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BioWorld - Wednesday, April 22, 2026
Home » Topics » Cell therapy, BioWorld

Cell therapy, BioWorld
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Ayele Dilion Mashiah, CEO, Remedy
Newco news

Remedy pushes ‘cell-free’ secretome therapy for IPF into phase I

April 15, 2026
By Marian (YoonJee) Chu
No Comments
“Single drugs targeting single biological pathways are insufficient for complex diseases,” Remedy Cell Ltd. CEO Ayelet Dilion Mashiah told BioWorld. Remedy is taking a secretome-based approach to treat lung disorders, having moved its lead asset, RC-0315, into a first-in-human clinical trial for idiopathic pulmonary fibrosis (IPF) in January. Secretomes refer to the collection of bioactive molecules secreted by cells in the extracellular space, including proteins, enzymes, growth factors and extracellular vesicles such as exosomes.
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Cell therapy illustration
Newco news

‘Immune reset’ is ambition of Tr1x’s allogenic Tr1 cell therapy

April 14, 2026
By Marian (YoonJee) Chu
No Comments
Tr1x Inc. was founded with a simple but ambitious goal: to change how autoimmune and inflammatory diseases are treated, moving away from chronic treatment and toward durable cures. “We are trying to flip the script on regulatory T cells (Tregs),” Tr1x CEO David de Vries told BioWorld. “The goal is to reset the immune system rather than continuously suppress it, and we believe we have a unique technology to do that.”
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Blue-gray dollar sign
Newco news

Excalipoint closes $68.7M seed round for cancer T-cell engagers

March 18, 2026
By Marian (YoonJee) Chu
No Comments
Excalipoint Therapeutics Inc. launched with an oversubscribed $68.7 million seed financing round to advance a portfolio of T-cell engagers for solid tumors, marking one of the largest early stage financings in China biotech history.
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Induced pluripotent stem cells

Japan approves first iPSC therapy for Parkinson’s disease

March 6, 2026
By Tamra Sami
No Comments
Japan has approved the world’s first therapies derived from induced pluripotent stem cells (iPSCs), marking a major milestone for regenerative medicine and, potentially, a turning point in treating Parkinson’s disease.
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Magnifying glass, clock and capsules

FDA’s rare disease toolbox not fully used

March 4, 2026
By Mari Serebrov
No Comments
At the current pace of innovation in the U.S. rare disease space, developing and approving therapies for just half of the 10,000-plus known rare diseases would take more than 160 years, Bradley Campbell, president and CEO of Amicus Therapeutics Inc., recently told the Senate Committee on Aging.
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CAR T cell attacking cancer cells
Immuno-oncology

HITting solid tumors with a closer look and a stronger CAR T cell

March 2, 2026
By Anette Breindl
No Comments
CAR T cells have been groundbreaking for the treatment of B-cell cancers. But 8 years after Kymriah (tisagenlecleucel, Novartis AG) became the first CAR T-cell therapy to be approved, there are no CAR Ts approved for solid tumors.
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Patent gears

US Fed Circuit protects 101 passage for some gene therapy patents

Feb. 24, 2026
By Mari Serebrov
No Comments
In handing a win to Regenxbio Inc., the U.S. Court of Appeals for the Federal Circuit also cleared some leaves from the 101 patent eligibility threshold after years of Supreme Court decisions cluttering the passageway.
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Glass yen/yuan symbol

Innovacell’s $91M Tokyo IPO to fund incontinence cell therapies

Feb. 24, 2026
By Marian (YoonJee) Chu
No Comments
Innovacell Inc. launched a ¥14.16 billion (US$91.2 million) stock sale on the Tokyo Stock Exchange Feb. 24, ending a near two-year lull of biotech listings in Japan while signaling a dynamic year ahead for cell-based therapeutics.
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Astellas global HQ in Tokyo

Astellas and Vir in $1.3B deal for CD3 T-cell engager

Feb. 24, 2026
By Tamra Sami
No Comments
Astellas Pharma Inc. and Vir Biotechnology Inc. have signed a global co-development pact to advance VIR-5500, Vir’s PRO-XTEN dual-masked CD3 T-cell engager targeting prostate-specific membrane antigen for treating prostate cancer. Under the deal terms, San Francisco-based Vir will receive $335 million in up-front and near-term payments, including $240 million in cash, $75 million in equity investment and a $20 million near-term milestone. Vir is also eligible to receive up to $1.37 billion in development, regulatory and sales-based milestones plus royalties on ex-U.S. sales.
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Green arrow up red arrow down

Bladder phase II sinks Protara, LMs phase III wins for Palvella

Feb. 24, 2026
By Randy Osborne
No Comments
Almost three months to the day after Protara Therapeutics Inc. made known positive interim data from the phase II trial testing cell-based therapy TARA-002 in pediatric patients with macrocystic and mixed cystic lymphatic malformations (LMs), Palvella Therapeutics Inc. scored positive top-line results from the phase III Selva study evaluating Qtorin 3.9% rapamycin anhydrous gel for microcystic LMs.
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