Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
Narsoplimab by Omeros Demonstrates Improved Survival in TA-TMA Patients, Meets Key Trial Milestone
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Narsoplimab by Omeros Demonstrates Improved Survival in TA-TMA Patients, Meets Key Trial Milestone
25 December 2024
Omeros' Narsoplimab Achieves Key Trial Goal – Data Analysis Reveals Better Survival Compared to External Control in TA-TMA Patients.
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Favorable Phase 1b Results for Sorriso's SOR102 in Ulcerative Colitis Treatment
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Favorable Phase 1b Results for Sorriso's SOR102 in Ulcerative Colitis Treatment
25 December 2024
Sorriso Pharmaceuticals Reveals Favorable Phase 1b Trial Results for SOR102 in Treating Ulcerative Colitis.
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Targeting Nectin-4: The Rise of Enfortumab Vedotin in ADC Cancer Therapy
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7 min read
Targeting Nectin-4: The Rise of Enfortumab Vedotin in ADC Cancer Therapy
24 December 2024
In recent years, a molecular target called Nectin-4 has emerged as a rising star in the field of anti-cancer drug development.
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Accord Healthcare Gains Approval for IMULDOSA®, a Stelara® Biosimilar
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Accord Healthcare Gains Approval for IMULDOSA®, a Stelara® Biosimilar
20 December 2024
Accord Healthcare has received approval to market IMULDOSA®, a biosimilar of ustekinumab, which is similar to Stelara®.
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SpliceBio Gets FDA Clearance for SB-007 in Stargardt Disease Trials
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SpliceBio Gets FDA Clearance for SB-007 in Stargardt Disease Trials
20 December 2024
SpliceBio has received IND clearance from the U.S. FDA for SB-007, allowing the start of Phase 1/2 clinical trials in Stargardt Disease patients.
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Elevation Oncology Expands Pipeline with HER3-Targeting ADC EO-1022 for Solid Tumors
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Elevation Oncology Expands Pipeline with HER3-Targeting ADC EO-1022 for Solid Tumors
20 December 2024
Elevation Oncology broadens its pipeline with the introduction of EO-1022, a HER3 ADC aimed at treating solid tumors that express HER3.
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FDA Approves Neurocrine's CRENESSITY™ for Congenital Adrenal Hyperplasia
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FDA Approves Neurocrine's CRENESSITY™ for Congenital Adrenal Hyperplasia
20 December 2024
Neurocrine Biosciences has received FDA approval for CRENESSITY™ (crinecerfont), the first of its kind therapy for both children and adults suffering from classic congenital adrenal hyperplasia.
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FDA Approves UNLOXCYT™ (Cosibelimab-ipdl) by Checkpoint Therapeutics
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FDA Approves UNLOXCYT™ (Cosibelimab-ipdl) by Checkpoint Therapeutics
20 December 2024
Checkpoint Therapeutics reveals that the FDA has approved UNLOXCYT™ (cosibelimab-ipdl).
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Pfizer's IBRANCE® Boosts Progression-Free Survival in HR+/HER2+ Breast Cancer
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4 min read
Pfizer's IBRANCE® Boosts Progression-Free Survival in HR+/HER2+ Breast Cancer
20 December 2024
In the Phase 3 PATINA trial, Pfizer's IBRANCE® combined with standard treatments improved median progression-free survival by more than 15 months in patients.
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Corcept Reports Phase 2 Study Outcomes for Dazucorilant in ALS Patients
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Corcept Reports Phase 2 Study Outcomes for Dazucorilant in ALS Patients
20 December 2024
This study was a Phase 2 trial assessing two doses of its unique selective cortisol modulator, dazucorilant, in patients diagnosed with ALS.
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FDA Approves Galderma's Nemluvio® for Moderate to Severe Atopic Dermatitis
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FDA Approves Galderma's Nemluvio® for Moderate to Severe Atopic Dermatitis
20 December 2024
Galderma has obtained FDA approval in the U.S. for Nemluvio® (Nemolizumab) aimed at treating patients with moderate to severe atopic dermatitis.
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Chemical Modifications and Delivery Strategies of ASOs and siRNAs in Gene Therapy
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9 min read
Chemical Modifications and Delivery Strategies of ASOs and siRNAs in Gene Therapy
19 December 2024
Antisense oligonucleotides (ASOs) and small interfering RNAs (siRNAs), as vital components of precision medicine, have demonstrated tremendous potential in the field of gene therapy.
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