antigen will be produced from cGMP L. donovani cell bank. The formulations will be validated for safety and potency using preclinical animal models of vaccination and cured VL. One formulation will be selected for further advancement and scale-up of cGMP production on the basis of results from stability studies and LST studies in animals, and pre-clinical toxicology studies will be performed as per regulatory guidelines. To assess the immunogenicity of the product, cytokine production in PBMCs or whole blood isolated from healthy individuals and cured VL patients following in vitro stimulation with the selected formulation of cGMP leishmanin antigen will also be analyzed. IND package will be prepared for submission to regulators for clinical trials.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/226/en

ID: G2024-114

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Project Title

Lead optimization and preclinical studies of new antimalarial Gwt1p-inhibitors with a novel mechanism of action, improved efficacies and safety profiles

Collaboration
Partners

  1. Eisai Co., Ltd. (Eisai) (Japan)
  2. Medicines for Malaria Venture (MMV) (Switzerland)

 

Disease

Malaria

Intervention

Drug

Stage

Lead Optimization

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Awarded Amount

JPY 680,010,000 (USD 4.3 million)

Status

Continued project

Summary

[Project objective]

The objective of this proposal is to investigate the new Gwt1p-inhibitor and find a back-up candidate with improved activity and safety profile. To deliver this goal, the project team will focus on the following specific objectives:

(1) Two chemical series will be chemically optimized and a frontrunner compound will be selected from each series, as precandidates.

(2) Two precandidates will be evaluated in multiple assays and the most favorable compound will be selected as a Late Lead.

(3) The synthetic route of Late Lead will be optimized and GLP manufacturing will be conducted.

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(4) Non-rodent DRF study will be conducted and candidate selection will be scheduled following a successful outcome to this study.

[Project design]
In this project, chemical modification of two lead series will be conducted to improve anti-Plasmodium activity and safety profile while securing a long-half-life. Synthesized new compounds will be shipped to Eisai’s Tsukuba Research Laboratories in Japan. They will be tested according to the defined screening cascade starting from the primary screening of anti-Plasmodium activity and cytotoxicity. Compounds which show good anti-Plasmodium activity and safety margin will be tested for solubility at neutral pH and stability against human and murine liver microsomes assays. Based on these results and other profiling, the most promising compound in each series will be selected as pre-candidate and will be further evaluated. Two precandidates will be evaluated in the in vitro/vivo anti-Plasmodium assay, a rat dose range finding (DRF) study, safety profiling, human dose prediction, salt selection, resistant risk assessment and parasite life-cycle assays. The most favorable compound will be selected as a Late Lead. The synthetic route for the Late Lead will be optimized and GLP manufacturing will be conducted. Non-rodent DRF study using the manufactured GLP material will also be conducted. The final goal of this project is the candidate selection in both Eisai and MMV and planned for September 2026.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/227/en

ID: G2023-219

Project Title

Manufacture of clinical trial material for a monoclonal antibody to prevent P. falciparum malaria

Collaboration
Partners

  1. Program for Appropriate Technology in Health (PATH) (USA)
  2. GlaxoSmithKline Investigacion y Desarrollo, S.L. (Spain)
  3. Eisai Co., Ltd. (Eisai) (Japan)
  4. Ehime University (Japan)

 

Disease

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Malaria

Intervention

Drug

Stage

Pre-clinical

Awarded Amount

JPY 585,190,112 (USD 3.7 million)

Status

Continued project

Summary

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[Project objective]

The objective of this project is to complete GMP drug substance and GMP drug product manufacturing to support the future Investigational New Drug Application (IND) submission to the United States Food and Drug Administration (US FDA) for a proof-of-concept clinical trial that includes controlled human malaria infection. Our long-term goal is to secure a WHO recommendation for a mAb that prevents P. falciparum malaria in young children living in areas of seasonal transmission in sub-Saharan Africa.

