Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
What is a placebo in clinical trials?
"What" Series
2 min read
What is a placebo in clinical trials?
17 January 2024
In clinical trials, a placebo is an inactive substance or other intervention that looks the same and tastes the same as the active drug being tested.
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EyePoint Pharma announces first patient treatment in early-phase VERONA trial for EYP-1901 in diabetic eye swelling
Latest Hotspot
3 min read
EyePoint Pharma announces first patient treatment in early-phase VERONA trial for EYP-1901 in diabetic eye swelling
17 January 2024
EyePoint Pharma reports initial participant receives treatment in early-stage VERONA study assessing EYP-1901 for diabetic eye swelling.
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What is a sham in clinical trials?
"What" Series
2 min read
What is a sham in clinical trials?
17 January 2024
In clinical trials, a sham is a procedure or device that looks the same and feels the same as an active treatment being tested but doesn’t actually do anything.
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Ariceum Therapeutics has applied for a UK Clinical Trial Authorization to start testing its new Iodine-123 labeled PARP inhibitor in recurrent glioblastoma patients
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3 min read
Ariceum Therapeutics has applied for a UK Clinical Trial Authorization to start testing its new Iodine-123 labeled PARP inhibitor in recurrent glioblastoma patients
17 January 2024
Ariceum Therapeutics has submitted an application for a Clinical Trial Authorization (CTA) in the UK to conduct initial trials of its novel Iodine-123 tagged PARP inhibitor, targeting recurrent glioblastoma patients.
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What's clinical adverse event and it's classification?
"What" Series
2 min read
What's clinical adverse event and it's classification?
17 January 2024
Clinical adverse events (AEs) are any unintended or harmful signs, symptoms, or conditions linked in time to the use of a medical product, regardless of causality.
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EU Sanctions KRAZATI (adagrasib) as a Selective Therapy for Advanced NSCLC Sufferers Exhibiting KRAS G12C Alteration
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3 min read
EU Sanctions KRAZATI (adagrasib) as a Selective Therapy for Advanced NSCLC Sufferers Exhibiting KRAS G12C Alteration
16 January 2024
Mirati Therapeutics, Inc. announced today that the European Commission has granted conditional approval for their medication, KRAZATI® (adagrasib).
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Exploring the Latest TSLP monoclonal antibody Deal by Aiolos Bio: A Guide to Rapidly Accessing Transaction Insights
DrugDeal Decode
4 min read
Exploring the Latest TSLP monoclonal antibody Deal by Aiolos Bio: A Guide to Rapidly Accessing Transaction Insights
16 January 2024
GSK Plc agreed to buy Aiolos Bio, Inc. for $1 billion, plus up to $400 million in milestones, gaining access to Aiolos’s leading candidate, AIO-001, a long-acting anti-TSLP monoclonal antibody.
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Xeris Biopharma Secures Global Exclusive Rights to Distribute Xeriject® Version of Teprotumumab
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3 min read
Xeris Biopharma Secures Global Exclusive Rights to Distribute Xeriject® Version of Teprotumumab
16 January 2024
Xeris Biopharma has announced a global licensing agreement with Amgen for a subcutaneous teprotumumab injection using its XeriJect® system for Thyroid Eye Disease.
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What is IUPAC?
"What" Series
2 min read
What is IUPAC?
16 January 2024
The International Union of Pure and Applied Chemistry (IUPAC) is a non-governmental organization dedicated to promoting chemistry-related activities.
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STADA and Alvotech obtain green light for Uzpruvo, the inaugural European biosimilar to Stelara, based on ustekinumab
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3 min read
STADA and Alvotech obtain green light for Uzpruvo, the inaugural European biosimilar to Stelara, based on ustekinumab
16 January 2024
The European Commission has approved STADA and Alvotech's biosimilar Uzpruvo® (AVT04), similar to Stelara® (ustekinumab), for marketing.
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Exploring the Latest PROTACs Deal by Kymera Therapeutics: A Guide to Rapidly Accessing Transaction Insights
DrugDeal Decode
4 min read
Exploring the Latest PROTACs Deal by Kymera Therapeutics: A Guide to Rapidly Accessing Transaction Insights
16 January 2024
Kymera Therapeutics began their Phase 2 ADVANTA study for KT-474 in AD on Dec 7, 2023, prompting a $15M milestone payment from Sanofi.
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Verge Genomics has launched a preliminary study for VRG50635 as a potential ALS therapy
Latest Hotspot
3 min read
Verge Genomics has launched a preliminary study for VRG50635 as a potential ALS therapy
16 January 2024
Verge Genomics has announced the start of its Phase 1b trial for VRG50635, a potential treatment for amyotrophic lateral sclerosis (ALS), covering both sporadic and familial forms.
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