Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Sanofi Plans to Acquire Inhibrx Inc for Rare Disease Candidate
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Sanofi Plans to Acquire Inhibrx Inc for Rare Disease Candidate
29 January 2024
Sanofi intends to buy Inhibrx, Inc., bringing a promising rare disease candidate targeting Alpha-1 Antitrypsin Deficiency into its portfolio.
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Strand Therapeutics Granted Authorization for Experimental RNA Drug STX-001, Aimed at Addressing Cancerous Growths
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Strand Therapeutics Granted Authorization for Experimental RNA Drug STX-001, Aimed at Addressing Cancerous Growths
29 January 2024
Strand Therapeutics recently revealed that the FDA has approved its request to commence a Phase 1 clinical trial, marking the initial human study of STX-001.
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Gilead Issues Progress Report for EVOKE-01 Phase 3 Research Trial
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Gilead Issues Progress Report for EVOKE-01 Phase 3 Research Trial
29 January 2024
Gilead Sciences' EVOKE-01 Phase 3 Trial for Metastatic NSCLC Fails to Achieve Primary Endpoint: A Comparison of Trodelvy and Docetaxel.
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Sandoz declares deal to buy CIMERLI® operations from Coherus, reinforcing its foothold in the US sector
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Sandoz declares deal to buy CIMERLI® operations from Coherus, reinforcing its foothold in the US sector
29 January 2024
Sandoz Finalizes USD 170 Million Purchase of Coherus BioSciences' Biosimilar Drug CIMERLI* (ranibizumab-eqrn) in the US
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Phase 3 Study of BNT323/DB-1303 for Advanced Breast Cancer Launched by BioNTech & DualityBio
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Phase 3 Study of BNT323/DB-1303 for Advanced Breast Cancer Launched by BioNTech & DualityBio
29 January 2024
BioNTech and DualityBio have launched a critical Phase 3 study for their therapeutic agent BNT323/DB-1303, targeting advanced breast cancer.
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FDA Approves NK CellTech's Clinical Trials for Therapy NK010
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FDA Approves NK CellTech's Clinical Trials for Therapy NK010
29 January 2024
NK CellTech has received the green light from the Food and Drug Administration (FDA) to initiate clinical trials for its therapy, NK010.
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ProMIS Neurosciences Reaches Significant Progress in Crafting a Treatment-Based Alpha-Synuclein Immunization
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ProMIS Neurosciences Reaches Significant Progress in Crafting a Treatment-Based Alpha-Synuclein Immunization
29 January 2024
ProMIS Neurosciences Inc. has declared the identification of a premier vaccine contender, PMN400.
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AC Immune Set to Reacquire Worldwide Ownership of Crenezumab and Semorinemab
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AC Immune Set to Reacquire Worldwide Ownership of Crenezumab and Semorinemab
29 January 2024
AC Immune SA to Reclaim Global Ownership of Two Therapeutic Antibodies Post-Partnership with Genentech and Roche.
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Ionis Reports Promising Preliminary Results in Phase 3 of OASIS-HAE Trial on Donidalorsen for Genetic Angioedema
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Ionis Reports Promising Preliminary Results in Phase 3 of OASIS-HAE Trial on Donidalorsen for Genetic Angioedema
29 January 2024
Ionis reveals encouraging preliminary outcomes from the third phase of the OASIS-HAE trial, examining the experimental compound donidalorsen in individuals with genetic angioedema.
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CheckMate-8HW: Opdivo & Yervoy Combo Reduces Disease Progression or Fatality by 79% in MSI-H/dMMR Metastatic Colorectal Cancer Patients Compared to Chemotherapy
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CheckMate-8HW: Opdivo & Yervoy Combo Reduces Disease Progression or Fatality by 79% in MSI-H/dMMR Metastatic Colorectal Cancer Patients Compared to Chemotherapy
29 January 2024
In the CheckMate -8HW study, the combination of Opdivo and Yervoy reduced the likelihood of disease advancement or fatality in patients with MSI-H/dMMR metastatic colorectal cancer by 79% when compared to chemotherapy.
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BALVERSA® approved by the U.S. FDA to treat advanced or metastatic bladder cancer with genetic mutations
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BALVERSA® approved by the U.S. FDA to treat advanced or metastatic bladder cancer with genetic mutations
25 January 2024
BALVERSA® gains complete sanction from the U.S. FDA to cure bladder cancer in advanced or metastatic stages with specific genetic changes.
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Exploring the Latest Trispecific Antibody Fusion Protein Deal by Harpoon Therapeutics: A Guide to Rapidly Accessing Transaction Insights
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Exploring the Latest Trispecific Antibody Fusion Protein Deal by Harpoon Therapeutics: A Guide to Rapidly Accessing Transaction Insights
25 January 2024
Merck Sharp & Dohme (MSD) and Harpoon Therapeutics announced a deal for MSD to purchase Harpoon at $23/share, totaling around $680 million in equity.
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