July 2023 Global Innovative Drug Report
Leveraging insights from our AI-powered life sciences intelligence platform Synapse, we’re delighted to present our July 2023 Global Innovative Drug Report.
This report offers a comprehensive overview of the latest advancements in the pharmaceutical industry and an analysis of each selected drug. It provides a snapshot of each drug and explores its R&D status, active patents, mechanisms of action, clinical trials, competitive landscape, and other pertinent factors.
The report consists of four parts:
- First Approved Drugs in July
- New Drug Analysis
- Global Drugs under Expedited Review Pathway in July
- Analysis of Selected ERP Drugs
Global Innovative Drug Report Overview
1.) First Approved Drugs in July
In July 2023, four drugs received global approval: a prophylactic vaccine, a small molecule drug (SMD), a monoclonal antibody, and a herbal medicine.
![Patsnap Synapse Global Approved Drugs July Anthrax Vaccine Lotilaner](png/july-2023-global-approved-drugs%e2%80%afsynapse-1024x661.png)
2.) New Drug Analysis
This report highlights two recently approved drugs, with a spotlight on CYFENDUS.
![Patsnap Synapse New Drug Analysis Anthrax Vaccine Adsorbed CYFENDUS](png/cyfendus-snapshot-analysis%e2%80%afpatsnap-synapse-724x1024.png)
![Patsnap Synapse CYFENDUS Mechanism, Application, Clinical Trials](png/cyfendus-analysis-continued%e2%80%afpatsnap-synapse-699x1024.png)
![Patsnap Synapse CYFENDUS Analysis to BioThrax](png/cyfendus-analysis-continued%e2%80%afpatsnap-synapse-2-734x1024.png)
3.) Global Drugs Under Expedited Review Pathway in July
In July 2023, a total of 41 drugs globally were on Expedited Review tracks. This includes 19 with Orphan Drug designations, eight designated as Breakthrough Therapies, seven on the Fast Track, four under Priority Review, two with Conditional Marketing Approvals, two targeting Rare Pediatric Diseases, and one as a Qualified Infectious Disease Product.
![July 2023 Global Drugs Subject to Expedited Review, Synapse](png/july-2023-global-drugs-subject-to-expedited-review%e2%80%afsynapse--829x1024.png)
4.) Analysis of Selected ERP Drugs
In this report, we’ve chosen to analyze seven drugs from the Expedited Review Pathway. Specifically, for Zenocutuzumab, the report explores the following aspects:
![Zenocutuzumab Snapshot & R&D Status & Active Patent, Patsnap Synapse](png/zenocutuzumab-snapshot-rd-status-active-patent%e2%80%afpatsnap-synapse-714x1024.png)
![Zenocutuzumab Analysis, PatSnap Synapse](png/zenocutuzumab-analysis%e2%80%afpatsnap-synapse-752x1024.png)
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Copyright Statement: This report is the sole property of Patsnap and is protected under copyright laws. Any reproduction, excerpting, or other use of this report without explicit authorization from Patsnap is strictly prohibited. Authorized products must be used within the scope of authorization and must include a clear indication of the source. Patsnap reserves the right to investigate any violations of this statement and pursue legal action as necessary. For inquiries regarding authorization, please contact [email protected].
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