
Clustered regularly interspaced short palindromic repeats (CRISPR)-based therapeutics are rapidly gaining traction for the management of infectious diseases. Programs targeting pathogens such as the human immunodeficiency virus (HIV), herpes simplex virus (HSV), and drug-resistant Escherichia coli (E. coli) are advancing in the clinic, signaling a transformative shift in the infectious disease space.
CRISPR-based therapeutics show potential to combat antimicrobial resistance (AMR) and deliver functional cures for chronic viral infections, says pharma analytics company GlobalData.
GlobalData’s latest report, “CRISPR Gene Editing in Infectious Diseases: Market Overview”, reveals that programmable gene editing technologies are now being investigated in clinical trials to address long-standing unmet needs in both viral and bacterial infections, with companies such as Excision BioTherapeutics, BDGene Therapeutics, Locus Biosciences and SNIPR Biome leading the charge.
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