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BioWorld - Tuesday, December 30, 2025
Home » Topics » Series A, BioWorld

Series A, BioWorld
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Aavantibio, with help from Sarepta, comes on with a $105M series A

Oct. 22, 2020
By Lee Landenberger
Aavantibio Inc., with the help of a large check from Sarepta Therapeutics Inc., has launched with a $107 million series A to pursue gene therapies for treating rare genetic diseases. The lead program is in Friedreich’s ataxia (FA), a rare genetic disease that typically begins in childhood and causes progressive damage to the nervous system.
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Hand holding gear, dollar sign

Dren’s $60M series A to propel it through preclinical development

Oct. 19, 2020
By Lee Landenberger
Dren Bio Inc. has closed on a $60 million series A to push its two lead programs through early clinical development. The company’s DR-01 is an antibody-based therapy for treating rare leukemias, lymphomas and specific phenotypes of autoimmune disorders. The company said it is initially targeting neglected hematology-oncology indications.
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Dollar sign in piggy bank

Radioheads: Rayzebio closes $45M for targeted radiopharmaceuticals

Oct. 14, 2020
By Cormac Sheridan
Rayzebio Inc. raised $45 million in a series A round to build a platform company focused on developing targeted radiopharmaceuticals for solid tumor indications.
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More cashflow: Rappta Therapeutics, Chord Therapeutics close series A rounds

Oct. 13, 2020
By Cormac Sheridan
DUBLIN – The cash spigot is still turned on, as two more European firms disclosed series A rounds on Oct. 13. Chord Therapeutics SA took in €16 million (US$18.8 million) to repurpose cladribine for rare autoimmune disorders. Rappta Therapeutics Oy raised €9 million to take forward a novel concept in cancer, focused on developing small-molecule activators of protein phosphatase 2A (PP2A).
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Acute myeloid leukemia illustration

Priothera closes $35M series A round for pivotal trial to boost HSCT outcomes in AML

Oct. 12, 2020
By Cormac Sheridan
DUBLIN – Priothera Ltd. closed a €30 million (US$35.4 million) series A round to shepherd an oral sphingosine 1 phosphate (S1P) receptor agonist through clinical development in patients with acute myeloid leukemia (AML) who are undergoing allogeneic hematopoietic stem cell transplantation (HSCT).
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Trekkies delight: Federation launches with a $50M series A

Oct. 6, 2020
By Lee Landenberger
Federation Bio Inc., which just closed a $50 million series A, had enough preclinical data in engineering bacteria to drive the immune system up or down that it actually could have become two separate companies, its new CEO told BioWorld.
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Gene editing illustration

Starting with Biogen deal in ALS, Scribe planning a new chapter in CRISPR story

Oct. 6, 2020
By Cormac Sheridan
Scribe Therapeutics Inc., another CRISPR-based genome editing firm out of the Jennifer Doudna stable, launched with $20 million in series A funding and a deal with Biogen Inc. in amyotrophic lateral sclerosis (ALS), which brings in another $15 million up front and up to $400 million in development and commercial milestones.
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Bioshin rakes in $60M in series A funding led by Orbimed

Sep. 30, 2020
By Gina Lee
HONG KONG – Shanghai-based Bioshin Ltd., the Asia-Pacific arm of New Haven, Conn.-based Biohaven Pharmaceutical Holding Co. Ltd., has added $60 million to its war chest via a series A investment.
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Hand holding money plant

Ena Respiratory launches with AU$11.7M series A as it heads toward clinic with COVID-19 nasal spray

Sep. 28, 2020
By Tamra Sami
PERTH, Australia – Australia’s largest health care venture capital firm, Brandon Capital, announced the launch of Australian biotech company Ena Respiratory Pty Ltd., which has developed a nasal treatment to boost the natural immune system to fight common colds and flu and has proved successful in reducing COVID-19 viral replication.
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Isaac Veinbergs, CEO, Libra Therapeutics
Newco news

Libra launches with a $29M series A to treat neurodegenerative diseases

Sep. 23, 2020
By Lee Landenberger
In the past 10 years, the advances in understanding the etiology of neurodegenerative diseases have been dramatic. “The development of novel biomarkers and other tools as well are key in aiding diagnostic potential and the ability to track disease progression have been phenomenal,” Isaac Veinbergs, CEO of newly created Libra Therapeutics Inc., told BioWorld.
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