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Cell and Gene Therapies in CNS Disorders Research Report 2024: Pricing and Reimbursement Assessment, Current Treatment Options, Likelihood of Approval and Phase, Future Sales - Forecasts to 2029 - ResearchAndMarkets.com


The "Cell and Gene Therapies in CNS Disorders" report has been added to ResearchAndMarkets.com's offering.

The analyst anticipates that the global CGT market value in CNS disorders will experience significant growth - sales are expected to increase from $1.5 billion in 2023 to $12.2 billion in 2029, at a compound annual growth rate (CAGR) of 42.4%. Gene therapies will dominate the CGT market in CNS disorders. This is attributed to strong players such as Sarepta Therapeutics and Novartis with marketed products Elevidys and Zolgensma, respectively.

Overview of cell and gene therapies (CGT) in CNS Disorders. The report focuses on the marketed CGT assets addressing CNS disorders as well as the top five CNS indications with the most CGT pipeline assets. Clients will gain insight into the competitive landscape of leading CGT agents in CNS disorders including launch date projections, analyst consensus forecasts, likelihood of approval analysis, and commentary on current and future players.

The report also includes outlook from three key opinion leaders in the 5EU, US, and Japan, and analyses key challenges and opportunities in the application of CGTs in CNS disorders. Additionally, the report includes commentary on the regulatory landscape of CGTs and on the reimbursement environment.

Currently, there are eight cell and gene therapies (CGT) on the market for various central nervous system (CNS) disorders. This includes three gene therapies, two gene-modified cell therapies, and three conditionally approved cell therapies. Novartis's Zolgensma (onasemnogene abeparvovec) for the treatment of spinal muscular atrophy (SMA) was the first CGT asset to receive traditional approval in the CNS market in 2019.

Over the past five years, there has been an increase in the number of traditionally approved CGTs for genetic disorders such as metachromatic leukodystrophy (MLD), cerebral adrenoleukodystrophy (CALD), aromatic L-amino acid decarboxylase deficiency (AADCD), and Duchenne muscular dystrophy (DMD).

Reasons to Buy

A selection of companies mentioned in this report includes

Key Topics Covered:

1. Preface

2. Executive Summary

3. Current Treatment Options

4. Pricing and Reimbursement Assessment

5. Regulations

6. Future Market Assessment

7. Likelihood of Approval and Phase - Transition Success Rate Analysis

8. Sales Forecast

9. Appendix

For more information about this report visit https://www.researchandmarkets.com/r/r9zq42

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