Biopharmaceutical companies Jazz Pharmaceuticals plc (Nasdaq:JAZZ) and Chimerix (Nasdaq:CMRX) on Wednesday announced a definitive agreement for Jazz to acquire Chimerix for USD8.55 per share in cash, totalling approximately USD935m.
This acquisition, approved by both companies, is expected to close in the second quarter of 2025.
Chimerix's lead clinical asset, dordaviprone, is a first-in-class small molecule therapy for H3 K27M-mutant diffuse glioma, a rare and aggressive brain tumour. There are currently no US Food and Drug Administration (FDA)-approved therapies for this condition, with radiation as the standard treatment.
The FDA recently accepted and granted Priority Review to dordaviprone's New Drug Application for recurrent H3 K27M-mutant diffuse glioma, setting a Prescription Drug User Fee Act action date of 18 August 2025. If approved, the drug may qualify for a Rare Pediatric Disease Priority Review Voucher.
Dordaviprone is also being evaluated in a Phase 3 trial for newly diagnosed patients following radiation therapy, potentially expanding its use into front-line treatment. The acquisition provides Jazz Pharmaceuticals with a near-term commercial opportunity in the oncology market.
Jazz will fund the transaction through existing cash and investments. Chimerix shareholders will receive a 72% premium based on the company's closing price on 4 March 2025.
The deal is subject to customary closing conditions, including a majority tender of outstanding shares.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA