Category News

Nanoemulsions Market Report 2024-2030: Analysis & Forecasts by Drug Class

Global Nanoemulsions Market Report 2024-2030: Growth Trends, Applications, and Forecasts Nanoemulsions – Global Strategic Business Report,” providing an in-depth analysis of the expanding nanoemulsions market. This report examines industry trends, market drivers, and forecasts, offering valuable insights for businesses and…

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ENHERTU® Approved in U.S. for HER2-Low Metastatic Breast Cancer Post-Endocrine Therapy

ENHERTU® Approved in U.S. for HER2-Low Metastatic Breast Cancer Post-Endocrine Therapy Daiichi Sankyo (TSE: 4568) and AstraZeneca’s (LSE/STO/Nasdaq: AZN) ENHERTU® (fam-trastuzumab deruxtecan-nxki) has been approved in the U.S. for the treatment of adult patients with unresectable or metastatic hormone receptor (HR)…

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Phase 2 Trial: Cytokinetics Launches AMBER-HFpEF Study of CK-586 in Symptomatic HFpEF

Introduction: Cytokinetics Advances CK-586 into Phase 2 Trial Cytokinetics, Incorporated a leading biopharmaceutical company, has announced that enrollment is now open for AMBER-HFpEF, a pivotal Phase 2 clinical trial evaluating CK-586 in patients with symptomatic heart failure with preserved ejection…

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Poxel Secures Patent in China for Imeglimin Use in Type-2 Diabetic Patients with Renal Impairment

Poxel Advances Global Strategy with Key Patent for Imeglimin in China Expanding Innovative Treatments for Chronic Metabolic Diseases Poxel, a clinical-stage biopharmaceutical company focused on developing cutting-edge treatments for chronic diseases with metabolic origins, has reached a significant milestone in…

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Blueprint Medicines Shares 2025 Outlook and Strategic Plans for Sustained Growth

Blueprint Medicines Corporation recently unveiled its 2025 corporate outlook and strategic vision for sustained growth, leveraging its established research, development, and commercial expertise. According to Kate Haviland, Chief Executive Officer of Blueprint Medicines, the company enters 2025 stronger than ever,…

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Osimertinib Compared to RYBREVANT® + LAZCLUZE™ Significant and Promising Survival Benefit Observed

Osimertinib: A Benchmark in Targeted Therapy Osimertinib The European Commission has granted approval for the combination of RYBREVANT® (amivantamab) and LAZCLUZE® (lazertinib) for the first-line treatment of adult patients with advanced non-small cell lung cancer (NSCLC) who harbor EGFR exon…

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Promising Formulation of New Sarclisa Subcutaneous Treatment Meets Co-Primary Endpoints in IRAKLIA Phase 3

Formulation Results from the IRAKLIA Phase 3 Study Demonstrate Promise for Subcutaneous Sarclisa in Multiple Myeloma The Formulation IRAKLIA Phase 3 study has presented encouraging results for the investigational subcutaneous (SC) formulation of Sarclisa, administered through an on-body delivery system…

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