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DPRX

Dipexium Pharmaceuticals

16:44
12/22/16
12/22
16:44
12/22/16
16:44

Dipexium Pharmaceuticals and PLx Pharma announce merger agreement

Dipexium Pharmaceuticals and PLx Pharma, a privately held late-stage specialty pharmaceutical company, have entered into a definitive agreement under which PLx Pharma will merge with a wholly-owned subsidiary of Dipexium in an all-stock transaction. Following closing, Dipexium will be renamed PLx Pharma, and will operate under the leadership of the PLx management team with Michael Valentino serving as Executive Chairman of the board and Natasha Giordano serving as CEO. The combined company will initially be focused on completion of manufacturing scale-up and label finalization for the previously conditionally approved AspertecTM 325 mg aspirin dosage form thereby satisfying the open conditional items, and filing of a sNDA for Aspertec 81 mg maintenance dose form. Aspertec is being developed to provide high-risk cardiovascular and neurology patients with more reliable and predictable antiplatelet efficacy as compared to enteric coated aspirin while also reducing the adverse gastric events common in an acute setting. PLx stockholders will receive newly issued shares of common stock of Dipexium in connection with the merger contemplated by the merger agreement. Dipexium will issue approximately 36 million new shares of its common stock to PLx stockholders under the exchange ratio formula defined in the merger agreement. Upon the closing of the merger, existing PLx stockholders are expected to own 76.75% of Dipexium common shares outstanding and existing Dipexium stockholders are expected to own 23.25% of Dipexium common shares outstanding. The exchange ratio is defined in the merger agreement and is subject to potential adjustment. The merger is expected to close during 2Q17, subject to customary closing conditions.

DPRX Dipexium Pharmaceuticals

02/04/16
02/04/16
NO CHANGE

Dipexium Pharmaceuticals reaches 75% enrollment in Phase 3 trial of Locilex
Dipexium Pharmaceuticals' OneStep-1 and OneStep-2 pivotal Phase 3 clinical trials have reached the 75% enrollment milestone, in the aggregate, with each study having enrolled nearly the same number of patients. OneStep-1 and OneStep-2 are identical, pivotal Phase 3 clinical trials of 180 patients per clinical trial being conducted under a Special Protocol Assessment agreement between the FDA and Dipexium for evaluation of Locilex for the treatment of patients with mild infections of diabetic foot ulcers. The company anticipates completing these trials in 2H16 and is targeting an NDA submission with the FDA in 1H17 and a Marketing Authorization Application submission with the European Medicines Agency in 2H17.
10/25/16
FLTL
10/25/16
DOWNGRADE
FLTL
Hold
Dipexium Pharmaceuticals downgraded to Hold from Buy at Feltl
10/25/16
RAJA
10/25/16
DOWNGRADE
RAJA
Market Perform
Dipexium downgraded to Market Perform from Outperform at Raymond James

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