News

Roche's Susvimo FDA Approval Marks New Era in Diabetic Macular Edema Treatment Market | DelveInsight
Diabetic macular edema is a complication that develops from diabetic retinopathy, a widespread consequence of diabetes and a ...
Fierce Pharma2d
J&J joins Argenx, UCB in the myasthenia gravis arena with FDA approval for FcRn blocker Imaavy
While Johnson & Johnson isn't the first to secure FDA approval for an FcRn-blocking antibody in myasthenia gravis, the New ...
Taiwan News3d
Tonix Pharmaceuticals Presented Preclinical Data on Gastric Cancer Models at the American Association for Cancer Research (AACR) 2025 Annual Meeting
TNX-1700 is in preclinical development for gastric and colorectal cancers ...
The Mountaineer16d
Rubio in Paris to meet Macron on Ukraine war
US Secretary of State Marco Rubio was in Paris on Thursday to meet French President Emmanuel Macron about crafting a Ukraine ceasefire, as Washington and Europe seek common ground on ending the ...
C&EN17d
Engineering a Fusion Protein Biomaterial Based on SpyTag/SpyCatcher Bioconjugation of Elastin and Collagen Synthetic Proteins
Following this, we optimized the in vitro bioconjugation process by adjusting the molar ratio of Scl2-ST to ELP-SC to 2:1, maximizing the yield of the fusion protein through the application of ...
news-graphic17d
FDA Approves Self-Injection of Vyvgart Hytrulo
WEDNESDAY, April 16, 2025 (HealthDay News) -- The U.S. Food and Drug Administration has approved a self-injection version of Vyvgart Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) for the ...
The Sun Chronicle18d
FDA OKs trial of pig livers as dialysis-like treatment for liver failure
WASHINGTON (AP) — U.S. researchers will soon test whether livers from a gene-edited pig could treat people with sudden liver failure — by temporarily filtering their blood so their own organ ...
The Daily News18d
Quantum Knight Receives FDA Authorization, Marking Breakthrough in Cryptographic Security
becoming the first standalone encryption solution to receive Authority to Operate (ATO) from the U.S. Food and Drug Administration (FDA) for use in life-critical medical and digital infrastructure.
The Bakersfield Californian19d
Quantum Knight Receives FDA Authorization, Marking Breakthrough in Cryptographic Security
from the U.S. Food and Drug Administration (FDA) for use in life-critical medical and digital infrastructure.
Pharm Exec22d
FDA Grants Full Approval to Bayer’s Vitrakvi for NTRK Gene Fusion-Positive Solid Tumors
Full approval of Vitrakvi was based on results from three clinical trials in patients with unresectable or metastatic NTRK fusion-positive solid tumors. “This first full approval of an NTRK inhibitor ...
PMLiVE22d
Bayer’s Vitrakvi receives full FDA approval for NTRK gene fusion-positive tumours
Bayer’s Vitrakvi (larotrectinib) has been granted traditional approval by the US Food and Drug Administration (FDA) to treat neurotrophic ... Tumours with NTRK gene fusion produce an altered TRK ...
Frontiers22d
Case Report: A case of membranous nephropathy associated with primary Sjögren’s syndrome treated with telitacicept
1 Department of Nephrology, The Affiliated YangMing Hospital of NingBo University (Yuyao People’s Hospital), Ningbo, Zhejiang, China 2 Department of Nephrology, Ningbo No.2 Hospital, Ningbo, Zhejiang, ...