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FDA Greenlights Initial Therapy for Niemann-Pick Type C Disease
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FDA Greenlights Initial Therapy for Niemann-Pick Type C Disease
25 September 2024
The U.S. Food and Drug Administration has greenlit Miplyffa (arimoclomol), an oral drug designed for managing Niemann-Pick disease type C (NPC).
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CHMP Issues Positive Opinion for Samsung Bioepis and Biogen's Biosimilar Aflibercept, OPUVIZ™
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CHMP Issues Positive Opinion for Samsung Bioepis and Biogen's Biosimilar Aflibercept, OPUVIZ™
25 September 2024
OPUVIZ has received a recommendation for approval for adult patients in the treatment of neovascular (wet) age-related macular degeneration (AMD).
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Tolebrutinib Delays Disability Progression by 31% in Phase 3 MS Study
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Tolebrutinib Delays Disability Progression by 31% in Phase 3 MS Study
25 September 2024
Tolebrutinib showed a 31% delay in the onset of confirmed disability progression in a phase 3 study of non-relapsing secondary progressive multiple sclerosis.
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Positive Phase 1a Safety, Tolerability, and PK/PD Results for Tectonic Therapeutic's TX45
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Positive Phase 1a Safety, Tolerability, and PK/PD Results for Tectonic Therapeutic's TX45
24 September 2024
Tectonic Therapeutic Shares Positive Safety, Tolerability, and PK/PD Phase 1a Results for Lead Candidate TX45.
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Promising Phase 1 Results for Trishula Therapeutics' TTX-030 in Metastatic Pancreatic Cancer
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Promising Phase 1 Results for Trishula Therapeutics' TTX-030 in Metastatic Pancreatic Cancer
24 September 2024
Trishula Therapeutics' Phase 1 trial of TTX-030 shows encouraging results for first-line treatment of metastatic pancreatic cancer.
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Beacon Therapeutics Releases 36-Month Data on AGTC-501 from HORIZON Phase I/2 Trial for XLRP
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Beacon Therapeutics Releases 36-Month Data on AGTC-501 from HORIZON Phase I/2 Trial for XLRP
24 September 2024
Beacon Therapeutics Shares 36-Month Interim Data from HORIZON Phase I/2 Trial of AGTC-501 for XLRP Patients.
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RYBREVANT® Approved in U.S. as Exclusive Second-Line Targeted Treatment for EGFR-Mutated Advanced Lung Cancer
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RYBREVANT® Approved in U.S. as Exclusive Second-Line Targeted Treatment for EGFR-Mutated Advanced Lung Cancer
24 September 2024
RYBREVANT® (amivantamab-vmjw) with standard care now approved in the U.S. as the sole targeted treatment reducing disease progression risk by over 50% for second-line EGFR-mutated advanced lung cancer.
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Edgewise Therapeutics Announces Positive Phase 1 and Phase 2 CIRRUS-HCM Study Results in Obstructive Hypertrophic Cardiomyopathy
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Edgewise Therapeutics Announces Positive Phase 1 and Phase 2 CIRRUS-HCM Study Results in Obstructive Hypertrophic Cardiomyopathy
24 September 2024
Edgewise Therapeutics Reports Favorable Results from Phase 1 Study in Healthy Volunteers and Phase 2 CIRRUS-HCM Study in Obstructive Hypertrophic Cardiomyopathy Patients.
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4DMT Highlights Promising Clinical Results for 4D-150 and Reveals Phase 3 Strategy at Wet AMD Program Event
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4DMT Highlights Promising Clinical Results for 4D-150 and Reveals Phase 3 Strategy at Wet AMD Program Event
24 September 2024
4DMT Showcases Strong and Lasting Clinical Outcomes for 4D-150 and Unveils 4FRONT Phase 3 Program Plan at 4D-150 Wet AMD Development Event.
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Promising Outcomes from Transcenta's Osemitamab Triple Trial in G/GEJ Cancer at ESMO 2024
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Promising Outcomes from Transcenta's Osemitamab Triple Trial in G/GEJ Cancer at ESMO 2024
24 September 2024
Transcenta Shares Promising Results from First-Line Triple Combination Trial of Osemitamab (TST001) for G/GEJ Cancer at ESMO 2024.
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Phase III trial results indicate Xofluza greatly lowers the spread of flu viruses
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Phase III trial results indicate Xofluza greatly lowers the spread of flu viruses
24 September 2024
Genentech revealed favorable topline results from the Phase III CENTERSTONE trial of Xofluza® (baloxavir marboxil).
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Satellos Reports Initial Participant Dosed in Phase 1 Clinical Trial of SAT-3247
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Satellos Reports Initial Participant Dosed in Phase 1 Clinical Trial of SAT-3247
19 September 2024
Satellos Bioscience announced that the initial participant has received a dose in a Phase 1 clinical trial of SAT-3247.
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