Recent blog posts
Alnylam Unveils Phase 3 HELIOS-B Study Results of Vutrisiran in ATTR Cardiomyopathy at ESC Congress
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Alnylam Unveils Phase 3 HELIOS-B Study Results of Vutrisiran in ATTR Cardiomyopathy at ESC Congress
4 September 2024
Alnylam Shares In-Depth Findings from Successful Phase 3 HELIOS-B Study of Vutrisiran in ATTR Amyloidosis Cardiomyopathy Patients at ESC Congress.
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Orgenesis Announces Positive Results from ORG-101 CAR-T Study in CD19+ Acute Lymphoblastic Leukemia
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Orgenesis Announces Positive Results from ORG-101 CAR-T Study in CD19+ Acute Lymphoblastic Leukemia
4 September 2024
Orgenesis Reports Favorable Outcomes from a Practical Study on ORG-101 CAR-T Treatment in CD19+ Acute Lymphoblastic Leukemia Patients.
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Johnson & Johnson Seeks Initial Approval for Nipocalimab in Treating Broad-Spectrum Myasthenia Gravis
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Johnson & Johnson Seeks Initial Approval for Nipocalimab in Treating Broad-Spectrum Myasthenia Gravis
4 September 2024
Johnson & Johnson aims for initial approval of nipocalimab to treat a wide range of patients with antibody-positive generalized myasthenia gravis.
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Merck Releases Progress Report for Phase 3 Studies: KEYNOTE-867 & KEYNOTE-630 Clinical Trials
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Merck Releases Progress Report for Phase 3 Studies: KEYNOTE-867 & KEYNOTE-630 Clinical Trials
3 September 2024
Merck has recently divulged advancements pertaining to two pivotal Phase 3 clinical trials, designated as KEYNOTE-867 and KEYNOTE-630.
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Rallybio Reveals Phase 1 Results of RLYB212 in Blood Clotting Dynamics
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Rallybio Reveals Phase 1 Results of RLYB212 in Blood Clotting Dynamics
3 September 2024
Rallybio Unveils RLYB212's Phase 1 Exploratory Study Outcomes in Blood Clotting & Coagulation Dynamics.
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Bayer Initiates Stage III Assessment for Non-Small Cell Lung Cancer (NSCLC) Treatment
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Bayer Initiates Stage III Assessment for Non-Small Cell Lung Cancer (NSCLC) Treatment
3 September 2024
Bayer has disclosed the enrollment of the inaugural patient into the international Phase III SOHO-02 study, a randomized, open-label, multicenter clinical endeavor.
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Merck KGaA Begins Phase III Trial of Oral Cladribine for gMG in Germany
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Merck KGaA Begins Phase III Trial of Oral Cladribine for gMG in Germany
3 September 2024
Merck KGaA, headquartered in Darmstadt, Germany, Reveals Initiation of Phase III Trial with Oral Cladribine for Treating Generalized Myasthenia Gravis (gMG), Marking First Patient Administration.
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Biocon Biologics Secures Market Access for Biosimilar Bmab 1200 in Europe, UK, Canada, and Japan
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Biocon Biologics Secures Market Access for Biosimilar Bmab 1200 in Europe, UK, Canada, and Japan
3 September 2024
Biocon Biologics Achieves Market Access for Bmab 1200, a Biosimilar Candidate Akin to Stelara®, Across Europe, the UK, Canada, and Japan.
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Jeune Aesthetics Reports Positive Phase 1 Results for KB301 in Reducing Eye and Décolletage Wrinkles
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Jeune Aesthetics Reports Positive Phase 1 Results for KB301 in Reducing Eye and Décolletage Wrinkles
3 September 2024
Jeune Aesthetics Reveals Encouraging Interim Safety & Efficacy Outcomes for KB301 in Phase 1, Targeting Lateral Eye Creases & Active Décolletage Wrinkles Reduction.
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Encouraging Phase 2 Results of NBI-1117568 in Adult Schizophrenia Show Potential Efficacy
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Encouraging Phase 2 Results of NBI-1117568 in Adult Schizophrenia Show Potential Efficacy
3 September 2024
Neurocrine Biosciences Announces Encouraging Phase 2 Outcomes for NBI-1117568 in Adult Schizophrenia Patients, Demonstrating Potential Efficacy.
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Novartis' Leqvio® Significantly Reduces LDL-C in Low to Moderate ASCVD Risk Patients as Standalone Treatment
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Novartis' Leqvio® Significantly Reduces LDL-C in Low to Moderate ASCVD Risk Patients as Standalone Treatment
30 August 2024
Novartis' biannual Leqvio® showed significant and meaningful LDL-C reduction as a solo treatment for patients with low to moderate ASCVD risk.
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Merck Initiates Phase 3 Trial for Bomedemstat in Select Essential Thrombocythemia Cases
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Merck Initiates Phase 3 Trial for Bomedemstat in Select Essential Thrombocythemia Cases
30 August 2024
Merck Begins Phase 3 Study of Bomedemstat, an Experimental Drug for Specific Essential Thrombocythemia Patients.
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