[Project design]
The project is built on our successful completion of the following activities: 1) production and release of a pre-master cell bank for the candidate mAb; 2) development and optimization of the manufacturing process for the candidate mAb to confirm production conditions for Good Laboratory Practice toxicology studies and future scale-up; 3) formulation development to enable stability of the mAb at a high concentration to accommodate potential subcutaneous injection; and 4) a pre-IND meeting with the US FDA on the proposed nonclinical and clinical program, specifically on the adequacy of the nonclinical toxicology studies to support the FIH Phase 1 study.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/228/en

ID: S2024-111

Project Title

Hit Validation of novel Daiichi Sankyo compounds with antimalarial activity

Collaboration
Partners

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  1. Medicines for Malaria Venture (MMV) (Switzerland)
  2. Daiichi Sankyo Co., Ltd. (Japan)

 

Disease

Malaria

Intervention

Drug

Stage

Screening

Awarded Amount

JPY 4,000,000 (USD 25,292.44)

Status

Continued project

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Summary

[Project objective]

The objective of the Hit Validation project is the synthesis and testing of a small array of compounds designed to investigate the minimum pharmacophore, key structural features required for activity and scope to address issues identified through the profiling of the hits identified from the earlier HTS campaign (S2020-113). If a compelling data package is obtained and the series clear potential for further development towards an Early Lead, a GHIT HTLP proposal will be submitted.

[Project design]
The focus of the array of analogs is to explore the key features required for activity and scope to address potential issues. A feature of the overall design of the array is focused on modifications with potential to improve the metabolic stability of the series in line with potential to deliver a long duration antimalarial (predicted human T1/2 > 120 h). The lipophilicity of the analogues covers a range of values from approximately 1.5 to 4.5 which will help to identify if data (potency, metabolism, cytotoxicity, etc.) correlates with either LogP or LogD.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/229/en

ID: S2024-123

Project Title

Exploration of Novel Antiviral Compounds for the Development of Therapeutics Against Flavivirus Infections

Collaboration
Partners

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  1. Eisai Co., Ltd. (Eisai) (Japan)
  2. Drugs for Neglected Diseases initiative (DNDi) (Switzerland)

 

Disease

Dengue and Zika

Intervention

Drug

Stage

Screening

Awarded Amount

JPY 12,653,193 (USD 80,007.54)

Status

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New

Summary

[Project objective]

The project team aims to identify hit compounds that will serve as the starting point for new drug development by exploring novel compounds that exhibit antiviral activity against flaviviruses such as dengue virus and Zika virus.

[Project design]
To explore compounds that exhibit antiviral activity against dengue virus and Zika virus, the project team will screen two types of compound libraries, a focused library and a diversity library, using an image-based phenotypic assay system. In the phenotypic assay system, viral proteins and host cell nuclei are stained, and the antiviral activity of the compounds is determined by analyzing fluorescent confocal images. The focused library consists of compounds selected by a machine learning model developed using assay data accumulated by Eisai. By complementarily utilizing the diversity library, the project team efficiently explores compounds that exhibit antiviral activity. Ultimately, the project team aims to identify hit compounds that show activity against dengue virus and Zika virus to establish preliminary structure-activity relationships, physicochemical properties, and other relevant biological information.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/231/en

ID: S2024-113

Project Title

Screening Project between RIKEN and MMV

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Collaboration
Partners

  1. Medicines for Malaria Venture (MMV) (Switzerland)
  2. RIKEN (Japan)

 

Disease

Lassa Fever

Intervention

Drug

Stage

Screening

Awarded Amount

JPY 20,064,000 (USD 126,866.90)

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Status

New

Summary

[Project objective]

The project aims to use a cell-based, infection-free platform to identify potential treatments against LASV using the RIKEN NPDepo library. Additionally, the project seeks to study the effectiveness of selected confirmed treatments against lymphocytic choriomeningitis virus (LCMV), Tacaribe virus (TCRV), and Junin virus (JUNV) in order to identify potential broad-spectrum antiviral compounds. This collaboration leverages the screening capabilities and drug development expertise of Japan’s largest comprehensive institution, PDP, and academic investigators to achieve its goals.

[Project design]
The primary screen will use LASV-vRNP/293mRFP to assess a subset of the RIKEN NPDepo library. The screen will be in a 384-well plate format with a single compound concentration of 10 µM. Compounds will be evaluated for their antiviral activity and impact on cell viability. Approximately 200 compounds will be selected for further confirmation studies based on specific criteria. Confirmed actives will undergo broad-spectrum antiviral testing and prioritization for further profiling. Selected hits meeting specific criteria will be considered for future development.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/232/en

ID: S2024-114

Project Title

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Screening Project between RIKEN and MMV

Collaboration
Partners

  1. Medicines for Malaria Venture (MMV) (Switzerland)
  2. RIKEN (Japan)

 

Disease

Rift Valley fever

Intervention

Drug

Stage

Screening

Awarded Amount

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JPY 23,712,000 (USD 149,933.61)

Status

New

Summary

[Project objective]

The project aims to use a live virus platform to identify potential compounds active against the Rift Valley fever virus (RVFV) using the RIKEN NPDepo library. Furthermore, the project intends to investigate the activity of selected compounds against the Punta Toro virus and La Crosse virus in order to identify potential broad-spectrum anti-bunyavirus compounds. This collaboration leverages the screening capabilities and drug development expertise of Japan’s largest comprehensive research institution, PDP, and academic investigators to achieve its goals.

