Flexion Therapeutics, Inc. (NASDAQ:FLXN) Files An 8-K Regulation FD Disclosure

0

Flexion Therapeutics, Inc. (NASDAQ:FLXN) Files An 8-K Regulation FD Disclosure
Item 7.01Regulation FD Disclosure.

On July10, 2017, Flexion Therapeutics, Inc. issued a press release noting topics to be presented at its investor and analyst day event, including information with respect to its new FX101 Fluticasone ER development program. A copy of the press release is attached hereto as Exhibits 99.1 and incorporated by reference herein.

Item 9.01Financial Statements and Exhibits.

Exhibit No.

Description

99.1 Press Release of Flexion Therapeutics, Inc. dated July 10, 2017.


Flexion Therapeutics Inc Exhibit
EX-99.1 2 d423100dex991.htm EX-99.1 EX-99.1 Exhibit 99.1   Flexion Therapeutics to Hold Investor & Analyst Day Today –     Management to discuss the latest plans for the potential launch of ZilrettaTM –     Clinical experts to share perspectives on Zilretta –     Company to introduce new pipeline candidate (FX101) BURLINGTON,…
To view the full exhibit click here

About Flexion Therapeutics, Inc. (NASDAQ:FLXN)

Flexion Therapeutics, Inc. is a United States-based specialty pharmaceutical company. The Company is focused on the development and commercialization of local therapies for the treatment of patients with musculoskeletal conditions, beginning with osteoarthritis (OA), a type of degenerative arthritis. The Company’s lead product candidate, Zilretta, is a late-stage, injectable, extended-release, intra-articular (IA) investigational steroid. The Company is developing Zilretta as a treatment for patients with moderate to severe OA knee pain. The Company has specifically designed Zilretta to combine a steroid, triamcinolone acetonide (TCA) with poly lactic-co-glycolic acid (PLGA), for providing sustained therapeutic concentrations in the joint and persistent analgesic effect. The Company’s other product candidates include FX007 for post-operative pain and FX005 for the treatment of end-stage OA patients. The Company is engaged in conducting a Phase IIb clinical trial of Zilretta.