LIPOCINE INC. (NASDAQ:LPCN) Files An 8-K Other Events
Item 8.01 Other Events
On December 20, 2018, Lipocine Inc. issued a press release announcing the presentation of LPCN 1144 clinical data at Keystone Symposia on Integrated Pathways of Disease in NASH and NAFLD in Santa Fe, New Mexico on January 22, 2019. The press release is filed as Exhibit 99.1 and are incorporated herein by reference.
Additionally, the Company will highlight the association of hypogonadism and non-alcoholic fatty liver disease (“NAFLD”) including LPCN 1144 clinical results in which liver fat was assessed via Magnetic Resonance Imaging-Proton Density Fat Fraction (“MRI-PDFF”) in hypogonadal males at the Keystone Symposia on Integrated Pathways of Disease in NASH and NAFLD. The abstract is filed as Exhibit 99.2.
Item 8.01 Financial Statements and Exhibits.
(d)Exhibits
The following exhibits are filed with this report:
Lipocine Inc. Exhibit
EX-99.1 2 tv509532_ex99-1.htm EXHIBIT 99.1 Exhibit 99.1 Lipocine Announces LPCN 1144 MRI-PDFF Clinical Results Selected for Presentation at Keystone Symposia on Integrated Pathways of Disease in NASH and NAFLD SALT LAKE CITY,…
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About LIPOCINE INC. (NASDAQ:LPCN)
Lipocine Inc. is a specialty pharmaceutical company. The Company is focused on applying its oral drug delivery technology for the development of pharmaceutical products in the area of men’s and women’s health. Its primary development programs are based on oral delivery solutions for bioavailable drugs. Its lead product candidate, LPCN 1021, is an oral testosterone replacement therapy (TRT), designed for twice-a-day dosing and is in Phase III testing. The Company’s additional pipeline candidates include LPCN 1111, an oral testosterone therapy product targeted for once daily dosing, which is in Phase II testing, and LPCN 1107, an oral therapy for the prevention of preterm birth, which is in Phase I testing. These products are based on its Lip’ral promicellar drug delivery technology platform. Lip’ral promicellar technology is a technology based on lipidic compositions, which form an optimal dispersed phase in the gastrointestinal environment for improved absorption of insoluble drugs.
