News about "New England Journal of Medicine"

Eli Lilly and Company Reports Strong LDL-C Reduction with One-Time PCSK9 Gene Editing Therapy VERVE-102

Eli Lilly and Company Reports Strong LDL-C Reduction with One-Time PCSK9 Gene Editing Therapy VERVE-102

Eli Lilly and Company reports that a single dose of investigational gene-editing therapy VERVE-102 delivered sustained reductions in PCSK9 and LDL cholesterol for up to 18 months in high-risk cardiovascular patients.

New England Journal Of Medicine | 26/05/2026 | By News Bureau 217

Bayer Wins US FDA Priority Review for Asundexian Stroke Prevention Therapy

Bayer Wins US FDA Priority Review for Asundexian Stroke Prevention Therapy

Bayer receives US Food and Drug Administration Priority Review (PR) for asundexian to reduce recurrent stroke risk after non-cardioembolic ischemic stroke or transient ischemic attack, supported by positive phase 3 OCEANIC-STROKE trial results.

New England Journal Of Medicine | 20/05/2026 | By News Bureau

Bristol Myers Squibb Reports Positive Phase 3 SCOUT-HCM Trial Results

Bristol Myers Squibb Reports Positive Phase 3 SCOUT-HCM Trial Results

Bristol Myers Squibb reports positive Phase 3 SCOUT-HCM results showing Camzyos efficacy and safety in adolescents with oHCM, achieving significant LVOT reduction with no new safety concerns.

New England Journal Of Medicine | 30/03/2026 | By News Bureau 102

Bayer Secures Japanese Approval for Finerenone

Bayer Secures Japanese Approval for Finerenone

Bayer has received approval from Japan’s Ministry of Health, Labour and Welfare (MHLW) for Finerenone (Kerendia), a non-steroidal, selective mineralocorticoid receptor antagonist, for the treatment of adult patients with chronic heart failure with mildly reduced or preserved Left Ventricular Ejection Fraction (LVEF).

New England Journal Of Medicine | 23/12/2025 | By News Bureau 434

FDA Approves Diagnostic Tool for Pembrolizumab Combo in Endometrial Cancer

FDA Approves Diagnostic Tool for Pembrolizumab Combo in Endometrial Cancer

The US FDA has cleared the OncoMate MSI Dx Analysis System as a companion diagnostic to guide pembrolizumab-based combination therapy in advanced endometrial cancer. The PCR-based assay determines microsatellite instability (MSI) status in tumour tissue, with support from Merck, developer of pembrolizumab and lenvatinib.

New England Journal Of Medicine | 15/11/2025 | By Dineshwori 310


 

 

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