180 Life Sciences (NASDAQ: ATNF) is a clinical-stage biotechnology company focused on the development of novel drugs that fulfill unmet needs in inflammatory diseases, fibrosis and pain. The company today announced that it has submitted a request to the United Kingdom’s Medicines and Healthcare products Regulatory Agency (“MHRA”) for a follow-up scientific advice meeting where the company will seek guidance on a plan to obtain Conditional Marketing Authorization (“CMA”) for the use of adalimumab in the treatment of early stage Dupuytren’s disease. The meeting is anticipated to take place in the late third quarter, with written responses anticipated to be received prior to year-end 2023. According to the company’s regulatory consultants, an additional clinical trial (phase 3) may be required to obtain CMA approval, and such a trial has been designed. ATNF’s regulatory consultants believe obtaining of a CMA may be possible due to the long safety history of anti-tumor necrosis factor (“TNF”) therapies, conditional on a successful phase 3 trial, which, upon patient enrollment, the CMA may be granted prior to completion and based on the company’s commitment to complete the phase 3 trial.

To view the full press release, visit https://ibn.fm/tEnly

About 180 Life Sciences Corp.

180 Life Sciences is a clinical stage biotechnology company focused on the development of therapeutics for unmet medical needs in chronic pain, inflammation and fibrosis by employing innovative research, and, where appropriate, combination therapy. The company’s current primary focus is a novel program to treat several inflammatory disorders using anti-TNF (tumor necrosis factor).

NOTE TO INVESTORS: The latest news and updates relating to ATNF are available in the company’s newsroom at http://ibn.fm/ATNF

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