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FDA Approves Vertex's Clinical Trials for ADPKD Drug VX-407
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FDA Approves Vertex's Clinical Trials for ADPKD Drug VX-407
26 March 2024
Vertex has received authorization from the FDA to proceed with clinical trials for VX-407, a new drug candidate targeting the management of ADPKD.
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Sosei Heptares Regains Full Rights to Oral GPR35 Activator HTL0027477 from GSK for Inflammatory Bowel Trials
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Sosei Heptares Regains Full Rights to Oral GPR35 Activator HTL0027477 from GSK for Inflammatory Bowel Trials
26 March 2024
Sosei Heptares reclaims complete control over HTL0027477 from GSK, a pioneering oral GPR35 activator set for clinical trials in treating inflammatory bowel conditions.
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Promising Early Results for ACELYRIN's Lonigutamab in Thyroid Eye Disease Studies
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Promising Early Results for ACELYRIN's Lonigutamab in Thyroid Eye Disease Studies
26 March 2024
ACELYRIN, INC. has revealed encouraging initial data from its Phase 1/2 studies for Lonigutamab. This first-of-its-kind, injectable treatment targeting IGF-1R has shown promising therapeutic effects in patients suffering from Thyroid Eye Disease.
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Entera Bio Reveals Promising Oral GLP-2 Pill Efficacy for Short Gut Syndrome
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Entera Bio Reveals Promising Oral GLP-2 Pill Efficacy for Short Gut Syndrome
24 March 2024
Entera Bio Unveils Strong Drug Absorption Results for Innovative Oral GLP-2 Hormone Pill Designed for Individuals with Short Gut Condition.
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23andMe Initiates Clinical Trial of Dual-Targeting Antibody 23ME-01473 Against ULBP6
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23andMe Initiates Clinical Trial of Dual-Targeting Antibody 23ME-01473 Against ULBP6
24 March 2024
23andMe Commences Early-Stage Clinical Evaluation of Its Bifunctional Antibody, 23ME-01473, Aimed at ULBP6.
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Nurix Reveals NX-1607, a Novel CBL-B Inhibitor, at ACS Conference
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Nurix Reveals NX-1607, a Novel CBL-B Inhibitor, at ACS Conference
24 March 2024
Nurix Unveils the Innovation and Molecular Configuration of Pioneering CBL-B Suppressant NX-1607 during the ACS Conference.
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CheckMate -9DW Success: Opdivo and Yervoy Boost Survival in Progressive Liver Cancer
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CheckMate -9DW Success: Opdivo and Yervoy Boost Survival in Progressive Liver Cancer
22 March 2024
Bristol Myers Squibb Reveals Successful Outcome for CheckMate -9DW Study Assessing the Combination of Opdivo and Yervoy in Extending Survival in Initial Therapy of Progressive Liver Cancer.
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FDA Approves Idorsia's TRYVIO, First Endothelin Antagonist for Resistant Hypertension
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FDA Approves Idorsia's TRYVIO, First Endothelin Antagonist for Resistant Hypertension
22 March 2024
The FDA has approved Idorsia's daily drug TRYVIO (aprocitentan), the first to use an endothelin receptor antagonist for managing resistant hypertension alongside other medications.
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Mabwell's Novel ADC Targets Nectin-4, Shows Promise in Cervical Cancer Treatment
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Mabwell's Novel ADC Targets Nectin-4, Shows Promise in Cervical Cancer Treatment
22 March 2024
Mabwell's novel antibody-drug conjugate targeting Nectin-4 in cervical cancer shows significant treatment promise according to initial clinical findings.
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Reddy’s Labs introduces Versavo® (bevacizumab) to the UK market
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Reddy’s Labs introduces Versavo® (bevacizumab) to the UK market
22 March 2024
Dr. Reddy’s Laboratories Ltd., an international enterprise specializing in pharmaceuticals, has officially declared the introduction of its drug Versavo® (bevacizumab) to the UK market.
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Orchard Therapeutics Gains FDA Approval for Lenmeldy™ (atidarsagene autotemcel) for Early-Stage Metachromatic Leukodystrophy in Children
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Orchard Therapeutics Gains FDA Approval for Lenmeldy™ (atidarsagene autotemcel) for Early-Stage Metachromatic Leukodystrophy in Children
22 March 2024
Orchard Therapeutics has obtained U.S. FDA endorsement for Lenmeldy™, a proprietary treatment branded as atidarsagene autotemcel, designed exclusively for young patients diagnosed with early-stage Metachromatic Leukodystrophy.
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Actinium-Based PSMA Radioconjugate Deal Targets Prostate Cancer Treatment and Development
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Actinium-Based PSMA Radioconjugate Deal Targets Prostate Cancer Treatment and Development
22 March 2024
The deal encompasses a clinical-phase actinium radioconjugate aimed at PSMA to combat prostate cancer, a collection of radioconjugate products in development, and cutting-edge research, development, and production infrastructure.
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