
11 - 12 March 2026 | Sands Expo and Convention Center, Singapore
Drug Product Mapping in Southeast Asia Clinical Trials
Introduction
Southeast Asia has become an increasingly important hub for clinical trials, driven by its diverse patient populations, competitive costs, and rapidly improving healthcare infrastructure. Countries like Singapore, Thailand, Malaysia, Indonesia, Philippines and Vietnam have emerged as attractive destinations for both regional and global clinical research.
This eBook, Drug Product Mapping in Southeast Asia, provides a comprehensive overview of the clinical trial landscape in the region, highlighting key trends, regulatory advancements, and the types of drug products being developed. It includes detailed country-specific insights and a mapping of companies and their drug product pipelines, ranging from cell and gene therapies to antibody-drug conjugates (ADCs), vaccines, and beyond.
Whether you're a biopharma company exploring opportunities in Southeast Asia or a stakeholder interested in the region's clinical trial ecosystem, this eBook serves as a valuable guide to understanding the region's growing potential and strategic significance in global drug development.

Diverse Population
Broader exploration of diverse demographic
The region’s unique demographic mix allows researchers to study a wide range of genetic variations and diseases, making it an ideal setting for clinical trials, particularly in oncology, infectious diseases, and rare genetic disorders.

Cost-Effectiveness
Lower trial costs compared to Western markets.
Southeast Asia offers significant cost advantages compared to traditional clinical trial markets in Europe and North America. The availability of skilled clinical trial professionals, coupled with lower labor and operational costs, makes the region an appealing option for biopharma companies looking to streamline trial expenses without compromising on quality.

Infrastructure Investments
Expansion of clinical trial networks and advanced facilities.
The region's growing prominence is also supported by increasing investments in healthcare technology, data analytics, and clinical trial management systems. These advancements are improving trial efficiency and patient recruitment while ensuring better data integrity and compliance with international standards.
Current Landscape of Biopharma in Southeast Asia

Regional R&D hub with strong infrastructure.
In 2023, Singapore approved 138 clinical trials, showcasing its position as a key hub in the Asia-Pacific region. With a strong focus on innovation, world-class research infrastructure, and efficient regulatory pathways, the country continues to attract global sponsors across diverse therapeutic areas, particularly in oncology and precision medicine.
Lilly Digital Health and the Lilly Centre for Clinical Pharmacology (LCCP), a subsidiary of Eli Lilly and Company, have launched a SGD$42 million Digital Health Innovation Hub in Singapore. The hub aims to accelerate the development of AI-powered digital health technologies, enhancing patient insights outside the clinic. It will support Eli Lilly's global clinical teams across key therapeutic areas, including cardiometabolic health, neurodegeneration, pain, oncology, and immunology.

Government initiatives promoting clinical trials.
Thailand is rapidly emerging as a key player in the global clinical trial landscape, with the market expected to reach USD 3.5 billion by 2027. The country’s strategic location in Southeast Asia provides access to a diverse patient population, essential for robust clinical research. As of the latest available data, Thailand has conducted a significant number of clinical trials, with the country hosting over 1,200 clinical trials registered on ClinicalTrials.gov, with a steady increase in new trials being initiated each year. The country aims to enhance health equity through universal coverage and bolster Thai health technology and innovation. Thailand is also concentrating on developing high-quality products, particularly in advancing oncology treatments and biotechnology.
For the first time ever, a cross-national DCT has been planned, involving patients from Thailand participating online. NCC and designated Thai partner institutions will conduct a cross-border DCT as a demonstration project in collaboration with pharmaceutical companies. The aim of this project is to streamline procedures on DCTs between the two countries and explore methods that will allow for more international clinical trials to be conducted in a simple, fast, and cost-effective manner.

Malaysia is gaining momentum as a clinical trial hub, with 276 sponsored clinical studies recorded—a 24% year-on-year increase. Notably, Phase II and III trials dominate the landscape, reflecting a growing focus on late-stage drug development. This growth is fueled by efficient regulatory frameworks, a centralized ethics approval system, and strong government support, making Malaysia a cost-effective destination with a diverse patient population and expanding focus on oncology and metabolic disorders.
AstraZeneca invested RM5.5 billion research and development facility is equipped with cutting-edge robotics, high-throughput screening, and Al-driven technology, forging partnership with Ministry of Health.

Between January 2018 and November 2023, clinical trials in Indonesia—both multi-country and single-country—have been distributed across all phases, with a significant focus on later-phase trials, particularly Phase IV.
In July of 2023, the MOH signed a decree establishing the national Indonesia Clinical Research Center (INA-CRC). Its function is to coordinate and facilitate clinical trial across all hospitals. The purpose of this requirement is to ensure that hospitals are adequately prepared to serve as sites for clinical trials.

The Philippines is steadily emerging as a regional player in clinical research. Supported by efficient ethics approval systems and government initiatives such as the establishment of “Pharma Ecozones,” the country aims to enhance R&D, local drug manufacturing, and innovation capacity. Key therapeutic areas include oncology, infectious diseases, and metabolic disorders, with trials increasingly focused on late-stage development. While local drug discovery remains limited, the government’s pharma roadmap targets stronger self-sufficiency and local innovation by 2030.
AstraZeneca’s planned PHP 7 billion investment to build an Oncology Innovation Center underscores growing confidence in the country’s biopharma ecosystem.
In early 2025, AstraZeneca announced plans to expand its clinical trial activities in the Philippines. The initiative aims to strengthen local research capabilities, retain healthcare professionals, and enhance patient access to cutting-edge therapies and innovative medicines.

Vietnam is rapidly positioning itself as a hub for biologics and vaccine production in Southeast Asia, fueled by strong foreign partnerships and technology transfer agreements. Sanofi and VNVC recently launched a vaccine manufacturing facility in Long An, expected to produce up to 100 million doses annually, while VNVC’s collaboration with Russia’s Medsintez will enable local production of biologics such as insulin, recombinant albumin, and semaglutide. With increasing participation in global studies and a supportive government framework, Vietnam continues to strengthen its presence in the regional biopharma and clinical trials landscape.
The country has hosted several notable trials, including the Phase 2A study of the cancer immunotherapy drug RBS2418 and the local registration of GC Biopharma’s varicella vaccine, BARYCELA.
Ho Chi Minh City Oncology Hospital announced active 37 international clinical trials, the majority of which are Phase 3 studies.
Drug Product Mapping in Southeast Asia


Conclusion
Southeast Asia is cementing its position as a pivotal region in the global clinical trial landscape. With advancements in regulatory pathways, diverse patient demographics, and increasing experience across trial phases, countries like Singapore, Malaysia, Indonesia, and others are becoming go-to destinations for biopharma innovation. From cell and gene therapies to antibody-drug conjugates and vaccines, the region's drug product pipeline reflects its dynamic growth and potential to shape the future of clinical research.
As the Southeast Asian clinical trial ecosystem evolves, staying informed and connected is crucial. To delve deeper into these trends, network with key players, and explore the latest innovations, join us at The 3rd Annual Clinical Trials Festival Asia 2025. Taking place on 12-13 March 2025, this premier event will bring together industry leaders, regulators, and researchers to discuss the future of clinical trials in the Asia-Pacific region.
Join Biologics Manufacturing Asia 2026!

Asia’s Foremost Clinical Trials Conference Uniting Clinical Trials Leaders
11 - 12 March 2026 | Sands Expo & Convention Centre, Singapore
Attendees
Companies
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Contact

Umairoh Nurul Hafifa, Conference Producer
[email protected] +62 856 0026 7725

Ana Laxamana, Regional Business Development Lead
[email protected] +65 6983 6132

