The Singapore Adult Glioma Therapeutics Market is valued at around $3 Mn in 2022 and is projected to reach $5 Mn by 2030, exhibiting a CAGR of 9.5% during the forecast period. The aging population, better diagnosis and healthcare infrastructure, and more awareness among some of the factors contributing to the industry's growth, which in turn is fueling demand for treatments and creating new avenues for the glioma therapeutics market to expand. Key players in the Singapore Adult Malignant Glioma Therapeutics Market include companies like Roche, Novartis, Merck & Co., Pfizer, Bristol-Myers Squibb, AbbVie, Cellagenics, ASTAR, Novogene, Oncohereos Pharma etc. among others.
The Singapore Adult Glioma Therapeutics Market is valued at around $3 Mn in 2022 and is projected to reach $5 Mn by 2030, exhibiting a CAGR of 9.5% during the forecast period.
A glioma is a kind of cancer that originates in the glial cells of the central nervous system, which includes the brain and spinal cord. Glial cells protect and sustain nerve cells; they are also the source of gliomas, which are tumours. Gliomas can be benign (non-cancerous) or malignant (cancerous). Macroglioblastoma Multiforme (GBM) is the most common kind of malignant glioma in adults. Gliomas are categorized using the World Health Organization's (WHO) grading system, which runs from grade I (least aggressive) to grade IV (most aggressive). The standard treatment for grade 2 gliomas is maximal resection plus single radiation therapy (RT), and for grade 3/4 malignant gliomas, it is maximal resection + RT + Temozolomide, albeit these regimens are still up for discussion.
With frequent advancements in therapeutic technologies, a considerable percentage of the population in Singapore is still impacted by adult malignant gliomas, which are especially common among older people. It mostly affects adults, with the 50s and 60s seeing the highest frequency. Given that Singapore's population is aging and will double by 2030, there will inevitably be more people in this age range who are vulnerable to gliomas. The aging population, better diagnosis and healthcare infrastructure, and more awareness are some of the factors contributing to the industry's growth, which in turn is fueling demand for treatments and creating new avenues for the glioma therapeutics market to expand.
Top participants in the global market, like Roche, which have well-known drugs like Temozolomide (Temodal), Avastin (Bevacizumab), and Novartis, which offers Glivec (Imatinib) for the treatment of certain forms of gliomas, also function in Signapore Market. Cellagenics, a Singapore-based local biotech firm has invested in research of personalised medication for treatment of Glioma.
Market Drivers
Advanced Infrastructure: Singapore's healthcare system operates well. Expert medical personnel and state-of-the-art medical facilities outfit the terrain for efficient glioma diagnosis and treatment. For patients undergoing therapy, this infrastructure acts as a reliable vessel that promotes early diagnosis, prompt action, and maybe safer conditions.
Therapeutic Innovation: Personalized medicine, immunotherapy, and targeted treatments are the next big things in the rapidly developing worldwide glioma therapeutics industry. Capable of driving these surges, Singapore enthusiastically accepts these new therapeutic possibilities. Increased insurance coverage and quicker regulatory approvals act as powerful currents that push these cutting-edge treatments into patient hands.
Increased Awareness: Gliomas and their treatment choices are made more widely known and understood through public awareness initiatives and patient advocacy organizations such as Brain Tumour Society Singapore. More information about dealing with conditions like gliomas is made available to the public through the Internet and media. Healthcare providers promote safer and better treatment options that can help the patient to recover faster.
Market Restraints
Market Size: Compared to healthcare superpowers like the US, Singapore's comparatively tiny population means that there is a smaller market for glioma treatments. This may impede investments in research and development by limiting the income potential for biotech startups and pharmaceutical businesses. Furthermore, even Singapore's strong healthcare system may be burdened by the high expense of treating gliomas, which includes surgery, radiation, and targeted medicines, restricting access for some patients.
Regulatory Hurdles: With patient safety as its priority, the Health Sciences Authority (HSA) upholds a strict regulatory framework for clinical trials and medication approvals. Although this methodical approach protects the public's health, it might prolong the process of developing and approving novel glioma treatments, which could postpone the availability of life-saving innovations.
