FDA approves Freenome colorectal cancer blood test to be marketed by Abbott
The FDA has approved Freenome’s new blood-based colorectal cancer test, SimpleScreen CRC, which Abbott will exclusively market in the U.S.
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The FDA has approved Freenome’s new blood-based colorectal cancer test, SimpleScreen CRC, which Abbott will exclusively market in the U.S.
InnoCare Pharma announced Monday that its oral tyrosine kinase 2 (TYK2) inhibitor fadeucravacitinib met the primary endpoint in a phase 3 trial of adults with moderate-to-severe plaque psoriasis.
After signing a deal worth up to $486 million with Italian biopharma Chiesi to develop its pulmonary arterial hypertension (PAH) candidate seralutinib in 2024, Gossamer Bio has ended the collaboration and licensing agreement.
In a sudden leadership shift, Legend Biotech announced that its CEO, Ying Huang, Ph.D., resigned on Friday, with no permanent replacement yet named.
KFF Health News is working to collect and post approved plans as more states respond to emails and public records requests for their documents.
The tiny federal agency that tracks consumer product safety is pressuring hospitals to turn over patient records from emergency room visits, including about injuries that have nothing to do with consumer products.
Reports on departmental staff numbers and costs.
Argenx is spending $2.2 billion to absorb Forte Biosciences for its phase 2-stage vitiligo and celiac disease drug.
AstraZeneca executives told Fierce they are “very confident” in the pharma’s in-house pipeline of ADCs despite scrapping two candidates that underperformed in the clinic.
J. Yoder et al.
C. Ngoepe et al.
Labcorp is launching the Marker by Labcorp Genetic Health Panel, a new direct-to-consumer genetic testing tool that analyzes 163 genes to determine patients’ risk of over 100 hereditary health conditions.
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This cross-sectional study uses data from the National Cancer Database to examine the association between tobacco smoking cessation and cancer stage among US adults.
This cohort study assesses long-term oncologic and quality-of-life outcomes after transperineal template-guided mapping biopsy in patients with prostate cancer.
This case-control study examines whether financial stressors in the year before death are associated with suicide risk among US veterans.
This secondary analysis of a randomized clinical trial assesses the cost-effectiveness of active surveillance compared with standard surgery among patients with esophageal cancer who achieved a complete clinical response after neoadjuvant chemoradiotherapy.
This post hoc analysis of the MINT randomized clinical trial estimates bayesian posterior risk differences and posterior probabilities that a liberal vs restrictive transfusion strategy is associated with reduced risk of 30-day death or myocardial infarction.
This randomized clinical trial assesses whether intraarterial dexamethasone administered during uterine fibroid embolization reduces postprocedural pain compared with placebo.
This stepped-wedge cluster randomized trial evaluates the effectiveness and sustainability of the World Health Organization multimodal improvement strategy for hand hygiene in Ugandan health care facilities.
This cohort study examines the association between initiation of antipsychotic medication and annual prevalence of pharmacologically treated type 2 diabetes among youths in the Netherlands.
This secondary analysis of a cross-sectional study of older adults examines cardiovascular disease risk factor trends in the US, England, and South Korea.
Crystalys’s dotinurad is currently in pivotal testing for gout, a prevalent inflammatory disorder with few treatment options. The drug has the same mechanism of action as a molecule that Sobi added to its pipeline through a $950 million acquisition. The post Crystalys Therapeutics Tacks On $130M for Pivotal Tests of Gout Drug appeared first on MedCity News .