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Crestone Releases Encouraging Phase 2 Trial Results for CRS3123 in Treating C. Difficile Infections (CDI)
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Crestone Releases Encouraging Phase 2 Trial Results for CRS3123 in Treating C. Difficile Infections (CDI)
9 September 2024
Crestone, Inc. ("Crestone") announced promising initial results from its Phase 2 clinical trial of CRS3123 in patients with Clostridioides difficile infection (CDI).
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Aurinia Reports Initial Participant Dosed in AUR200 Single-Dose Trial
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Aurinia Reports Initial Participant Dosed in AUR200 Single-Dose Trial
9 September 2024
Aurinia Pharmaceuticals recently disclosed that the first participant has received the initial dose in a Phase 1a single ascending dose (SAD) clinical trial for AUR200.
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Fenebrutinib by Roche Significantly Reduces Disease Activity and Disability Progression in Relapsing Multiple Sclerosis Over 48 Weeks
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Fenebrutinib by Roche Significantly Reduces Disease Activity and Disability Progression in Relapsing Multiple Sclerosis Over 48 Weeks
9 September 2024
Roche's fenebrutinib showed almost total reduction in disease activity and disability advancement for as long as 48 weeks in patients with relapsing multiple sclerosis.
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Invivyd Initiates Phase 1 Trial of New COVID-19 Monoclonal Antibody VYD2311, Building on PEMGARDA™ Success
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Invivyd Initiates Phase 1 Trial of New COVID-19 Monoclonal Antibody VYD2311, Building on PEMGARDA™ Success
9 September 2024
Invivyd starts initial dosing in Phase 1 trial of VYD2311, a new monoclonal antibody for COVID-19, expanding on PEMGARDA™'s success.
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Biogen Announces Promising Results for Higher-Dose Nusinersen in SMA Therapy
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Biogen Announces Promising Results for Higher-Dose Nusinersen in SMA Therapy
9 September 2024
Biogen Reports Encouraging Topline Results from Study on Higher Dose of Nusinersen, Demonstrating Notable Success in SMA Treatment.
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OncoC4 Initiates Phase 1 Trial of SIGLEC10 Inhibitor ONC-841 for Solid Tumors
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OncoC4 Initiates Phase 1 Trial of SIGLEC10 Inhibitor ONC-841 for Solid Tumors
6 September 2024
OncoC4 Starts Phase 1 Trial Dosing First Patient with the New SIGLEC10 Checkpoint Inhibitor ONC-841 for Solid Tumors.
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Allyx Therapeutics Reports Initial Parkinson’s Patient Treated with ALX-001
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Allyx Therapeutics Reports Initial Parkinson’s Patient Treated with ALX-001
6 September 2024
Allyx Therapeutics has begun a new clinical trial for its key drug, ALX-001, administering it to the first patient to assess safety, pharmacokinetics, and potential therapeutic effects in Parkinson’s disease.
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Merck and EyeBio Initiate Phase 2b/3 Trial for Restoret™ in Diabetic Macular Edema Treatment
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Merck and EyeBio Initiate Phase 2b/3 Trial for Restoret™ in Diabetic Macular Edema Treatment
6 September 2024
Merck and EyeBio Announce Start of Phase 2b/3 Clinical Study for Restoret™ to Treat Diabetic Macular Edema.
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FDA Approves BlueRock Therapeutics' IND for iPSC-Derived Cell Therapy OpCT-001 Targeting Photoreceptor Diseases
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FDA Approves BlueRock Therapeutics' IND for iPSC-Derived Cell Therapy OpCT-001 Targeting Photoreceptor Diseases
6 September 2024
BlueRock Therapeutics has obtained FDA approval for their IND application for OpCT-001, a cell therapy derived from iPSCs, targeting primary photoreceptor diseases.
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Vasa Therapeutics Initiates Phase 1 Trial of VS-041 for Heart Failure Treatment
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Vasa Therapeutics Initiates Phase 1 Trial of VS-041 for Heart Failure Treatment
6 September 2024
Vasa Therapeutics Begins Phase 1 Human Trial of VS-041 for Treating Heart Failure with Preserved Ejection Fraction.
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GC Biopharma and Hanmi Pharmaceutical get U.S. FDA IND approval for Phase 1/2 trial
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GC Biopharma and Hanmi Pharmaceutical get U.S. FDA IND approval for Phase 1/2 trial
6 September 2024
GC Biopharma revealed that its joint effort with Hanmi Pharmaceutical on the Fabry treatment 'LA-GLA' (GC1134A/HM15421) has been granted IND approval by the U.S. FDA to initiate a Phase 1/2 clinical study.
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REGENXBIO Reports Positive Results for RGX-121, Showing Lasting Systemic Impact
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REGENXBIO Reports Positive Results for RGX-121, Showing Lasting Systemic Impact
6 September 2024
REGENXBIO Inc. revealed encouraging findings from the Phase I/II/III CAMPSIITE® study of RGX-121, aimed at treating Mucopolysaccharidosis Type II (MPS II).
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