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BioWorld - Monday, January 26, 2026
Home » Topics » Series A, BioWorld

Series A, BioWorld
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Skeletal disorder firm Innoskel launches with $24M

Dec. 14, 2020
By Nuala Moran
LONDON – Innoskel has arrived on the scene with a €20 million (US$24.3 million) series A funding to advance development of gene therapies for type 2 collagenopathies, a group of rare skeletal disorders that affect the structure of connective tissues, leading to short stature.
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Dollar sign in piggy bank

Remix raises $65M series A to develop RNA modulators

Dec. 8, 2020
By Michael Fitzhugh
Remix Therapeutics Inc., a Cambridge, Mass.-based startup developing small-molecule RNA modulators, said it has raised $65 million in series A financing led by Foresite Capital.
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Evan Feinberg, CEO and co-founder, Genesis

Near its beginning, Genesis brings in a $52M series A

Dec. 2, 2020
By Lee Landenberger
Genesis Therapeutics Inc. CEO and co-founder Evan Feinberg likens the collaboration of his company’s team of chemists, biologists and software developers to that of a jazz band. Everyone has to be familiar with everyone else’s roles and responsibilities in order to do their job, or play a solo, when it’s their turn.
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Macrophage illustration

Resolution raises $36M series A for macrophage cell therapy in liver cirrhosis

Dec. 2, 2020
By Nuala Moran
LONDON – Syncona Ltd. has unveiled its fifth cell therapy startup, Resolution Therapeutics Ltd., which arrives on the scene with a £26.6 million (US$35.6 million) series A to exploit the ability of macrophages to stimulate liver repair.
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3D Euro symbol
Newco news

Noema raises $60M to move Roche assets into orphan CNS indications

Dec. 1, 2020
By Cormac Sheridan
DUBLIN – Noema Pharma AG closed a €54 million (US$59.8 million) series A round to take forward four clinical-stage assets it has in-licensed from Roche Holding AG. The drug candidates are being lined up for orphan neurological indications that fall outside of Roche’s strategic focus.
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T cells

Anchors aweigh: Catamaran Bio sets sail with $42M to develop allogeneic CAR-NK cell therapies

Nov. 23, 2020
By Cormac Sheridan
When the first chimeric antigen receptor T-cell (CAR T) therapy, Kymriah (tisagenlecleucel), was approved in 2016 for treating B-cell acute lymphoblastic leukemia, its developer, Novartis AG, confined the initial rollout to just 20 treating centers. Its label carried a black box warning, because of the risk of life-threatening cytokine release syndrome, and Basel, Switzerland-based Novartis put in place a comprehensive risk evaluation and mitigation system to ensure its safe use. Catamaran Bio Inc., a Boston-based startup that has raised $42 million in seed and series A financing, is considering the administration of similarly engineered natural killer cells in walk-in clinics. “If the product is safe, it can be given as an out-patient treatment,” Chief Scientific Officer Vipin Suri told BioWorld. “As a field, this absolutely has to be our ambition.”
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George Chen, co-founder, chairman and CEO, D3 Bio

D3 Bio launches with a hefty $200M series A financing

Nov. 20, 2020
By David Ho
HONG KONG – D3 Bio Inc. is the new kid on the biopharma block in Shanghai, kicking off with a $200 million series A financing backed by some of Asia’s most prominent venture capital firms.
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3D Euro symbol

Celleron spin-out Synox raises $44M for pivotal trial of emactuzumab

Nov. 19, 2020
By Cormac Sheridan
DUBLIN – Synox Therapeutics Ltd., a spin-out from Celleron Therapeutics Ltd., has raised €37 million (US$43.7 million) in a series A round to conduct a pivotal trial of emactuzumab, an antibody its parent company in-licensed from Roche Holding AG in August.
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Syncona’s kidney disease gene therapy play: Purespring seeks answers to $60M questions

Nov. 19, 2020
By Cormac Sheridan
DUBLIN – Health care investor Syncona Ltd. has founded a new startup, Purespring Therapeutics Ltd., to take gene therapy into the kidney. It is committing £45 million (US$59.6 million) in series A funding, which will support the build-out of the new company and take at least one program into the clinic.
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Metagenomi launches with $65M series A and long leash in gene editing

Nov. 12, 2020
By Lee Landenberger
Metagenomi Inc. has raised a $65 million series A financing to expand its gene editing abilities, advance its research and validate its pipeline in preclinical studies. The company’s CRISPR-based systems use algorithms for screening thousands of genomes from microorganisms to advance therapies for use in oncology, genetic diseases and possibly much more.
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