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BioWorld - Wednesday, April 8, 2026
Home » Keywords » Creyon Bio Inc.

Items Tagged with 'Creyon Bio Inc.'

ARTICLES

Scientists shaking hands in the lab
Drug design, drug delivery & technologies

With new leadership, Creyon enters a $1B-plus deal with Lilly

May 6, 2025
By Lee Landenberger
Less than a week after announcing it had a new CEO, privately held Creyon Bio Inc. began a licensing and research partnership with Eli Lilly and Co. Creyon is getting $13 million up front and could bring in more than $1 billion in milestone payments. The two plan to find, develop and commercialize RNA-targeted oligonucleotide treatments for a range of diseases.
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With new leadership, Creyon enters a $1B-plus deal with Lilly

May 1, 2025
By Lee Landenberger
Less than a week after announcing it had a new CEO, privately held Creyon Bio Inc. began a licensing and research partnership with Eli Lilly and Co. Creyon is getting $13 million up front and could bring in more than $1 billion in milestone payments. The two plan to find, develop and commercialize RNA-targeted oligonucleotide treatments for a range of diseases.
Read More
Drug design, drug delivery & technologies

Creyon Bio and Lilly partner on RNA-targeted oligonucleotide therapies

April 30, 2025
Creyon Bio Inc. has entered into a global licensing and multitarget research collaboration with Eli Lilly & Co. focused on the discovery, development and commercialization of novel RNA-targeted oligonucleotide therapies for a broad range of diseases.
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Grey dollar sign on grey background

Creyon raises $40M to target roots of disease

March 8, 2022
By Lee Landenberger
Rather than focus on making one drug at a time, Creyon Bio Inc. is taking its more than $40 million in seed and series A financing to build its platform to understand the genetic roots of disease and then create precision medicines. Creyon is creating datasets to engineer RNA-based and single-stranded oligonucleotide-based medicines (OBMs) in addition to DNA and RNA editing systems. Those datasets are tailored to deliver models that create OBMs that are safe and effective for treating both common diseases and rare diseases.
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