Recent blog posts
Promising Results for BTX-A51 in Liposarcoma Models: Edgewood Oncology's Trial Findings
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Promising Results for BTX-A51 in Liposarcoma Models: Edgewood Oncology's Trial Findings
8 April 2024
Edgewood Oncology reveals encouraging outcomes from a research-driven trial for BTX-A51 in early tests on liposarcoma models.
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Alnylam's KARDIA-2 Trial: Positive Zilebesiran Results in Uncontrolled Hypertension
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Alnylam's KARDIA-2 Trial: Positive Zilebesiran Results in Uncontrolled Hypertension
8 April 2024
Alnylam Unveils Encouraging Outcomes from Phase 2 KARDIA-2 Trial with Zilebesiran on Top of Usual Hypertension Medications in Subjects with Poorly Managed High Blood Pressure.
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Semi-Annual Leqvio® Boosts Statin Efficacy in Lowering Cholesterol in Real-World Care
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Semi-Annual Leqvio® Boosts Statin Efficacy in Lowering Cholesterol in Real-World Care
8 April 2024
Recent insights reveal that supplementing standard statin treatment with semi-annual doses of Leqvio® (inclisiran) can markedly decrease bad cholesterol levels in individuals with atherosclerotic cardiovascular disease in practical healthcare situations.
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Ocugen Announces Positive DSMB Review and Begins Recruiting for Mid-Dose OCU410 Trial in Early Geographic Atrophy Study
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Ocugen Announces Positive DSMB Review and Begins Recruiting for Mid-Dose OCU410 Trial in Early Geographic Atrophy Study
8 April 2024
Ocugen Reports Encouraging Results and DSMB Assessment, Launches Participant Recruitment for Intermediate Dosage Trial of OCU410, a Genetic Treatment Option, in Early-Stage ArMaDa Research Targeting Geographic Atrophy.
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Cidara Therapeutics Showcases New Findings on Innovative Drug-Fc Fusion Molecules at AACR's 2024 Meeting
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Cidara Therapeutics Showcases New Findings on Innovative Drug-Fc Fusion Molecules at AACR's 2024 Meeting
8 April 2024
Cidara Therapeutics uses its Cloudbreak technology to develop novel drug-Fc conjugates. The company will showcase four posters at the AACR Annual Meeting.
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Adcentrx to Present Early Nectin-4 ADC Data at 2024 AACR Convention
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Adcentrx to Present Early Nectin-4 ADC Data at 2024 AACR Convention
3 April 2024
Adcentrx Therapeutics will showcase early-stage findings of their Nectin-4 antibody-drug conjugate (ADC) initiative at the 2024 AACR Annual Convention.
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Carisma Therapeutics Offers Corporate Progress Report and Presents Q4 and Annual Financials for 2023
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Carisma Therapeutics Offers Corporate Progress Report and Presents Q4 and Annual Financials for 2023
3 April 2024
Carisma Therapeutics reported its Q4 financial results and year-end figures as of December 31, 2023, and provided a corporate update.
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FDA Approves VOYDEYA™ for Extravascular Hemolysis in PNH with Ravulizumab or Eculizumab
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FDA Approves VOYDEYA™ for Extravascular Hemolysis in PNH with Ravulizumab or Eculizumab
3 April 2024
The FDA has cleared VOYDEYA™ for use alongside ravulizumab or eculizumab in managing extravascular hemolysis among adult patients with the uncommon disorder PNH.
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Vertex Progresses VX-147 to Phase 3 Segment of Combined Phase 2/3 Study for APOL1-Related Kidney Conditions
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Vertex Progresses VX-147 to Phase 3 Segment of Combined Phase 2/3 Study for APOL1-Related Kidney Conditions
3 April 2024
Vertex Pharmaceuticals Incorporated revealed the progression of inaxaplin (VX-147) to the critical Phase 3 segment of the worldwide Phase 2/3 clinical study focusing on APOL1-related renal conditions.
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Asha Therapeutics Announces ASHA-624, a Novel Treatment Candidate for ALS
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Asha Therapeutics Announces ASHA-624, a Novel Treatment Candidate for ALS
3 April 2024
Asha Therapeutics has revealed its selection of an innovative internal-binding compound, designated ASHA-624, intended as a treatment agent to alter the progression of Amyotrophic Lateral Sclerosis.
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U.S. Review of Datopotamab Deruxtecan for Pre-Treated HR+/HER2- Breast Cancers
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U.S. Review of Datopotamab Deruxtecan for Pre-Treated HR+/HER2- Breast Cancers
3 April 2024
The U.S. authorities have endorsed the review of a licensing request for Datopotamab Deruxtecan.
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IASO Bio Reveals Chinese Regulatory Green Light for Advanced MM Therapy with Equecabtagene Autoleucel
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IASO Bio Reveals Chinese Regulatory Green Light for Advanced MM Therapy with Equecabtagene Autoleucel
3 April 2024
IASO Bio has disclosed official authorization from the China National Medical Products Administration for the clinical trial application of Equecabtagene Autoleucel.
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