March 14 (Reuters) – Allergan said on Tuesday it would get exclusive access and the option to license up to five of Editas Medicine’s experimental gene-editing-based eye treatments under a research and development deal between the two companies.
The five eye programs include Editas’s lead drug, which is currently in pre-clinical development, to treat a rare, inherited eye disorder called Leber Congenital Amaurosis, the two companies said in a joint statement.
Editas’ gene-editing technology is called CRISPR and it is expected to revolutionize the treatment of genetic diseases. CRISPR works as a type of molecular scissors that can trim away unwanted pieces of genetic material, and replace them with new ones.
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