Clinical Trials Portfolio and Regulatory History of Idelalisib in Indolent Non-Hodgkin Lymphoma: A Systematic Review and Meta-analysis.

Author: BanerjeeTitas, HaslamAlyson, KimMyung Sun, PrasadVinay

Paper Details 
Original Abstract of the Article :
Idelalisib is a first-in-class phosphatidylinositol 3-kinase inhibitor that received US Food and Drug Administration accelerated approval in July 2014 as a single-agent treatment for relapsed follicular lymphoma (FL) and small lymphocytic lymphoma (SLL). Serious adverse effects were reported in 2016...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028543/

データ提供:米国国立医学図書館(NLM)

The Rise and Fall of Idelalisib: A Journey Through Clinical Trials and Regulatory Decisions

This systematic review and meta-analysis traces the journey of idelalisib, a first-in-class phosphatidylinositol 3-kinase inhibitor, through clinical trials and regulatory processes. The authors examine the drug's development, approval, and eventual withdrawal from the market. The review delves into the clinical trials portfolio and regulatory history of idelalisib, highlighting the challenges and complexities of drug development and approval.

A Tale of Two Approvals

The review highlights the complexities of drug development and regulatory processes. Idelalisib initially received accelerated approval for treating relapsed follicular lymphoma and small lymphocytic lymphoma. However, serious adverse effects and subsequent termination of postmarketing registry trials led to the drug's eventual withdrawal from the market. This case study demonstrates the importance of ongoing monitoring and evaluation of drug safety and efficacy, even after initial approval.

Navigating the Shifting Sands of Drug Development

This review emphasizes the unpredictable nature of drug development. It's like traversing a vast desert, where the landscape constantly shifts with new findings and challenges. The study highlights the importance of careful consideration of both efficacy and safety, and the need for a comprehensive approach to drug development and evaluation.

Dr.Camel's Conclusion

This review provides a valuable case study of the challenges and complexities of drug development and regulatory processes. It underscores the importance of ongoing monitoring and evaluation, and the need for a comprehensive approach to drug safety and efficacy assessment. While idelalisib's journey ultimately ended in withdrawal, it serves as a reminder of the importance of continuous learning and adaptation in the field of drug development.

Date :
  1. Date Completed 2023-05-03
  2. Date Revised 2023-05-25
Further Info :

Pubmed ID

36939665

DOI: Digital Object Identifier

PMC10028543

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Languages

English

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