Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Is Adstiladrin approved by the FDA?
Drug Insights
3 min read
Is Adstiladrin approved by the FDA?
30 July 2024
Adstiladrin received FDA approval on December 16, 2022. It represents a significant advancement in cancer therapy, particularly for patients who have not responded to standard treatments.
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Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Jul 26
Pharma Frontiers
11 min read
Pharma Frontiers: Daily Digest of Global Pharmaceutical News – Jul 26
26 July 2024
Jul 26th latest updates in the global new drug development field, including progress in new drug research and development, transaction information, and partnership developments.
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Is Adagrasib approved by the FDA?
Drug Insights
4 min read
Is Adagrasib approved by the FDA?
26 July 2024
Adagrasib, marketed under the brand name Krazati, is an oral medication used to treat adults with non-small cell lung cancer (NSCLC).
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Promising Phase 2 Results for OSE Immunotherapeutics' Lusvertikimab in Treating Ulcerative Colitis
Latest Hotspot
3 min read
Promising Phase 2 Results for OSE Immunotherapeutics' Lusvertikimab in Treating Ulcerative Colitis
26 July 2024
OSE Immunotherapeutics Reports Promising Phase 2 Trial Outcomes for Lusvertikimab in Ulcerative Colitis Treatment.
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Is Olutasidenib approved by the FDA?
Drug Insights
3 min read
Is Olutasidenib approved by the FDA?
26 July 2024
Olutasidenib received FDA approval on December 1, 2022. This drug belongs to the class of miscellaneous antineoplastics.
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IASO Bio Gains U.S. FDA Green Light for Equecabtagene Autoleucel IND Application in Multiple Sclerosis
Latest Hotspot
3 min read
IASO Bio Gains U.S. FDA Green Light for Equecabtagene Autoleucel IND Application in Multiple Sclerosis
25 July 2024
IASO Biotechnology announced that the FDA has approved its application for a new drug, Equecabtagene Autoleucel (Eque-cel), a fully human anti-BCMA CAR T cell therapy.
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Is Rebyota approved by the FDA?
Drug Insights
2 min read
Is Rebyota approved by the FDA?
25 July 2024
Rebyota, a fecal microbiota product, is used to prevent the recurrence of Clostridioides difficile infection (CDI).
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Enterprise Therapeutics administers ETD001 to first cystic fibrosis patient in Phase 2 study
Latest Hotspot
4 min read
Enterprise Therapeutics administers ETD001 to first cystic fibrosis patient in Phase 2 study
25 July 2024
Enterprise Therapeutics has today revealed that the first participant with cystic fibrosis has been administered a dose in its Phase 2a study of ETD001.
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Is Etranacogene dezaparvovec approved by the FDA?
Drug Insights
3 min read
Is Etranacogene dezaparvovec approved by the FDA?
25 July 2024
Etranacogene dezaparvovec, marketed under the brand name Hemgenix, is a gene therapy used to treat adults with Hemophilia B.
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Merck Unveils Early Results for RSV Antibody Clesrovimab in Infants
Latest Hotspot
3 min read
Merck Unveils Early Results for RSV Antibody Clesrovimab in Infants
25 July 2024
Merck Reveals Preliminary Findings from Phase 2b/3 Study of Clesrovimab (MK-1654), an Experimental Monoclonal Antibody for RSV Prevention in Infants.
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Is Teplizumab approved by the FDA?
Drug Insights
4 min read
Is Teplizumab approved by the FDA?
25 July 2024
Teplizumab, marketed under the brand name Tzield, was approved by the FDA on November 17, 2022.
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FDA Approves Samsung Bioepis' EPYSQLI® as Soliris Biosimilar
Latest Hotspot
3 min read
FDA Approves Samsung Bioepis' EPYSQLI® as Soliris Biosimilar
25 July 2024
FDA Greenlights Samsung Bioepis' EPYSQLI® (eculizumab-aagh) as a Biosimilar to Soliris (eculizumab).
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