Dark Blue Therapeutics Ltd

United Kingdomdarkbluetx.com

Dark Blue Therapeutics Ltd is a biotechnology company based in Oxford, UK, founded in 2020 as a spinout from the University of Oxford. The company specializes in precision oncology, developing first-in-class small-molecule therapies that target novel cancer vulnerabilities, including protein degraders.

Its lead candidate, DBT-3757, is a targeted protein degrader of MLLT1/3 proteins, advancing through IND-enabling studies for the treatment of acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL). The preclinical program demonstrates promising anti-cancer activity and potential as a single-agent therapy.

In January 2026, Dark Blue Therapeutics was acquired by Amgen in a deal valued at up to $840 million, integrating its pipeline into Amgen's oncology research efforts to address unmet needs in difficult-to-treat cancers like AML.

Latest news on Dark Blue Therapeutics

7 June 2026
Amgen: Repatha (evolocumab) cuts first major CV events 29% in high‑risk diabetes subgroup

VESALIUS‑CV subgroup shows evolocumab lowers first major cardiovascular events and LDL‑C; real‑world GLP‑1 persistence is low, curbing potential benefits.

19 May 2026
Amgen CFO Peter Griffith to retire; Thomas Dittrich named CFO

Successor returns July 1 as EVP and assumes CFO duties Sept 1; outgoing CFO stays through Jan 2027 to aid transition. Successor has 30+ yrs finance leadership, ex‑CFO at Galderma, Shire, Sulzer.

4 May 2026
Amgen invests $300M more in U.S. manufacturing, nearly $2B over past year

Expands Puerto Rico biologics facility to boost U.S. production, deploy next‑gen technologies, support workforce development and construction jobs, and strengthen medicine supply‑chain resilience

22 April 2026
Amgen EVP & CTO David M. Reese to retire

Reese retires June 30, 2026. Effective June 1, leadership reshuffle: James Bradner named EVP R&D, AI & Data; Sean Bruich CTO; Murdo Gordon EVP Global Markets & Policy; Paul Burton remains CMO.

28 March 2026
Amgen: Repatha cuts first major cardiovascular events 31% in high‑risk patients without significant atherosclerosis

VESALIUS‑CV subgroup (3,655 high‑risk diabetics without known atherosclerosis) showed a 31% reduction in first major CV events vs placebo; median LDL‑C 44 mg/dL over ~4.8 years.