Recent blog posts
Senti Bio Initiates Phase 1 Trial of SENTI-202 for Recurrent or Treatment-Resistant Blood Cancers
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Senti Bio Initiates Phase 1 Trial of SENTI-202 for Recurrent or Treatment-Resistant Blood Cancers
15 May 2024
Senti Bio reports initial dosing in a Phase 1 trial for SENTI-202, targeting recurrent or treatment-resistant blood cancers like Acute Myeloid Leukemia.
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Novo Nordisk's Mim8 Treatments Significantly Reduce Bleeding Episodes in Haemophilia A Patients in Frontier 2 Study
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Novo Nordisk's Mim8 Treatments Significantly Reduce Bleeding Episodes in Haemophilia A Patients in Frontier 2 Study
15 May 2024
Novo Nordisk A/S reports that in the Frontier 2 study, their once-weekly and once-monthly Mim8 treatments significantly outperformed standard and prior prophylaxis treatments in reducing bleeding episodes in individuals with haemophilia A.
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Mabwell Reports Advancement in 9MW2821 Clinical Trials for Triple-Negative Breast Cancer
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Mabwell Reports Advancement in 9MW2821 Clinical Trials for Triple-Negative Breast Cancer
15 May 2024
Mabwell reported progress in its clinical trial of the novel Nectin-4 targeting ADC (9MW2821) for triple-negative breast cancer treatment.
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AC Immune and Takeda Strike Exclusive Licensing Deal on Alzheimer’s Amyloid Beta Immunotherapy
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AC Immune and Takeda Strike Exclusive Licensing Deal on Alzheimer’s Amyloid Beta Immunotherapy
15 May 2024
AC Immune and Takeda Enter an Exclusive Deal for Licence and Option on Active Immunotherapy Focused on Amyloid Beta for Alzheimer's Disease.
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Kodiak Sciences Initiates Phase 3 GLOW2 Study on Tarcocimab Tedromer for Diabetic Retinopathy
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Kodiak Sciences Initiates Phase 3 GLOW2 Study on Tarcocimab Tedromer for Diabetic Retinopathy
15 May 2024
Kodiak Sciences has started treating initial participants in the Phase 3 GLOW2 study, examining Tarcocimab Tedromer for diabetic retinopathy.
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Ajax Therapeutics Gains FDA Approval for New Myelofibrosis Drug AJ1-11095
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Ajax Therapeutics Gains FDA Approval for New Myelofibrosis Drug AJ1-11095
15 May 2024
Ajax Therapeutics has received FDA approval for its investigational new drug application for AJ1-11095, a novel Type II JAK2 inhibitor, intended for the management of myelofibrosis.
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FDA Prioritizes Review of Dupixent® for Teen Chronic Sinusitis and Nasal Polyps
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FDA Prioritizes Review of Dupixent® for Teen Chronic Sinusitis and Nasal Polyps
15 May 2024
FDA grants priority review to Dupixent® (dupilumab) sBLA for treating teens with chronic rhinosinusitis and nasal polyps.
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Promising Phase 2a Results for Cardurion's Heart Failure Treatment
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Promising Phase 2a Results for Cardurion's Heart Failure Treatment
15 May 2024
Cardurion Pharmaceuticals Reports Encouraging Outcomes from Phase 2a CARDINAL-HF Study of PDE9 Inhibitor in Heart Failure Patients.
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AnaptysBio Announces Positive Early Results from Phase 3 GEMINI-2 Study of Imsidolimab for Generalized Pustular Psoriasis
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AnaptysBio Announces Positive Early Results from Phase 3 GEMINI-2 Study of Imsidolimab for Generalized Pustular Psoriasis
14 May 2024
Anaptys released encouraging initial outcomes from the GEMINI-2 Phase 3 study of Imsidolimab (IL-36R) for treating Generalized Pustular Psoriasis.
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Fusion Pharmaceuticals Initiates Phase 2 AlphaBreak Trial of FPI-2265 in Metastatic Prostate Cancer
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Fusion Pharmaceuticals Initiates Phase 2 AlphaBreak Trial of FPI-2265 in Metastatic Prostate Cancer
14 May 2024
Fusion Pharmaceuticals revealed that the initial participant has received a dose in the AlphaBreak Trial's Phase 2 study of FPI-2265 for treating metastatic castration-resistant prostate cancer.
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Celltrion USA Launches Cost-Effective Adalimumab Biosimilar as a Budget-Friendly Alternative to HUMIRA®
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Celltrion USA Launches Cost-Effective Adalimumab Biosimilar as a Budget-Friendly Alternative to HUMIRA®
14 May 2024
Celltrion USA now offers a budget-friendly adalimumab-aaty biosimilar as an alternative to HUMIRA® at reduced wholesale prices.
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FDA Grants Approval for WestGene's mRNA Cancer Treatment Vaccine
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FDA Grants Approval for WestGene's mRNA Cancer Treatment Vaccine
14 May 2024
WestGene proudly declares a significant breakthrough as the FDA grants IND approval for its mRNA-based cancer vaccine, WGc-043.
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