High Competition: It's difficult to draw in and keep talented researchers and medical experts with glioma treatment expertise. Competition from nations with bigger research budgets and maybe greater pay puts Singapore at a competitive disadvantage, causing a brain drain and impeding the growth of a strong indigenous talent pool.
Singapore's Central Provident Funds (CPF) contributions and nationalized life insurance are two of the funding sources for the country's healthcare system. In addition to developing integrated, patient-centred techniques for the management of chronic diseases, Singapore is concentrating on value-based care and the exchange of best practices. The regulatory framework for therapeutic products in Singapore is overseen by the Health Sciences Authority (HSA).& New drug applications (NDAs) and generic drug applications (GDAs) are the two types of applications submitted in Singapore for the registration of medicinal products. Licenses to manufacture therapeutic items are awarded to companies that complete regulatory inspections and screening. The HSA oversees clinical trials, and medicinal products in Singapore need to be registered before they may be administered. It is a rigorous but effective system that manages patient safety and timely access to innovative treatments in an equitable manner.
Key Players
1. Executive Summary
1.1 Disease Overview
1.2 Global Scenario
1.3 Country Overview
1.4 Healthcare Scenario in Country
1.5 Patient Journey
1.6 Health Insurance Coverage in Country
1.7 Active Pharmaceutical Ingredient (API)
1.8 Recent Developments in the Country
2. Market Size and Forecasting
2.1 Epidemiology of Disease
2.2 Market Size (With Excel & Methodology)
2.3 Market Segmentation (Check all Segments in Segmentation Section)
3. Market Dynamics
3.1 Market Drivers
3.2 Market Restraints
4. Competitive Landscape
4.1 Major Market Share
4.2 Key Company Profile (Check all Companies in the Summary Section)
4.2.1 Company
4.2.1.1 Overview
4.2.1.2 Product Applications and Services
4.2.1.3 Recent Developments
4.2.1.4 Partnerships Ecosystem
4.2.1.5 Financials (Based on Availability)
5. Reimbursement Scenario
5.1 Reimbursement Regulation
5.2 Reimbursement Process for Diagnosis
5.3 Reimbursement Process for Treatment
6. Methodology and Scope
By Disease Type
By Treatment Type
By Distribution Channel
By Disease Stage
By Route of Administration
By End User
Methodology for Database Creation
Our database offers a comprehensive list of healthcare centers, meticulously curated to provide detailed information on a wide range of specialties and services. It includes top-tier hospitals, clinics, and diagnostic facilities across 30 countries and 24 specialties, ensuring users can find the healthcare services they need.
Additionally, we provide a comprehensive list of Key Opinion Leaders (KOLs) based on your requirements. Our curated list captures various crucial aspects of the KOLs, offering more than just general information. Whether you're looking to boost brand awareness, drive engagement, or launch a new product, our extensive list of KOLs ensures you have the right experts by your side. Covering 30 countries and 36 specialties, our database guarantees access to the best KOLs in the healthcare industry, supporting strategic decisions and enhancing your initiatives.
How Do We Get It?
Our database is created and maintained through a combination of secondary and primary research methodologies.
1. Secondary Research
With many years of experience in the healthcare field, we have our own rich proprietary data from various past projects. This historical data serves as the foundation for our database. Our continuous process of gathering data involves:
With extensive experience in the field, we have developed a proprietary GenAI-based technology that is uniquely tailored to our organization. This advanced technology enables us to scan a wide array of relevant information sources across the internet. Our data-gathering process includes:
2. Primary Research
To complement and validate our secondary data, we engage in primary research through local tie-ups and partnerships. This process involves:
Combining Secondary and Primary Research
By integrating both secondary and primary research methodologies, we ensure that our database is comprehensive, accurate, and up-to-date. The combined process involves:
Through this meticulous process, we create a final database tailored to each region and domain within the healthcare industry. This approach ensures that our clients receive reliable and relevant data, empowering them to make informed decisions and drive innovation in their respective fields.
We value your inquiry and offer free customization with every report to fulfil your exact research needs.