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57 company, guide, and curated content matches · plus news and online publication results
…RNA delivery carrier for in vivo CAR T generation 兼具T细胞激活作用的mRNA载体用于体内CAR-T生成 2026-08-12 Nature Materials Qiannan Cao; Yingli Yao; Wenming Zheng; Hongqian Liu; Mingxia Jiang; Dayang Xie; Siting Zhang; Pijun Su; Huilin Yuan; Xiaoyuan Chen; Huapan Fang; Huayu Tian in-vivo-engineering Research The auth…
In Vivo Cell Engineering & Gene Editing
…哪些分布与安全性测量？ 动物模型结果向人体转化时有哪些证据缺口？ 递送、表达、编辑与疗效不是同一终点；明确区分细胞、动物与人体证据。 In Vivo Cell Engineering & Gene Editing Explore in vivo CAR-T, nonviral editing delivery, cell targeting, and relevant measurement methods. How do delivery, expression, functional editing, and therapeutic activity differ? Which distr…
In Vivo Cell Engineering & Gene Editing
…d clinical dosing. AVO-103 is a TCR program and is kept separate from CAR-T. AAVivo lists CD19 AVO-100, BCMA AVO-101, and dual BCMA/CD19 AVO-102 using T-cell-targeted AAV. The disclosed activities include vector production and construct optimization, not verified clinical dosing. AVO-103 is a TCR pr…
In Vivo Cell Engineering & Gene Editing
…ner uBriGene identifies Cellinfinity’s CIB-301 and CIB-350 as in vivo CAR-T programs for hematologic and solid tumors, supported by lentiviral vector manufacturing. The March 2026 announcement does not establish a registered clinical phase or human efficacy. Manufacturing partner uBriGene identifies…
In Vivo Cell Engineering & Gene Editing
CREATE, formerly Myeloid Therapeutics, disclosed preclinical in vivo CAR-T/CAR-NK and all-RNA RetroT work at AACR 2026. Clinical MT-302 is a myeloid-cell program, not evidence that its CAR-T programs have reached the same stage. The former name is retained as an alias. CREATE, formerly Myeloid Thera…
In Vivo Cell Engineering & Gene Editing
…IND preparation. EVM14 and EVM16 are cancer vaccines, not its in vivo CAR-T lead. EVM18 delivers CD19 CAR mRNA in targeted LNPs. Everest’s 2026 interim results report IIT initiation in autoimmune disease and global IND preparation. EVM14 and EVM16 are cancer vaccines, not its in vivo CAR-T lead. Cor…
In Vivo Cell Engineering & Gene Editing
GenVivo identifies GEN-310 as an in vivo CAR-T/NK program for B-cell malignancies. Its October 2025 corporate presentation classifies GEN-310 as preclinical. Clinical work on separate immunocytokine vectors should not be used to upgrade this CAR program. GenVivo identifies GEN-310 as an in vivo CAR-…
In Vivo Cell Engineering & Gene Editing
… engineering field; it should not be labeled as equivalent to in vivo CAR-T. Intellia presents CRISPR gene-editing science, clinical programs, and scientific publications on its official website. Its gene-editing work belongs in this broader in vivo engineering field; it should not be labeled as equ…
In Vivo Cell Engineering & Gene Editing
Sail combines eRNA with targeted nanoparticles for in vivo CAR-T in immune-mediated diseases. Its July 2026 Johnson & Johnson collaboration includes an option to acquire Sail, not a completed acquisition. A named clinical CAR-T candidate is not established by this announcement. Sail combines eRNA wi…
In Vivo Cell Engineering & Gene Editing
…odifying T or NK cells in vivo. It is kept separate from gene-encoded CAR-T because protein-based receptor installation has a different mechanism. The website does not establish human efficacy. Singular’s iCAR is a recombinant fusion-protein approach to modifying T or NK cells in vivo. It is kept se…
In Vivo Cell Engineering & Gene Editing
…ecombinases with cell-targeted LNP delivery to create durable in vivo CAR-T through sequence-specific insertion. Its platform disclosure establishes preclinical research intent and mechanism, not patient benefit or demonstrated clinical safety. Stylus combines engineered recombinases with cell-targe…
In Vivo Cell Engineering & Gene Editing
Aanastra discloses PEP-CAR, an anti-CD19 in vivo CAR-T strategy combining engineered RNA and targeting peptides for cancer and autoimmune disease. The public website does not establish a registered clinical program or validated patient outcomes. Aanastra discloses PEP-CAR, an anti-CD19 in vivo CAR-T…
In Vivo Cell Engineering & Gene Editing
Umoja announced four accepted ASH presentations, including clinical data from investigator-initiated studies of CD22-directed UB-VV400 in B-cell malignancies and UB-VV410 in lupus. Separate trial-in-progress posters concern UB-VV400 and BCMA/GPRC5D-directed UB-VV500. The announcement schedules December presentations rather than providing numerical response or safety results from those studies.
Tessera announced three preclinical presentations for the December 2026 ASH meeting. Topics include targeted LNP delivery for functional CAR-T generation in nonhuman primates and in vivo hematopoietic stem-cell editing for sickle cell disease. This is a company announcement of upcoming presentations, not a peer-reviewed publication or evidence of clinical benefit.
Tempest outlined TPST-4003, an in vivo CAR-T candidate using CD7-targeted mRNA/LNP delivery of a dual CD19/BCMA CAR. A planned investigator-initiated study would enroll approximately ten patients with nervous-system autoimmune diseases, initially including myasthenia gravis and multiple sclerosis, with dosing anticipated in the fourth quarter. This is a development plan, not human efficacy evidence for the in vivo candidate.
Screening eight ionizable lipids identified a lead formulation that delivered reporter RNA to several immune-cell types. Researchers then used it to engineer primary human T cells expressing a MUC1-directed CAR, with cytotoxic activity against antigen-positive tumor cells in vitro. Animal reporter experiments supported delivery feasibility, but the study does not demonstrate therapeutic CAR-T generation inside patients or animals.
Typewriter Therapeutics emerged from stealth with $56 million in Series A financing led by AN Venture Partners and RA Capital. Its platform uses LNP-delivered RNA, including mRNA encoding an R2 protein, to pursue targeted insertion of therapeutic genes. Initial priorities include in vivo CAR T and genetic liver disease. The funding announcement does not establish human safety, durability, or clinical benefit.
A polymer-lipid carrier incorporating arginine-modified oligoethylenimine combined T-cell activation with mRNA delivery without an added targeting ligand. The formulation favored splenic delivery and engaged PI3K-AKT-mTOR signaling. FAP-CAR mRNA generated functional CAR T cells in experimental cancer and fibrosis settings. These are preclinical results; the article also has a subsequent publisher correction that should accompany interpretation.
