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180 life sciences (nasdaq: atnf)
today announced its engagement of Kinexum, a strategic advisory firm, to support the company in submitting a Marketing Authorisation Application (“MAA”) for adalimumab to treat progressive early-stage Dupuytren's disease. According to the announcement, the MAA will be submitted to the United Kingdom's Medicines and Healthcare products Regulatory Agency (“MHRA” or“Agency”). As part of the application, 180 Life Sciences expects to request a Conditional Marketing Authorisation (“CMA”), which assures the agency that long term outcome data will be forthcoming. Including costs associated with the Kinexum agreement, the company anticipates that it will spend approximately $900,000 to $1,000,000 in the next three quarters for activities associated with the MHRA filing and other regulatory preparations.
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About 180 Life Sciences Corp.
180 Life Sciences is a clinical-stage biotechnology company driving groundbreaking studies into clinical programs, which are seeking to address major unmet medical needs. The company's focus is a novel program to treat several inflammatory disorders using anti-TNF (tumor necrosis factor).
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