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BioWorld - Monday, December 22, 2025
Home » Topics » Cell therapy, BioWorld Science

Cell therapy, BioWorld Science
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KRAS protein
Immuno-oncology

Medigene selects lead candidate for MDG-2021 program

June 21, 2024
Medigene AG has selected its lead candidate for MDG-2021, a T-cell receptor engineered T-cell (TCR-T) therapy targeting KRAS G12D with human leukocyte antigen (HLA)-A*11 being developed in combination with the company’s PD1-41BB costimulatory switch protein (CSP) technology.
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Immuno-oncology

Yellowstone Biosciences launches with focus on bispecific TCR-based therapies for cancer

June 20, 2024
Yellowstone Biosciences Ltd. has launched with a focus on soluble bispecific T-cell receptor (TCR)-based therapies for human leukocyte antigen (HLA) class II (HLA-II) targets in oncology.
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Red blood cells on blue background
Hematologic

Be Biopharma’s BE-101 awarded US orphan drug designation for hemophilia B

June 5, 2024
The FDA has granted orphan drug designation to Be Biopharma Inc.’s BE-101, a novel engineered B-cell medicine being developed for the treatment of hemophilia B.
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Leukemia illustration
Immuno-oncology

Bluesphere’s TCR cell therapy BSB-1001 receives IND clearance for leukemia

June 4, 2024
Bluesphere Bio Inc. has received FDA clearance of its IND application for BSB-1001 for patients with relapsed or refractory acute myeloid leukemia (AML), acute lymphocytic leukemia and myelodysplastic syndromes, in conjunction with allogeneic hematopoietic stem cell transplantation (alloHSCT).
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Induced pluripotent stem cells
Ocular

Series A readies Rxcell's iPSC-derived photoreceptors for clinic

April 16, 2024
By Tamra Sami
On the heels of a $4.6 million series A round in December 2023, cell therapy company Rxcell Inc. is planning to raise another $15 million in 2024 to take its iPSC-derived photoreceptors to the clinic for retinitis pigmentosa and other degenerative diseases of the retina.
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T cells attacking cancer cells
Cancer

With $150M in hand, Clasp launches with T-cell engagers

March 26, 2024
By Lee Landenberger
One of the building blocks for newly launched Clasp Therapeutics Corp. is making the right patient choices for treatment. If those who receive the company’s therapy are correctly identified, CEO Robert Ross told BioWorld, it will have a profound effect on outcomes. The missing link in cancer treatment, Ross added, was how to identify a patient, something he said Clasp is able to do.
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Dendritic cells
Cancer

Asgard’s ‘direct reprogramming strategy’ garners €30M series A

March 18, 2024
By Nuala Moran
Asgard Therapeutics AB has raised €30 million (US$32.8 million) in a series A round to advance a novel approach to cancer immunotherapy, in which it is proposed to reprogram cancer cells into functional antigen-presenting dendritic cells in vivo, activating a host immune response against the tumor.
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Co-culture that shows the CAR T-cell clusters attacking the tumor cells (in green)
Immuno-oncology

TYRP1 CAR T-cell therapy shows activity in models of melanoma

Feb. 22, 2024
Researchers from University of California Los Angeles and affiliated organizations published data from a study that aimed to identify novel surface proteins that are highly and selectively expressed in tumors and could serve as targets for chimeric antigen receptor (CAR) T-cell therapies for the treatment of melanoma.
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Test tubes with blood samples
Immune

With series A funds, IMU Bio’s Cytatlas identifies cell types and immune signatures

Jan. 24, 2024
By Nuala Moran
IMU Biosciences Ltd. has raised £11.5 million (US$14.7 million) in a series A round to further develop and commercialize profiling technology that can identify from a blood sample which of more than 2,000 cell types are present in an individual’s immune system.
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CAR T cells attacking cancer cell
Drug Design, Drug Delivery & Technologies

Enhancing CAR T cells with degraders and ligases

Dec. 1, 2023
By Mar de Miguel
Researchers have developed a new approach for the development of improved CAR T cells with bifunctional degraders, which linked ubiquitin to an endogenous target protein. The key to the design was the use of multispecific protein degraders and E3 ligases, which increased the proliferation of CAR T cells and their antitumor potency. This combination can be adapted to different uses of cell therapies.
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