The Brazil cell and gene therapy market size reached USD 298.30 Million in 2025. The market is projected to reach USD 794.01 Million by 2034, exhibiting a growth rate (CAGR) of 11.49% during 2026-2034. Strategic alliances, increased funding for rare disease research, and the creation of national research institutions are driving the cell and gene therapy market. These efforts enhance local production, strengthen research capacity, promote technology transfer, ensure equitable access, thereby contributing to the expansion of the Brazil cell and gene therapy market share.
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Report Attribute
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Key Statistics
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Base Year
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2025
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Forecast Years
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2026-2034
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Historical Years
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2020-2025
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| Market Size in 2025 | USD 298.30 Million |
| Market Forecast in 2034 | USD 794.01 Million |
| Market Growth Rate 2026-2034 | 11.49% |
Strategic Collaborations Enhancing Access to Advanced Therapies
Collaborative partnerships among global biotech leaders, research organizations, and healthcare providers are greatly advancing the Brazil’s cell and gene therapy sector. These partnerships facilitate the exchange of technical knowledge, enhance clinical research capabilities, and create a dependable framework for the development of large-scale therapies. Collaborations with international organizations enable a transfer of knowledge, permitting Brazilian institutions to embrace advanced technologies in manufacturing, quality control, and clinical implementation. These efforts additionally improve the access to cutting-edge treatment options for patients, closing the divide between innovation and availability. The resulting ecosystem encourages workforce growth via targeted training initiatives and supports compliance with international regulatory and safety standards. Furthermore, global collaboration enhances clinical execution by linking local research networks with international therapeutic pathways, resulting in quicker approval and market launch schedules. These joint initiatives collectively broaden the scope of precision medicine and establish Brazil as a regional frontrunner in innovations related to cellular and genetic treatments. In line with this trend, in 2025, CTMC (Resilience & MD Anderson Cancer Center) partnered with Einstein Hospital Israelita in Brazil to launch the Global Cell Therapy Network Alliance, aiming to expand cell therapy access in Brazil and Latin America. The collaboration focuses on accelerating adoption and clinical implementation of advanced cellular therapies across the region.
Strengthened Investment in Rare Disease Research and Local Manufacturing
The increase in funding for rare disease research, along with programs supporting domestic production, is a significant factor impelling the Brazil cell and gene therapy market growth. Monetary support from international and local partners facilitates the creation of strong research and development (R&D) pipelines focused on creating therapies for diseases with few treatment alternatives. Through significant investment in clinical trials, infrastructure, and workforce education, these programs promote the development of sophisticated therapeutic platforms suited to Brazil's healthcare requirements. Technology transfer agreements also bolster local capabilities, facilitating domestic production that diminishes reliance on imported treatments and lowers costs. Incorporating these innovations into the public health system guarantees that advanced therapies reach a broader population segment. This convergence of scientific investment, local skill development, and fair healthcare access not only support market growth but also bolsters Brazil's status as a prominent biotechnology center in Latin America. Directly illustrating the significant investment in R&D and local production, GEMMABio partnered with Fiocruz in 2024 to fund and develop gene therapy treatments for rare diseases in Brazil with up to $100 million supporting research, clinical trials, and local manufacturing. The collaboration included technology transfer to enable local production and broader access through Brazil’s public health system (SUS). Initial programs targeted GM1 gangliosidosis, Krabbe Disease, Metachromatic leukodystrophy, and three additional therapies, aiming to make advanced treatments affordable nationwide.
Establishment of National Research Institutions Promoting Innovation
The establishment of specialized national institutes focused on cell and gene therapy research is fueling considerable progress in Brazil’s biotechnology industry by uniting scientific expertise, clinical capacity, and technological resources to accelerate the development and translation of advanced genetic treatments. Centralized organizations offer an organized system for teamwork among academic researchers, clinicians, and industry experts, guaranteeing effective alignment of scientific and clinical initiatives. By uniting knowledge and resources, these centers expedite the exploration, verification, and application of gene-based therapies into effective medical solutions. They further enhance the nation's innovation ecosystem by backing advanced training initiatives and developing a skilled workforce adept at managing intricate genetic technologies. Moreover, these institutions act as national reference centers for regulatory alignment, ethical supervision, and quality assurance, encouraging compliance with international standards. Their emphasis on precision medicine fosters the creation of targeted treatments for cancer and various genetic disorders, establishing Brazil as a leader in regional progress within genomic science. For instance, in 2025, Brazilian research groups launched the National Institute of Gene Therapy (C2PO) to advance gene therapy research and applications. The institute aims to centralize efforts in precision oncology and foster collaboration among scientists, laboratories, and clinicians.It will focus on research, training, and education to accelerate the development of innovative gene-based treatments in Brazil.
IMARC Group provides an analysis of the key trends in each segment of the market, along with forecasts at the country and regional levels for 2026-2034. Our report has categorized the market based on therapy type, indication, delivery mode, and end user.
Therapy Type Insights:
The report has provided a detailed breakup and analysis of the market based on the therapy type. This includes cell therapy (stem cell (pluripotent stem cell, cancer stem cell, and adult stem cell) and non-stem cell (T-cell, natural killer cell, and others)) and gene therapy.
Indication Insights:
A detailed breakup and analysis of the market based on the indication have also been provided in the report. This includes cardiovascular disease, oncology disorder, genetic disorder, infectious disease, neurological disorder, and others.
Delivery Mode Insights:
The report has provided a detailed breakup and analysis of the market based on the delivery mode. This includes in-vivo and ex-vivo.
End User Insights:
A detailed breakup and analysis of the market based on the end user have also been provided in the report. This includes hospitals, cancer care centers, pharmaceuticals and biotechnology companies, and others.
Regional Insights:
The report has also provided a comprehensive analysis of all the major regional markets, which include Southeast, South, Northeast, North, and Central-West.
The market research report has also provided a comprehensive analysis of the competitive landscape. Competitive analysis such as market structure, key player positioning, top winning strategies, competitive dashboard, and company evaluation quadrant has been covered in the report. Also, detailed profiles of all major companies have been provided.
| Report Features | Details |
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| Base Year of the Analysis | 2025 |
| Historical Period | 2020-2025 |
| Forecast Period | 2026-2034 |
| Units | Million USD |
| Scope of the Report |
Exploration of Historical Trends and Market Outlook, Industry Catalysts and Challenges, Segment-Wise Historical and Future Market Assessment:
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| Therapy Types Covered |
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| Indications Covered | Cardiovascular Disease, Oncology Disorder, Genetic Disorder, Infectious Disease, Neurological Disorder, Others |
| Delivery Modes Covered | In-vivo, Ex-vivo |
| End Users Covered | Hospitals, Cancer Care Centers, Pharmaceuticals and Biotechnology Companies, Others |
| Regions Covered | Southeast, South, Northeast, North, Central-West |
| Customization Scope | 10% Free Customization |
| Post-Sale Analyst Support | 10-12 Weeks |
| Delivery Format | PDF and Excel through Email (We can also provide the editable version of the report in PPT/Word format on special request) |
Key Questions Answered in This Report:
Key Benefits for Stakeholders: