September 2024
The global cell therapy market size was estimated at US$ 4.79 billion in 2023 and is projected to grow to US$ 44.39 billion by 2034, rising at a compound annual growth rate (CAGR) of 22.69% from 2024 to 2034. The focus on developing therapeutics for rare diseases is driving the market growth.
Unlock Infinite Advantages: Subscribe to Annual Membership
The delivery of chosen, modified, or changed cells outside of the body for the purpose of treating or preventing illness is known as cell therapy. With intriguing and developing potential for therapeutic use, cell therapy is a field on the rise. The manufacturing and culturing procedures must develop before these medicines may be used commercially, which usually entails drastically scaling up and automating to match the clinical demand. Over the past twenty years, research at government and university institutions throughout the globe has substantially advanced our knowledge of cell treatments. Different cell types will be researched for possible uses and developed into treatments as innovative cell therapies while the study is still in its early stages.
There are benefits and drawbacks to using AI in cell therapy. AI technology integration may save costs, streamline logistics, and increase production accuracy and efficiency. AI may also be used to forecast treatment outcomes, track the course of therapy, and identify people who would benefit from it. Furthermore, work is still to be done on the validation of AI-based judgments and the integration of AI systems into current production workflows.
For instance,
| Company Name | 2seventy Bio, Inc. |
| Headquarters | Massachusetts, U.S., North America |
| Recent Development | In April 2024, Regeneron Pharmaceuticals, Inc. completed the asset purchase agreement ("APA"), according to 2seventy Bio, Inc. As part of their recently created cell therapies business, Regeneron employed over 160 workers from 2seventy Bio and acquired all of their research and development initiatives related to autoimmune and cancer under the provisions of the American Psychological Association. Moving ahead, 2seventy Bio will work in tandem with their partner Bristol Myers Squibb (BMS) to exclusively concentrate on the marketing and development of Abecma (idecabtagene vicleucel), their BCMA-targeted CAR T cell treatment for multiple myeloma. |
| Company Name | Astellas Pharma Inc. |
| Headquarters | Tokyo, Japan, North America |
| Recent Development | In May 2024, to create unique convertibleCAR® projects by merging the state-of-the-art cell therapy platforms from both businesses, Astellas Pharma Inc. and Poseida Therapeutics, Inc. have formed a research partnership and licensing agreement. Poseida and Xyphos Biosciences, Inc., a fully owned subsidiary of Astellas, or "Xyphos," have established this arrangement. |
Adult bone marrow stem cells produce a variety of growth factors that enable them to differentiate into the kind of cells required for heart and blood vessel repair. With the use of stem cells, it is possible to stimulate the production of new, healthy skin tissue, boost collagen synthesis, hasten the growth of hair after haircuts or hair loss, and replace damaged or scarred tissue with freshly produced, healthy tissue. Adult stem cells injected into the brain can help regenerate new brain synapses, neurons, and cells after brain damage or cognitive impairment in illnesses such as Parkinson's and Huntington's. The use of stem cells in treating severe and debilitating autoimmune illnesses gives new hope. This therapy may be beneficial for patients with pain related to spinal diseases, orthopedic concerns, and sports injuries.
Cellular and gene therapy are two of the priciest therapies currently offered. Cell treatments are expensive, usually costing more than $400,000 USD and often more than $1 million USD per patient, and there are technological issues that raise questions about their accessibility and affordability for patients, payers, and healthcare systems both domestically and abroad. Budgets for healthcare may also be strained by the expense of cell treatment, forcing governments and insurance companies to make tough decisions about how best to distribute funds and cover different products. The costs involved in producing and administering cell therapy are one factor contributing to its high cost. Specialized equipment, trained personnel, and strict quality control systems could be required for each of these processes.
One of the newest and most promising treatments for blood cancer is CAR-T cell therapy. Through the activation of the immune system, these medicines support the fight against cancer. Future cancer treatments might greatly benefit from CAR T-cell therapy because of its many advantages. CAR T cells have proven to be a successful treatment for several cancers, particularly blood cancers like leukemia and lymphoma. The specific antigen that is present in malignant cells is the target of CAR T cells. This modification reduces harmful effects and harm to healthy tissues to a minimum. The purpose of CAR T cells is to multiply and persist throughout the body. This suggests that they could offer long-term protection against the cancer coming back.
For instance,
By therapy type, the autologous therapy segment dominated the cell therapy market in 2023. Autologous cell therapy, with applications in immuno-oncology and regenerative medicine, is a fast-expanding therapeutic method. Autologous methods have the important benefit of reducing the danger of immunological rejection in patients and fostering long-term recovery. The ability to tailor autologous cell treatment to the specific requirements of each patient is an additional advantage. Thus far, this type of treatment has shown effective in treating burns and pressure ulcers, promoting wound healing, reducing chronic inflammation, and improving postoperative healing—all while bioengineering skin replacements.
