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On October 25, 2017, NuLife Sciences Inc. (“NuLife”) entered into a non-binding term sheet (the “Term Sheet”) with Ensysce Biosciences, Inc. (“Ensysce”) regarding a proposed transaction (the “Transaction”) between the parties.

The Term Sheet contemplates a proposed acquisition of 100% of the outstanding capital stock of Ensysce by NuLife, or a subsidiary of NuLife. In consideration for the outstanding capital stock of Ensysce, at the closing of the proposed transaction, NuLife will issue such number of shares of its common stock to the Ensysce shareholders resulting in the Ensysce shareholders holding between 85% and 90% of the post-closing fully-diluted outstanding shares of NuLife’s common stock.

The Term Sheet is non-binding and closing of the Transaction is subject to satisfactory completion of due diligence by each party, negotiation and execution of definitive agreements, approval of the Transaction by the shareholders of each company, and satisfaction of financing requirements, among other conditions. There are no assurances that the parties will be successful in negotiating acceptable definitive agreements, or that the Transaction will be consummated on the terms described in the Term Sheet or at all.

Each party agrees to use commercially reasonable efforts to negotiate in good faith the terms of the Definitive Agreement and to execute the Definitive Agreement on or before November 30, 2017.

NuLife has agreed that, until November 30, 2017, except as otherwise approved in writing by Ensysce, NuLife will not entertain, solicit, or encourage any inquiry from any third party concerning any potential transaction that is inconsistent with the Transaction.

Ensysce, of San Diego, California, is a clinical state company with delivery platforms for both small and large molecule therapies. Ensysce's BIO-MD™ is a prodrug delivery platform that provides abuse deterrence to a long list of prescription drugs, including opioid products. The prodrugs are activated in a 2-step, enzyme mediated reaction only after oral administration. This process removes the patient's ability to abuse the drug by inhalation or through kitchen chemistry and intravenous injection. Ensysce has recently completed a Phase I trial with its lead oxycodone product, PF614. The trial showed over 90% efficient release of oxycodone and an improved safety profile over OxyContin™. Ensysce is also developing a delivery platform offering a novel approach for intravenous delivery of immunology and gene therapy products using single walled carbon nanotubes.