Jan 8 (Reuters) - CRISPR Therapeutics AG CRSP.BN :
* CRISPR THERAPEUTICS HIGHLIGHTS STRATEGIC PRIORITIES AND
2024
OUTLOOK
* FDA HAS ASSIGNED A PRESCRIPTION DRUG USER FEE ACT (PDUFA)
ACTION
DATE OF MARCH 30, 2024, FOR CASGEVY IN TDT
* ADDITIONAL REGULATORY SUBMISSIONS FOR CASGEVY ARE
CURRENTLY
UNDER REVIEW IN SWITZERLAND AND KINGDOM OF SAUDI ARABIA
* SUBMISSIONS FOR CASGEVY IN CANADA PLANNED FOR FIRST HALF
OF 2024
* CRISPR THERAPEUTICS PLANS TO INITIATE A CLINICAL TRIAL OF
CTX112
IN SYSTEMIC LUPUS ERYTHEMATOSUS (SLE) IN FIRST HALF OF 2024
* VIACYTE HAS ELECTED TO OPT-OUT OF COLLABORATION WITH CO
* PER OPT-OUT TERMS, COLLABORATION ASSETS WILL NOW BE WHOLLY
OWNED
BY CO, SUBJECT TO ROYALTY ON FUTURE SALES OWED TO VIACYTE
* OPT-OUT WILL BECOME EFFECTIVE IN EARLY FEBRUARY
* VERTEX CONTINUES TO HAVE NON-EXCLUSIVE RIGHTS TO CERTAIN
CRISPR
THERAPEUTICS' CRISPR/CAS9 TECHNOLOGY
Source text for Eikon: ID:nGNX8Q4cHT
Further company coverage: CRSP.BN
((Reuters.Briefs@thomsonreuters.com;))