For instance,
By therapeutic area, the oncology segment held the largest share of the cell therapy market in 2023. Cell therapy is essential to our goal of making cancer no longer a leading cause of death due to the disease's rising incidence. In cell-mediated immunity and T-cell genetic modification techniques, T-cells are crucial. Therapeutic promise for preventing tumor formation has been demonstrated by CAR-T cell and TCR-T cell treatments, which have shown promising clinical outcomes in clinical studies.
For instance,
In May 2024, Elicera Therapeutics is about to begin CARMA, its first clinical CAR T-cell research, with the goal of gathering vital information for both the immune-boosting iTANK technology and its flagship CAR T-cell candidate, ELC-301. The purpose of the two-part CARMA phase I/IIa trial is to evaluate the safety and effectiveness of ELC-301 in patients with advanced malignancies associated with B cells.
By region, North America dominated the cell therapy market share by 59% in 2023. North America is considered technologically advanced, with advanced healthcare infrastructure and research centers equipped with advanced systems. With time, the region has focused on providing better therapeutics and medicines to treat illness with the help of key organizations and governments. These factors have significantly contributed to the growth of the market in this region. The major countries that have contributed to this growth are the U.S. and Canada.
The U.S. holds the largest share of the cell therapy market in North America, and one of the main reasons for that is the growing prevalence of cancer. The U.S. is among the top countries with a large number of cancer cases. Cell therapy has proven to be highly useful in conducting cancer research and cancer therapeutics. With the growing number of cancer cases, the country is heavily focused on cancer research.
In order to guarantee that Canada stays at the forefront of innovation and research into new technologies, the government of Canada is committed to investing in these areas. The Strategic Science Fund provides up to $171.6 million in support for independent scientific and research institutions, as announced by the Minister of Health. As announced in December 2023, the money will assist five groups in Ottawa and was granted following a new open, merit-based, competitive procedure that was guided by the recommendations of an impartial expert review panel.
By region, Asia Pacific is expected to grow at a significant rate during the forecast period. Asia Pacific’s cell therapy market is growing due to multiple factors. One of the major factors is government initiatives. The governments of China, India, and Japan are majorly contributing to the market. To this date, various cell therapies have been approved in the Asia Pacific, which are listed in the table, and more research is going on to develop new cell therapies.
For instance,
| CAR-T Cell Therapies Approved in Asia | |||
| Brand | Manufacturer | Country | Year of Approval |
| Carvykti | Legend Biotech, J&J | Japan & South Korea | 2023 |
| Yuanruida (CNCT19) | JUVENTAS | China | 2023 |
| Carteyva | JW Therapeutics | China | 2021 |
| Fucaso | IASO BIO, Innovent | China | 2023 |
| Saikaize (Zevor-cel) | Carsgen Therapeutics | China | 2024 |
| Abecma | BMS, bluebird bio | Japan | 2022 |
| Breyanzi | BMS | Japan | 2021 |
| Yescarta | Kite Pharma, Fosun Kite | Japan & China | 2021 |
| Kymriah | Novartis | Japan, South Korea and Taiwan | 2021 |
India is becoming a hub of cancer due to smoking, environmental factors, and consumption of carcinogens. The lack of treatment options is leading to numerous cancer-related deaths. To Mitigate this, the Indian Government has taken various initiatives to utilize cell therapies for the treatment of cancer.
For instance,
| Cell and Gene Therapy R&D Projects Supported by Indian DBT from 2020-2024 | |
| Output | Number |
| Scientists Supported | 228 |
| Projects Supported | 144 |
| Manpower Supported | 307 |
| Publications | 105 |
| Patents Filed/Granted | 7 |
| Technologies/Products Developed | 6 |
| Workshop/Training Programs Organized | 5 |
By Therapy Type
By Therapeutic Area
By Region
September 2024
September 2024
September 2024
September 2024
Deepa has certified the degree of Master’s in Pharmacy in the Pharmaceutical Quality Assurance department from Dr D.Y. Patil College of Pharmacy. Her research is focused on the healthcare industry. She is the author or co-author of four Review Articles, which include Solid dispersion a strategic method for poorly soluble drugs and solubility improvement techniques for poorly soluble drugs, Herbal Drugs Used In Treatment Of Cataracts, Nano sponges And Their Application in Cancer Prevention and Ayurvedic Remedies of Peptic ulcer. She has also published a Research Article on the Formulation and Evaluation of Mucoadhesive Tablets of Miconazole cocrystal which was published in GIS Science Journal Volume 9 Issue 8. Her passion for secondary research and desire to take on the challenge of solving unresolved issues is making her flourish is the in the research sector.