ChemoCentryx, Inc.

United Stateschemocentryx.com

ChemoCentryx, Inc. is a biopharmaceutical company headquartered in Mountain View, California. Founded in 1997, it specialized in the discovery, development, and commercialization of orally administered small-molecule therapeutics targeting chemokine and chemoattractant receptors for the treatment of inflammatory diseases, autoimmune disorders, and cancer.

Its lead product, TAVNEOS (avacopan), is an oral complement C5a receptor inhibitor approved as an adjunctive therapy for adults with severe active ANCA-associated vasculitis. In October 2022, ChemoCentryx was acquired by Amgen for approximately $3.7 billion and now operates as a subsidiary, with its assets integrated into Amgen's portfolio.

Latest news on ChemoCentryx

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.