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June 2023 Global Innovative Drug Report 

Our newly published June 2023 Global Innovative Drug Report offers a comprehensive overview of the latest pharma advancements. It covers a detailed analysis of each selected drug, examining its active patents, mechanisms of action, associated clinical trials, competitive landscape, and more.

This report explores:

  1. The first approved drugs in June 
  1. New drug analysis 
  1. Global drugs under expedited review pathway in June 
  1. Analysis of selected ERP drugs 

Global Innovative Drug Report Summary

June 2023 Global Innovative Drug Report 

1.) First Approved Drugs in June 

June 2023 was a busy month for drug approvals, with 14 new drugs getting the green light. These new approvals include seven small molecule drugs (SMD), one monoclonal antibody (mAb), one enzyme, 1 CAR-T, one FcRN, one cell therapy, one micro-dystrophin, and one traditional Chinese medicine.

June 2023 Global Approved Drugs, Synapse
June 2023 Global Approved Drugs, Synapse 

2.) Comprehensive analysis of newly introduced medications 

This report also highlights five recently approved and provides an in-depth analysis of each. Here’s an example of the details can expect to uncover, using the example of Vorolanib:

Vorolanib Snapshot & R&D Status, Patsnap Synapse
Vorolanib Snapshot & R&D Status, Patsnap Synapse 
Vorolanib Active Patent & Analysis, Patsnap Synapse
Vorolanib Active Patent & Analysis, Patsnap Synapse 
Vorolanib Analysis Continued, Patsnap Synapse
Vorolanib Analysis Continued, Patsnap Synapse 

3.) Global Drugs under Expedited Review Pathway in June 

In June 2023, 58 drugs were under expedited review pathways. The designations include:

  • 32 orphan drugs
  • 12 fast track
  • 9 priority review
  • 4 breakthrough therapy
  • 2 accelerated approval
  • 1 qualified infectious disease product
  • 1 PRIME
June 2023 Global Drugs Subject to Expedited Review, Synapse
June 2023 Global Drugs Subject to Expedited Review, Synapse 

4.) Analysis of Selected ERP Drugs 

Our experts also selected six ERP drugs to analyze. Here’s an example of the information contained for each, using PRGN-12:

PRGN-2012 Snapshot & Active Patent, Patsnap Synapse
PRGN-2012 Snapshot & Active Patent, Patsnap Synapse 
PRGN-2012 Analysis, PatSnap Synapse
PRGN-2012 Analysis, PatSnap Synapse 

Gain Access to the Comprehensive Report for FREE – Download Now! If you aren’t registered for Synapse (registration is required to download the report), click here to register for free.

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Our platform is designed to accelerate the research process for pharmaceutical analysts by leveraging a wealth of connected data, including drug approvals, clinical trials, patents, non-patent literature, and news. With Synapse, users gain a comprehensive 360-degree view of the competitive and technological landscape, empowering them to make informed decisions quickly and efficiently. Discover the power of Synapse and revolutionize your research today.


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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