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BioWorld - Sunday, October 1, 2023
Home » Topics » Drugs » CAR T

CAR T
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ASCO20: Allogene CAR T ‘shelf life’ mulled as early phase I results rival autologous

June 1, 2020
By Randy Osborne
No Comments
Allogene Therapeutics Inc. investors will have to wait for an update in the second half of this year to find out more about whether off-the-shelf ALLO-501 can durably stand up to autologous CAR T-cell therapies, but early data disclosed at the American Society of Clinical Oncology meeting is creating buzz in the meantime.
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CAR T cell attacking cancer cells

Edigene, Immunochina betting on allogeneic CAR T therapy in cancer collaboration

May 28, 2020
By Elise Mak
No Comments
SUZHOU, China – Genome editing startup Edigene Inc. and CAR T developer Immunochina Pharmaceuticals Co. Ltd., both from Beijing, have unveiled joint efforts to develop an allogeneic CAR T therapy for cancer. Terms remain undisclosed.
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Steven Yatomi-Clarke, CEO, Prescient Therapeutics

Australia’s Prescient Therapeutics develops next-gen CAR T therapies with UPenn universal immune receptor

May 27, 2020
By Tamra Sami
No Comments
PERTH, Australia – Melbourne-based Prescient Therapeutics Pty Ltd. is poised to develop next-generation CAR T therapies after signing an exclusive global licensing deal with the University of Pennsylvania for a universal immune receptor technology platform.
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China’s Carsgen set to start trials for first claudin18.2-targeted CAR T-cell therapy

May 26, 2020
By Elise Mak
No Comments
BEIJING – CAR T-cell therapeutics developer Carsgen Therapeutics Co. Ltd., of Shanghai, won IND clearance from the FDA for its first-in-class CT-041 for advanced gastric and pancreatic cancers. The company said it is the first claudin18.2 (CLDN18.2)-targeted CAR T-cell therapy cleared for clinical trials in the world.
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China’s Carsgen set to start trials for first claudin18.2-targeted CAR T-cell therapy

May 21, 2020
By Elise Mak
No Comments
BEIJING – CAR T-cell therapeutics developer Carsgen Therapeutics Co. Ltd., of Shanghai, won IND clearance from the FDA for its first-in-class CT-041 for advanced gastric and pancreatic cancers. The company said it is the first claudin18.2 (CLDN18.2)-targeted CAR T-cell therapy cleared for clinical trials in the world.
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Nasdaq building

China CAR T firm Legend Biotech eyes $100M Nasdaq listing

May 19, 2020
By Elise Mak
No Comments
BEIJING – Legend Biotech Corp., headquartered in Somerset, N.J., filed with the U.S. SEC last week plans to raise up to $100 million to advance its BCMA-targeting CAR T candidate, LCAR-B38M, by listing on Nasdaq. Legend confidentially submitted a draft registration statement to the regulators in March.
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Nasdaq building

China CAR T firm Legend Biotech eyes $100M Nasdaq listing

May 18, 2020
By Elise Mak
No Comments
BEIJING – Legend Biotech Corp., headquartered in Somerset, N.J., filed with the U.S. SEC last week plans to raise up to $100 million to advance its BCMA-targeting CAR T candidate, LCAR-B38M, by listing on Nasdaq. Legend confidentially submitted a draft registration statement to the regulators in March.
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Medicare puzzle

Medicare plan expands access to CAR T, incentivizes new antimicrobials

May 12, 2020
By Mari Serebrov
No Comments
Innovation is being rewarded under Medicare’s proposed fiscal 2021 Inpatient Prospective Payment System (IPPS) that was unveiled Monday. For starters, the Centers for Medicare and Medicaid Services (CMS) is proposing a new Medicare-severity-diagnosis related group (MS-DRG) specifically for CAR T therapies.
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Singapore’s Tessa gains U.S. RMAT designation for CD30 CAR T, expands manufacturing efforts

March 3, 2020
By David Ho
No Comments
HONG KONG – Tessa Therapeutics Pte Ltd.’s CD30 CAR T-cell therapy has been granted a regenerative medicine advanced therapy designation by the U.S. FDA based on data from two independent phase I/II trials.
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Singapore’s Tessa gains U.S. RMAT designation for CD30 CAR T, expands manufacturing efforts

Feb. 28, 2020
By David Ho
No Comments
HONG KONG – Singapore-based Tessa Therapeutics Pte Ltd.’s CD30 CAR T-cell therapy has been granted a regenerative medicine advanced therapy (RMAT) designation by the U.S. FDA based on data from two independent phase I/II trials in patients with relapsed or refractory CD30-positive classical Hodgkin lymphoma.
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