[Project design]
The initial screening will involve using the MP-12 strain of RVFV to infect human hepatocyte cells. A subset of the RIKEN NPDepo library (20,000 compounds) will be screened in a 384-well plate with a single compound concentration of 10 µM. The results will be evaluated for antiviral activity and cell viability, and potential hits will be chosen based on specific criteria.

About 100 compounds (assuming a 0.5% hit rate) will be selected from the screening for further confirmation studies. These studies will involve testing the compounds at three different doses in cultured cells infected with RVFV, similar to the initial screen, and assessing cytotoxicity. From the confirmed compounds, RIKEN and MMV will prioritize up to 5 hits for further evaluation.

To assess the potential for broad-spectrum anti-bunyaviral activity, the confirmed compounds will be tested against Punta Toro virus and the more distantly related La Crosse virus.

The hit series meeting MMV and GHIT criteria for further development (hits with confirmed EC50 < 5 µM against live viruses and a selectivity index (SI = CC50/EC50) of ≥10, with progressable chemotypes) will form the basis of a future GHIT HTLP application. 

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Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/233/en

ID: S2024-115

Project Title

Screening Project between RIKEN and MMV

Collaboration
Partners

  1. Medicines for Malaria Venture (MMV) (Switzerland)
  2. RIKEN (Japan)

 

Disease

Ebola and Marburg

Intervention

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Drug

Stage

Screening

Awarded Amount

JPY 22,800,000 (USD 144,166.93)

Status

New

Summary

[Project objective]

The project aims to use a multi-filovirus “rainbow” system that can simultaneously test for EBOV, MARV, and SUDV using a single cell line to identify potential treatments against filoviruses using the RIKEN NPDepo library. Additionally, the project seeks to study the effectiveness of selected confirmed hits against other filoviruses (Tai Forest, Reston, Bundibogyo, Lloviu) in order to identify potential broad-spectrum antiviral compounds. This collaboration leverages the screening capabilities and drug development expertise of Japan’s largest comprehensive institution, PDP, and academic investigators to achieve its goals.

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[Project design]
The primary screen will be performed on a subset of the RIKEN NPDepo library (20,000 compounds). The screen will be in a 384-well plate format with a single compound concentration of 10 µM. Compounds will be evaluated for their antiviral activity and impact on cell viability. Approximately 200 compounds will be selected for further confirmation studies based on specific criteria. Confirmed actives will undergo broad-spectrum antiviral testing and prioritization for further profiling against live Ebola virus. Selected hits meeting specific criteria will be considered for future development.

Project Detail

https://www.ghitfund.org/investment/portfoliodetail/detail/234/en

*All amounts are listed at an exchange rate of USD1 = JPY158.15, the approximate exchange rate on December 30, 2024.

Appendix 2. Investment Overview (as of January 30, 2025)

Investments to date
Total investments: 35.8 billion yen (USD 226 million1)
Total invested projects: 133 (37 active projects and 96 completed projects)
To learn more about the GHIT Fund’s investments, please visit
Investment Overview: https://www.ghitfund.org/investment/overview/en
Portfolio: https://www.ghitfund.org/investment/portfolio/en
Advancing Portfolio: https://www.ghitfund.org/investment/advancingportfolio/en
Clinical Candidates: https://www.ghitfund.org/investment/clinicalcandidates/en

For more information, contact:
Katy Lenard at +1-202-494-2584 or klenard@burness.com
Mina Ohata at +81-36441-2032 or mina.ohata@ghitfund.org

View original content:https://www.prnewswire.co.uk/news-releases/a-total-of-usd-12-7-million-investment-in-new-diagnostics-and-drug-development-for-ntds-and-malaria-to-partners-including-the-ohio-state-university-path-gsk-and-others-302363864.html

