SORRENTO THERAPEUTICS, INC. (NASDAQ:SRNE) Files An 8-K Regulation FD Disclosure

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SORRENTO THERAPEUTICS, INC. (NASDAQ:SRNE) Files An 8-K Regulation FD Disclosure
Item 7.01. Regulation FD Disclosure.

On November 14, 2017, Sorrento Therapeutics, Inc. (the “Company”) issued a press release announcing that Scilex Pharmaceuticals Inc., a majority-owned subsidiary of the Company, has filed the European Marketing Authorization Application for its lead product candidate, ZTlidoTM (lidocaine medicated plaster 1.8%), through a hybrid regulatory pathway with the Medicines and Healthcare products Regulatory Agency in the United Kingdom. A copy of the press release is furnished herewith as Exhibit 99.1 to this Current Report on Form 8-K.

The information contained in this Item 7.01 and Exhibit 99.1 furnished as part of Item 9.01 of this Current Report on Form 8-K is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any registration statement or other filing under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference to such filing.

Item 9.01. Financial Statements and Exhibits.
99.1 Press release dated November 14, 2017.


Sorrento Therapeutics, Inc. Exhibit
EX-99.1 2 tv479455_ex99-1.htm EXHIBIT 99.1   Exhibit 99.1     FOR IMMEDIATE RELEASE     SCILEX PHARMACEUTICALS,…
To view the full exhibit click here

About SORRENTO THERAPEUTICS, INC. (NASDAQ:SRNE)

Sorrento Therapeutics, Inc. is a biopharmaceutical company. The Company is engaged in the discovery, acquisition, development and commercialization of drug therapeutics. Its primary therapeutic focus is oncology, including the treatment of chronic cancer pain. It is also developing therapeutic products for other indications, including immunology and infectious diseases. Its products in the pipeline include Chimeric Antigen Receptor-T Cell (CAR-T) programs, resiniferatoxin (RTX), and biosimilar/biobetter antibodies clinical development programs. Its pipeline also includes preclinical fully human therapeutic monoclonal antibodies (mAbs), including biosimilars/biobetters, fully human anti-PD-L1 and anti-PD-1 checkpoint inhibitors derived from its G-MAB library platform, antibody drug conjugates (ADCs), bispecific antibodies (BsAbs), as well as CAR-T and Chimeric Antigen Receptor Natural Killer (NK) cells (CAR. NK) for adoptive cellular immunotherapy.

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