Fate Therapeutics Unveils New Clinical Findings at ACR Convergence 2025 Highlighting Immune Remodeling and Lasting Responses in Systemic Lupus Erythematosus Patients Treated with FT819 Off-the-Shelf CAR T-Cell Therapy
Clinical Trial Overview: Fate Therapeutics is conducting a Phase 1 clinical trial of FT819, an off-the-shelf CAR T-cell therapy, for patients with moderate-to-severe systemic lupus erythematosus (SLE), showing promising results with significant reductions in disease activity and favorable safety profiles.
Patient Outcomes: Among the first 10 patients treated, those surpassing the 3-month evaluation point demonstrated notable improvements in SLE Disease Activity Index scores, with some achieving complete renal response and sustained remission.
Safety and Administration: The treatment exhibited a favorable safety profile, with no dose-limiting toxicities and low-grade cytokine release syndrome, supporting the potential for same-day discharge after treatment, enhancing patient accessibility.
Future Directions: The company plans to expand its clinical program to include additional autoimmune diseases and is working with the FDA to design a registrational study, aiming to initiate a pivotal study in 2026.
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- Massive Market Potential: The global next-gen treatment market is projected to reach $88.85 billion by 2030, driven by a surge in funding for high-tech cures, positioning Avant Technologies at the center of this transformation with significant market opportunities.
- Technological Innovation: Avant's cell encapsulation technology addresses the immune rejection issue in regenerative medicine, allowing genetically modified cells to thrive in the body long-term, significantly reducing the side effects of traditional treatments and enhancing patient quality of life.
- Strategic Partnerships: The collaboration with SGAustria to develop diabetes treatments targets a market projected to reach 853 million patients by 2050, positioning Avant's technology to capture a significant share of this vast market.
- Diversified Market Approach: Avant's second joint venture, Klothonova, focuses on anti-aging and age-related diseases, backed by over 50 peer-reviewed studies, showcasing its strategic advantage across multiple high-value healthcare markets.
- Massive Market Potential: The global next-gen treatment market is projected to reach $88.85 billion by 2030, driven by a surge in funding for high-tech cures, positioning Avant Technologies at the center of this transformation with significant market opportunities.
- Technological Breakthrough: Avant's cell encapsulation technology addresses a fundamental issue in regenerative medicine by protecting therapeutic cells from immune system attacks, significantly reducing the side effects associated with traditional drugs and enhancing treatment efficacy.
- Strategic Partnership: The collaboration with SGAustria aims to develop treatments for diabetes using genetically modified cells that produce insulin, potentially offering new therapeutic options for the 589 million diabetes patients worldwide, highlighting substantial market potential.
- Diverse Market Applications: Avant's technology is not limited to diabetes but can also be applied to Alzheimer's and cardiovascular diseases, with related markets expected to reach $32.8 billion by 2033, showcasing strong market adaptability and growth potential.

- Massive Market Potential: The global next-gen treatment market is projected to reach $88.85 billion by 2030, driven by a surge in funding for high-tech cures, positioning Avant Technologies and others at the forefront of this transformation with significant market opportunities.
- Technological Innovation: Avant Technologies' cell encapsulation technology protects genetically modified cells in the body, addressing the side effects of traditional drugs, which is expected to dramatically improve the quality of life for diabetes patients and tap into a substantial market potential.
- Strengthened Partnerships: Avant's collaboration with SGAustria aims to develop a bio artificial pancreas, potentially offering innovative treatment solutions for the 589 million diabetes patients worldwide, addressing the growing market demand.
- Diversified Market Strategy: Avant's second venture, Klothonova, targets age-related diseases using the therapeutic potential of Klotho protein, which is expected to penetrate multiple high-value healthcare markets, further enhancing the company's strategic positioning.

- Massive Market Potential: The global next-gen treatment market is projected to reach $88.85 billion by 2030, driven by a surge in funding for high-tech cures, positioning Avant Technologies at the center of this transformation with significant competitive advantages.
- Technological Breakthrough: Avant's cell encapsulation technology protects therapeutic cells from immune system attacks, enabling safer treatments for diabetes patients and is expected to dramatically improve their quality of life.
- Strategic Partnerships: Avant's collaboration with SGAustria aims to develop a bio artificial pancreas for the 589 million people living with diabetes globally, with projections indicating this number could rise to 853 million by 2050, highlighting substantial market opportunities.
- Diverse Market Expansion: Avant's second venture, Klothonova, focuses on anti-aging therapies using Klotho protein, targeting multiple high-value markets such as Alzheimer's and cardiovascular diseases, showcasing the versatility and strategic advantage of its core technology.
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Clinical Trial Overview: Fate Therapeutics is conducting a Phase 1 clinical trial of FT819, an off-the-shelf CAR T-cell therapy, for patients with moderate-to-severe systemic lupus erythematosus (SLE), showing promising results with significant reductions in disease activity and favorable safety profiles.
Patient Outcomes: Among the first 10 patients treated, those surpassing the 3-month evaluation point demonstrated notable improvements in SLE Disease Activity Index scores, with some achieving complete renal response and sustained remission.
Safety and Administration: The treatment exhibited a favorable safety profile, with no dose-limiting toxicities and low-grade cytokine release syndrome, supporting the potential for same-day discharge after treatment, enhancing patient accessibility.
Future Directions: The company plans to expand its clinical program to include additional autoimmune diseases and is working with the FDA to design a registrational study, aiming to initiate a pivotal study in 2026.