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Alis Biosciences launches fund to free over USD$30 billion of capital trapped in listed development-stage life sciences and biotech companies

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  • Significant market inefficiencies have left over USD$30 billion of capital trapped in c.300 listed biotech companies worldwide that have experienced clinical or regulatory setbacks
  • Fund provides efficient mechanism to help investors recoup and recycle trapped cash, while allowing residual science and IP to be developed
  • Fund to be listed on public markets in due course
  • Led by highly experienced industry and investment executives Annalisa Jenkins and Nicholas Johnston

LONDON, April 18, 2025 /PRNewswire/ — Alis Biosciences (“Alis”), an investment fund focused on returning capital to investors that is currently trapped in listed, development-stage biotech companies, today formally launches. Founded by highly experienced industry and investment executives, Alis’ goal is to protect public shareholders’ funds while still supporting company management and boards.

Currently, there are nearly 300 listed, development stage life sciences and biotech companies worldwide that have experienced clinical, regulatory or commercial setbacks. These have trapped capital worth over USD$30 billion on their balance sheets, with market caps ranging from USD$5 million to USD$100 million and cash reserves ranging from USD$10 million to USD$400 million.

Alis offers public companies a range of innovative and adaptable structures to return capital to their shareholders, while providing a chance for any residual science and IP to be developed if appropriate.   Alis will approach the board and management of each target company and mutually agree the optimum Alis structure to deploy. Alis will then seek to delist the company from the public market with the agreement of its shareholders in the normal way. Each delisted company’s cash and IP will be held in individual Special Purpose Vehicles (“SPV”) which are managed by Alis. Applicable cash will then be returned to shareholders immediately, with the IP either developed or sold using one of the following structures.

  • Structure A returns most of the uncommitted cash to shareholders (e.g. 97%), with the company then sold back to certain shareholders or stakeholders who wish to further develop any residual science. Alis will retain a small stake with any upside from its stake shared across these shareholders.
  • Structure B returns the vast majority of uncommitted cash to shareholders (e.g. 95%), leaving just enough to manage the structured wind-down of the company. Alis keeps the IP associated with this company. This process will be far quicker than any bankruptcy process.

In the near term, Alis will seek a public market listing that will allow it to offer a further Structure:

Structure C leaves enough cash in the acquiring vehicle (e.g. 40% of cash balance), to allow Alis to fund further clinical programmes, with the remaining 60% of cash immediately returned to shareholders along with an equity interest in Alis. The proceeds from any clinical success will then be retained by participating contingent value rights and by retaining shares in Alis.

Nicholas Johnston, Board Member and Founder of Alis Biosciences, commented: “We founded Alis Biosciences to alter the status quo, where tens of billions of dollars of investors’ funds are trapped in moribund listed life sciences and biotech companies. Our highly experienced team work collaboratively with shareholders, management, and boards, to provide the optimum mechanism to return capital to shareholders, while also allowing stakeholders the option to further develop residual science and IP where there is potential to do so. This is too big a problem to ignore and Alis is committed to providing a fresh solution.”

Annalisa Jenkins, Chair of Alis Biosciences added: “In this challenging financial market environment, there is a need for greater creativity to find answers to this USD$30 billion problem. This needs to be solved if capital is to be effectively recycled within the capital market ecosystem to finance exciting new science that has the potential to succeed and deliver investor returns. 

“Public and private investors have expressed strong support for Alis Biosciences’ tailored approach, reflecting demand for a new solution to this longstanding problem. We firmly believe that our highly experienced and scientifically knowledgeable investment team can not only help to return value to shareholders but also develop any viable residual science. 

Frequently, following a clinical or regulatory set back, publicly listed life sciences and biotech companies experience an often immediate and sharp decline in their stock price, coupled with the immediate and consequent loss of stock liquidity. This leaves cash on their balance sheet far in excess of their current market capitalisation, no commensurate growth or limited alternative near-term clinical development prospects of success, and no efficient and timely mechanism to return cash to shareholders.  

These companies often hope to develop another compound or product in their pipeline or merge with a private company, thereby heavily diluting shareholder equity. These alternatives typically have a very different investment case from the original programme, but investors are left with no option but to follow the direction of management or the board, while tens of millions of dollars of investor capital remains on the balance sheet. Even when a company files for bankruptcy, this process is time consuming and expensive, and further delays the return of any cash to shareholders while failing to adequately capture any residual value in the company’s IP.

