SALT LAKE CITY, March 28, 2017 (GLOBE NEWSWIRE) -- Lipocine Inc. (NASDAQ:LPCN), a specialty pharmaceutical company, today announced that Mahesh
Patel, President and CEO, and Morgan Brown, Executive Vice President and CFO, will present a company overview at the
16th Annual Needham Healthcare Conference on Tuesday, April 4, 2017 at 9:20 a.m. ET.
A live audio webcast of the presentation will be available via the "Investor Relations" page of the Lipocine
website, www.lipocine.com. Please log on through Lipocine's website approximately 10 minutes prior
to the scheduled start time. A replay of the webcast will also be archived on Lipocine's website for 90 days following the
presentation
About Lipocine
Lipocine Inc. is a specialty pharmaceutical company developing innovative pharmaceutical products for use in men's
and women's health using its proprietary drug delivery technologies. Lipocine’s clinical development pipeline includes three
development programs LPCN 1021, LPCN 1111 and LPCN 1107. LPCN 1021, a novel oral prodrug of testosterone containing
testosterone undecanoate, is designed to help restore normal testosterone levels in hypogonadal men. LPCN 1021, was well tolerated
and met the primary efficacy end-point in Phase 3 testing, which utilized 24-hour pharmacokinetic data for dose adjustments, and is
currently being studied in two additional Phase 3 clinical trials. LPCN 1111, a novel oral prodrug of testosterone,
originated with and is being developed by Lipocine as a next-generation oral testosterone product with potential for once-daily
dosing and is currently in Phase 2 testing. LPCN 1107, the potentially first oral hydroxyprogesterone caproate product
candidate indicated for the prevention of recurrent preterm birth, has been granted orphan drug designation by the FDA. An End of
Phase 2 meeting with the FDA has been completed. For more information, please visit www.lipocine.com.
Forward-Looking Statements
This release contains “forward looking statements” that are made pursuant to the safe harbor provisions of the
Private Securities Litigation Reform Act of 1995 and include statements that are not historical facts regarding Lipocine’s product
candidates and related clinical trials and the FDA review process relating to its product candidates, plans related to clinical
trials, the possible outcome and timing of such clinical trials, the expected timing of clinical trial results or any related FDA
review process, the path to approvability by the FDA of Lipocine’s development programs, the potential uses and benefits of our
product candidates, and our product development efforts. Investors are cautioned that all such forward-looking statements involve
risks and uncertainties, including, without limitation, the risks that the FDA will not approve any of our products, risks related
to our products, expected product benefits not being realized, clinical and regulatory expectations and plans not being realized,
advance regulatory developments and requirements, risks related to the FDA approval process, the receipt of regulatory approvals,
the results and timing of clinical trials, patient acceptance of Lipocine’s products, the manufacturing and commercialization of
Lipocine’s products, and other risks detailed in Lipocine’s filings with the SEC, including, without limitation, its Form 10-K and
other reports on Forms 8-K and 10-Q, all of which can be obtained on the SEC website at www.sec.gov. Lipocine assumes no obligation to update or revise publicly any forward-looking
statements contained in this release, except as required by law.
CONTACT: Morgan Brown Executive Vice President & Chief Financial Officer Phone: (801) 994-7383 mb@lipocine.com Investors: Hans Vitzhum Phone: (646) 597-6979 hans@lifesciadviors.com
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