Recent blog posts
AbbVie Reports Positive Phase 3 Results for Tavapadon in Solo Parkinson's Treatment
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AbbVie Reports Positive Phase 3 Results for Tavapadon in Solo Parkinson's Treatment
30 September 2024
AbbVie Reveals Promising Phase 3 TEMPO-1 Trial Results for Tavapadon as a Solo Parkinson’s Therapy.
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Merck to Present New Data on Anti-TL1A Monoclonal Antibody Tulisokibart (MK-7240) in IBD at UEG Week 2024
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Merck to Present New Data on Anti-TL1A Monoclonal Antibody Tulisokibart (MK-7240) in IBD at UEG Week 2024
30 September 2024
Merck to Showcase Extended Data on Tulisokibart (MK-7240), a Trial Anti-TL1A Monoclonal Antibody, in IBD at UEG Week 2024.
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Capstan Therapeutics to Present CPTX2309 Preclinical Results at 2024 ACR Convergence
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Capstan Therapeutics to Present CPTX2309 Preclinical Results at 2024 ACR Convergence
30 September 2024
Capstan Therapeutics will showcase preclinical findings on their lead in vivo CAR-T candidate, CPTX2309, at the 2024 ACR Convergence.
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Enanta Pharmaceuticals Announces Promising Phase 2a Results for EDP-323 in RSV-Challenged Healthy Adults
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Enanta Pharmaceuticals Announces Promising Phase 2a Results for EDP-323 in RSV-Challenged Healthy Adults
30 September 2024
Enanta Pharmaceuticals Reveals Encouraging Phase 2a Results for EDP-323 in Healthy Adults Challenged with RSV.
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Detalimogene Shows 71% Full Response Rate at Any Point in Early LEGEND Study Cohort Analysis
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Detalimogene Shows 71% Full Response Rate at Any Point in Early LEGEND Study Cohort Analysis
30 September 2024
enGene Holdings Advances in Clinical-Stage Genetic Medicine with Key Study on Non-Viral Therapy for High-Risk Bladder Cancer.
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Sage Therapeutics Ends Partnership with Biogen on SAGE-324 Project
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Sage Therapeutics Ends Partnership with Biogen on SAGE-324 Project
29 September 2024
Sage Therapeutics, Inc. (NASDAQ: Sage) disclosed that Biogen has relinquished its rights under the collaboration and license deal with Sage concerning the SAGE-324 program.
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LEO Pharma Presents Temtokibart and Dupilumab Phase 2a Results in Moderate-to-Severe Atopic Dermatitis at 2024 EADV Conference
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LEO Pharma Presents Temtokibart and Dupilumab Phase 2a Results in Moderate-to-Severe Atopic Dermatitis at 2024 EADV Conference
29 September 2024
LEO Pharma Unveils New Phase 2a Trial Findings for Temtokibart and Dupilumab in Moderate-to-Severe Atopic Dermatitis at 2024 EADV Annual Conference.
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ReCode Therapeutics Begins Phase 1b Trial of RCT2100 for Cystic Fibrosis Treatment
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ReCode Therapeutics Begins Phase 1b Trial of RCT2100 for Cystic Fibrosis Treatment
29 September 2024
ReCode Therapeutics Administers Initial Dose in Phase 1b Study of RCT2100 for Cystic Fibrosis Treatment.
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Tagrisso gains US approval for treating inoperable Stage III lung cancer with EGFR mutations
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Tagrisso gains US approval for treating inoperable Stage III lung cancer with EGFR mutations
29 September 2024
AstraZeneca’s Tagrisso (osimertinib) has received approval in the United States for treating adult patients with unresectable Stage III EGFRm NSCLC.
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FDA Approves First Liquid Form of Recombinant Botulinum Toxin Type A
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FDA Approves First Liquid Form of Recombinant Botulinum Toxin Type A
29 September 2024
The FDA has granted IND approval for the world's first liquid recombinant Botulinum Toxin Type A formulation.
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NMPA Approves Innovent's Picankibart for Moderate to Severe Plaque Psoriasis Treatment
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NMPA Approves Innovent's Picankibart for Moderate to Severe Plaque Psoriasis Treatment
29 September 2024
Innovent Reports NMPA NDA Approval for Picankibart (Anti-IL-23p19 Antibody) in Moderate to Severe Plaque Psoriasis Treatment.
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Pfizer Recalls Global Batches of Sickle Cell Drug OXBRYTA®
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Pfizer Recalls Global Batches of Sickle Cell Drug OXBRYTA®
29 September 2024
Pfizer Voluntarily Removes All Batches of Sickle Cell Disease Drug OXBRYTA® (voxelotor) From Global Market.
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