About Alis Biosciences

Alis Biosciences (“Alis”) is an investment fund focused on returning capital to investors that is currently trapped in listed, development-stage biotech companies. Alis protects the interests of acquired company shareholders by providing a mechanism to return capital and resuscitate viable science, creating a novel and much-needed market safety net that may end up boosting investment in high tech healthcare.

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Significant market inefficiencies have left over USD$30 billion of capital trapped in c.300 biotechs all of which have experienced setbacks – typically a failure in clinical trials of their lead programme or unsuccessful commercial launch. Following a sharp decline in their stock price, with the concurrent reduction in liquidity, these companies are left with cash on their balance sheet far in excess of their market capitalization, no commensurate growth or limited alternative near-term clinical development prospects of success; and importantly with no efficient and timely mechanism to return cash to shareholders.

Alis has a highly experienced and scientifically knowledgeable team that works collaboratively with shareholders, management, and boards. It has a flexible approach, with different innovative structures, all adaptable, which provide a mechanism to return capital to shareholders, while also allowing stakeholders the option to further develop residual IP if enough stakeholders, in collaboration with external advisors, suggest there is potential.

Multiomic analysis will be used to validate the residual IP within companies to determine whether a positive outcome is achievable. The feedback from this work, carried out over a relatively short period of time, will then be used to determine whether a different path forward is possible for any of the residual IP left within a particular company.

For more information, please visit: www.alisbiosciences.com

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Xlence Introduces Xlence Academy to Help Traders Learn and Grow

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https://www.xlence.com

DUBAI, UAE, April 18, 2025 /PRNewswire/ — Xlence, an international CFD broker with an expanding presence in, MENA, and Asia, officially launched the Xlence Academy, a multilingual teaching portal for traders to study forex concepts and trading tactics.

 

 

The Xlence Academy was established to deliver education that efficiently fosters trader development. This is backed by practical, expert-oriented courses that are not solely theoretical but applicable at all levels.

Structured Learning for Traders at Every Level

Aiming at the rising demand for clear, practical teaching, the Xlence Academy offers an educational system that guides traders from fundamental concepts to advanced strategies. The Academy helps users start trading or improve their skills by promoting long-term skill development to build confidence and security in learning.

Key Features of the Xlence Academy:

  • Introduction to Forex
    Covering execution, order classifications and currency pairs, it covers the principles of the forex market.
  • Fundamental Analysis
    Learn how to include economic data, central bank policies, and world news in trading decisions by understanding how they affect market behaviour and present trading opportunities.
  • Technical Analysis
    Investigate price action techniques, technical indicators, and chart patterns to allow you to define entry and exit positions.
  • Trading Strategies
    Develop confidence with methodical strategy courses on risk management, trend tracking, and breakout approaches for different market situations.

More Than Education: A Foundation for Success

The Academy offers a reliable foundation based on expert knowledge and practical application in a market setting where trading errors can be expensive.

The Academy helps traders foster the psychological discipline and risk awareness required to succeed, in addition to technical proficiency, by providing a systematic path from beginner to advanced levels. This all-encompassing approach reflects Xlence’s principle that comprehension, consistency, and ongoing learning are the foundations of long-term success.

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 Xlence gives traders the tools to take charge of their journey, make wiser choices, and interact with international markets from a strong position through the Academy.

About Xlence

Xlence is an international CFD broker focused on delivering a comprehensive trading experience through transparency, innovation, and global market access. With a significant footprint across, MENA, and Asia, it strives to meet the diverse needs of contemporary traders while upholding the highest ethical standards.

For more information, visit www.xlence.com and explore our free educational resources to support your trading success. We encourage you to take advantage of these resources and start your journey towards becoming a more informed and strategic trader.

Trade with Xlence, Excel in Trading

All trading involves risk. It is possible to lose all your capital. You should consider whether you can afford to take the high risk of losing your money.

Logo: https://mma.prnewswire.com/media/2606624/Xlence_Dark_Logo.jpg

Media contact:
Nicolas Georgiou 
info@xlence.com 
+357 96199856

Cision View original content:https://www.prnewswire.co.uk/news-releases/xlence-introduces-xlence-academy-to-help-traders-learn-and-grow-302431399.html

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CGTN: Head-of-state diplomacy promotes ironclad friendship between China and Cambodia

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CGTN published an article highlighting how Chinese President Xi Jinping’s visit has promoted the ironclad friendship between China and Cambodia, the fruitful results in economic and trade cooperation between the two countries, and how cultural exchanges boost ChinaCambodia ties.

