Pharmaceutical Insights
Navigate pharmaceutical trends with our insights on targets, institutional pipelines, clinical advances, and new drugs.
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Recent blog posts
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
Latest Hotspot
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
Latest Hotspot
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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How to check the compliance of subjects?
Knowledge Base
3 min read
How to check the compliance of subjects?
16 January 2024
The drug packaging box sent to the subject will be returned to the investigator by the subject after the end of the trial.
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Corbus Pharma Secures US FDA Approval for Phase 1 Trial of its Novel αvβ8 Antibody, CRB-601
Latest Hotspot
3 min read
Corbus Pharma Secures US FDA Approval for Phase 1 Trial of its Novel αvβ8 Antibody, CRB-601
16 January 2024
Corbus Pharmaceuticals Holdings, Inc., focused on precision oncology, announced FDA approval for its CRB-601 drug application.
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Exploring the Latest PD-L1/SIRPα Bispecific Antibody Deal by Elpiscience Biopharma: A Guide to Rapidly Accessing Transaction Insights
DrugDeal Decode
5 min read
Exploring the Latest PD-L1/SIRPα Bispecific Antibody Deal by Elpiscience Biopharma: A Guide to Rapidly Accessing Transaction Insights
16 January 2024
Elpiscience Biopharma and Astellas Pharma have teamed up in a deal for the BiME® platform, advancing two drugs, ES019 and a second molecular project.
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Constant Therapeutics Reveals Initial Participant Receives Treatment in Stage 2 Study for Stroke Rehab using Drug TXA127
Latest Hotspot
3 min read
Constant Therapeutics Reveals Initial Participant Receives Treatment in Stage 2 Study for Stroke Rehab using Drug TXA127
16 January 2024
Constant Therapeutics LLC, specializing in biopharmaceuticals, announced the first patient dosed in their Phase 2 trial of TXA127, a peptide therapy aimed at improving post-stroke recovery.
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Expand your analysis with a 360° industry overview!
Bio Sequence
3 min read
Expand your analysis with a 360° industry overview!
16 January 2024
Gain instant access to industry insights for your sequence of interest, with exportable reports summarizing length and identity distribution, drug and patent activity, IP and literature trends, and more!
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FDA Fast-Tracks Review of Supplements to TIVDAK® License for Those Suffering from Advanced Cervical Cancer Relapse or Spread
Latest Hotspot
3 min read
FDA Fast-Tracks Review of Supplements to TIVDAK® License for Those Suffering from Advanced Cervical Cancer Relapse or Spread
15 January 2024
Pfizer and Genmab announced the FDA has accepted their supplemental application for TIVDAK.
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