Medical technology company GE HealthCare (Nasdaq:GEHC) announced on Monday that it has agreed to acquire SOFIE Biosciences from Trilantic North America for USD945m in cash, expanding its US radiopharmaceutical manufacturing footprint.
The transaction is expected to close in the first half of 2027, subject to regulatory approvals and other closing conditions, after which SOFIE will become part of GE HealthCare's Pharmaceutical Diagnostics segment.
SOFIE operates a US network of 15 contract manufacturing organisation sites with 21 cyclotrons, as well as a theranostics-focused contract development and manufacturing site. This acquisition is intended to strengthen GE HealthCare's role in the time-critical "final mile" of PET radiopharmaceutical supply and expand its exposure to high-growth areas beyond its existing portfolio.
The deal also provides GE HealthCare with US rights to FAPI-74, a Phase III F18 PET radiotracer with potential applications across multiple cancer indications. GE HealthCare already holds rights to FAPI-74 outside the United States.
Following the closing, SOFIE will continue operating as an independent manufacturing partner and supply its existing portfolio, including products from other radiopharmaceutical providers.
GE HealthCare expects the acquisition to be accretive to revenue growth, Adjusted EBIT margin and Adjusted EPS in the first full year of ownership.
Innovent expands global Phase 3 study of IBI363/TAK-928 to include non-squamous NSCLC
FDA approves WELIREG and LENVIMA combination for previously treated advanced renal cell carcinoma
AstraZeneca's IMFINZI combination receives US Priority Review for muscle-invasive bladder cancer
UChicago Medicine completes construction phase of new cancer facility
FDA Advisory Committee votes in favour of GRAIL's Galleri multi-cancer early detection test
Astellas doses first patient in Phase 3 lung cancer study
X-Chem and Relay Therapeutics collaborate on Phase 3 milestone
BoomRay enters exclusive radioligand therapy asset global license agreement with Novartis
AbbVie and Iambic agree collaboration for discovery and development of small molecule therapies
Grunenthal to acquire Stivarga cancer treatment
Precigen announces FDA platform technology designation for AdenoVerse
Enhertu recommended for EU approval in early HER2-positive breast cancer
PureTech receives FDA Fast Track designation for LYT-200 in HR-MDS
Coiled Therapeutics completes enrolment in two AO-252 formulation cohorts