BEIJING, April 18, 2025 /PRNewswire/ — China and Cambodia set a model for equality, mutual trust and win-win cooperation between countries of different sizes, Chinese President Xi Jinping said on Thursday while meeting with Cambodian King Norodom Sihamoni during his state visit to Cambodia.

Xi said he believes Chinese modernization will bring more opportunities to neighboring countries, including Cambodia, noting that building a ChinaCambodia community with a shared future is a choice of history and the people.

ChinaCambodia relations have withstood the test of global transformations and have always remained rock-solid. The bilateral ties were forged and nurtured by the older generation of leaders of the two countries.

In February 2023, during the then Cambodian Prime Minister Hun Sen’s visit to China, the two sides agreed to develop a “diamond cooperation framework” with six priority areas: political cooperation, production capacity and quality, agriculture, energy, security, and people-to-people exchanges.

In September 2023, Hun Manet chose China as his first official overseas destination after assuming office as Cambodia’s prime minister. During his meeting with Chinese President Xi Jinping, Hun Manet pledged to further carry forward the ironclad friendship between Cambodia and China.

In May 2024, a road in Phnom Penh was named “Xi Jinping Boulevard” by the Royal Government of Cambodia to honor the Chinese leader’s historic contributions to the country’s development. At the naming ceremony, Hun Manet highlighted that bilateral ties have entered their best period in history under the leadership and joint efforts of Xi and Cambodian leaders.

Fruitful results in economic and trade cooperation

First, two-way trade has expanded remarkably thanks to the Regional Comprehensive Economic Partnership (RCEP) free trade deal and the China-Cambodia Free Trade Agreement (FTA). China has been Cambodia’s largest trading partner for 13 consecutive years. And in 2024, two-way trade reached $17.83 billion, up by 20.7 percent year-on-year.

The approval for high-quality Cambodian agricultural and fishery products such as rice, bananas, mangoes, longans, coconuts and basa fish to enter the Chinese market has not only graced the dining tables of Chinese consumers but also boosted the incomes of Cambodian people.

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Second, investment cooperation has continued to deepen. China has remained Cambodia’s largest source of foreign investment for 13 consecutive years, with investments spanning a wide range of sectors, including transportation, power, agriculture, manufacturing, tourism, special economic zones, as well as information and communications technology, characterized by extensive coverage, large scale and strong results.

About 95.4 percent of the Cambodian respondents have a positive attitude toward Chinese companies investing or operating in Cambodia. And 95 percent believe that China has made positive contributions to the development of the world economy, according to a recent CGTN poll. 

Cultural exchanges boost ChinaCambodia ties

In addition to political and economic cooperation, the two countries have set an example in conducting cultural exchanges, which not only strengthen mutual understanding but also draw closer bonds between the two peoples.

ChinaCambodia people-to-people exchanges, as a key pillar of ChinaCambodia friendship and cooperation, were boosted by the China-Cambodia People-to-People Exchange Year 2024.

Over the years, the medical cooperation programs, including “Love Heart Journey,” “Bright Journey” and “Smile Journey,” have provided quality health care service to grassroots populations in more than 20 Cambodian provinces and cities.

As a cultural bridge between the two countries, the Confucius Institute has also provided free Chinese courses to more than 100,000 Cambodian learners since its establishment in Cambodia in 2009.

The cultural exchanges between the two countries are expected to continue to expand under the guidance of the China-proposed Global Civilization Initiative, which will benefit areas ranging from culture, youth, media, think tanks, tourism, and technology to healthcare and cultural relics restoration.

“Let us have more frequent people-to-people exchanges. We should uphold solidarity and harmony, have more cultural dialogues, increase experience sharing on state governance, expand diverse forms of cooperation in areas of culture, tourism, youth exchange and protection and restoration of cultural heritages, and promote people-to-people connectivity,” Xi said in a signed article ahead of his arrival in Cambodia for a state visit.

https://news.cgtn.com/news/2025-04-17/Head-of-state-diplomacy-promotes-China-Cambodia-ironclad-friendship–1CE47UnGmt2/p.html

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View original content:https://www.prnewswire.co.uk/news-releases/cgtn-head-of-state-diplomacy-promotes-ironclad-friendship-between-china-and-cambodia-302432210.html

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