Believed to be one of the great biotechnology breakthroughs, Gene Editing Market report is a powerful tool in pharmaceutical research that could radically change how certain diseases are treated. The precision and rapid-acting fashion of tools such as zinc-finger nucleases, transcription activator-like effector nucleases, and clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated protein 9 (Cas9) create untapped opportunity. But gene editing does not come without challenges and controversy, especially when it comes to safety and ethical issues.
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Key academic research performed over the past 20 years has led to important discoveries in CRISPR/Cas9 technology, and has also prompted a fierce intellectual property battle over which organization owns the foundational patents. Nevertheless, out of that research has come a wave of start-up companies that are inching toward commercial clinical development with gene editing therapy candidates. Along the way, these biotechs have secured partners, including large pharmaceutical companies, to advance development and eventually commercialization.
This report provides comprehensive analysis of:
Key market segments and sub-segments
Evolving market trends and dynamics
Changing supply and demand scenarios
Quantifying market opportunities through market sizing and market forecasting
Tracking current trends/opportunities/challenges
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Major TOC of Gene Editing Market:
Gene editing technologies evolve and improve over time
Multiple researchers have contributed to key academic discoveries in CRISPR/Cas9
The dispute over foundational CRISPR/Cas9 patents carries on
Many challenges and controversies remain in advancing CRISPR/Cas9 technology
Many players, from small biotechs to Big Pharma, are developing gene editing drug candidates
The gene editing pipeline is a small proportion of regenerative medicine therapies, and is dominated by CRISPR/Cas9
EVOLUTION OF GENE EDITING TECHNOLOGY
Gene editing can radically change how diseases are targeted
Gene editing is an emerging modality within the broader regenerative medicine market
Transcription activator-like effector nucleases
ORIGINS OF ACADEMIC RESEARCH IN CRISPR/CAS9
Academic research over the last 20 years has helped to advance CRISPR/Cas9 technology toward human therapeutic use
Many start-ups have been borne out of CRISPR/Cas9 academic research
CRISPR/CAS9 PATENT LITIGATION
Select key patent filings, issuances, and decisions
Patent pools and cross-licensing may help commercial drug developers avoid intellectual property barriers in the future
CHALLENGES AND CONTROVERSIES WITH GENE EDITING
Process challenges exist for gene editing tools
Editing human embryos pose ethical concerns
Safety issues plague gene editing
As is the case with many regenerative medicines, cost of gene editing therapies may be prohibitive
KEY COMPANIES IN GENE EDITING
Key players in gene editing span both biotech and large pharma companies
Profiles of select key gene editing companies
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