RepliCel Life Sciences Inc.

RepliCel Life Sciences Inc.

September 10, 2012 09:30 ET

RepliCel to Present at Rodman and Renshaw Global Investment Conference

VANCOUVER, BRITISH COLUMBIA--(Marketwire - Sept. 10, 2012) - RepliCel Life Sciences Inc.'s (the "Company" or "RepliCel") (OTCBB:REPCF) today announces that David Hall, CEO and President, will be presenting at the Rodman & Renshaw Global Investment Conference. Mr. Hall is scheduled to present on September 11th at 2:25 PM ET in the Starlight South suite at the Waldorf Astoria hotel in New York. The 20 minute presentation will include an update on corporate events and plans for a Phase II dose-ranging trial using RepliCel™ as a potential treatment for hair loss in men and women. The presentation will be webcast and posted on Rodman and Renshaw's website at and on RepliCel's website at in the media section.

About RepliCel Life Sciences Inc.

The Company has developed RepliCel™, a patented natural hair cell replication technology that has the potential to become the world's first, minimally invasive solution for androgenetic alopecia and general hair loss in men and women. RepliCel™ is based on autologous cell implantation technology that replicates a patient's hair cells from their own healthy hair follicles and, when reintroduced into areas of hair loss, initiates natural hair regeneration. The Company is currently conducting first-in-man clinical trials. Additional information on RepliCel is available at

Notice Regarding Forward-Looking Statements

This press release contains forward-looking statements, including but not limited to: states that the Company will complete a Phase II clinical trial and that RepliCel™ has the potential to become the world's first, minimally invasive solution for androgenetic alopecia and general hair loss in men and women. These statements are only predictions and involve known and unknown risks which may cause actual results and the Company's plans and objectives to differ materially from those expressed in the forward-looking statements. These risks and uncertainties include: whether the Company can obtain regulatory approval for its planned Phase II clinical trial; that negative results may result from the Company's clinical trials; the effects of government regulation on the Company's business; risks associated with the Company's ability to obtain and protect rights to its intellectual property; risks and uncertainties associated with the Company's ability to raise additional capital to carry out its planned activities; and other factors beyond the Company's control. Although the Company believes that the expectations reflected in the forward-looking statements are reasonable, it cannot guarantee future results, levels of activity or performance. Readers should consult all of the information set forth herein and should also refer to the risk factor disclosure outlined in the Company's annual report on Form 20-F for the fiscal year ended December 31, 2011, and other periodic reports filed from time-to-time with the Securities and Exchange Commission on Edgar at and with the British Columbia Securities Commission on SEDAR at

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