Mr. Andrew Schutte reports

REPLICEL ANNOUNCES THE PASSING OF LONG TIME CHIEF FINANCIAL OFFICER SIMON MA; DAVID KWOK IS APPOINTED CHIEF FINANCIAL OFFICER

RepliCel Life Sciences Inc. has changed chief financial officers.

With great sorrow, RepliCel announces the passing of Simon Ma, our long-tenured chief financial officer. "Simon Ma has been a valuable member of the team for many years, Simon's deep commitment to the company was always evident. We spent many late nights engaged on projects together. Simon's commitment was unwavering, and he left an enduring impact on our team and his legacy of integrity and leadership will continue to inspire us," president and chief executive officer Andrew Schutte stated.

David Kwok steps into the chief financial officer role with a clear financial vision for the company's success. His extensive expertise, honed while working with numerous public companies, positions RepliCel for the future. "David Kwok's experience and expertise position him well to assume the role of chief financial officer, David's experience with public companies for over 15 years will prove invaluable," Mr. Schutte stated. Mr. Kwok has been a certified professional accountant for over 15 years and is a member of the Certified Professional Accountant of British Columbia since January, 2008.

In connection with the appointment of Mr. Kwok, the company has granted 150,000 stock options to Mr. Kwok for the purchase of up to 150,000 common shares of the company pursuant to its 10 per cent rolling stock option plan. Each option is exercisable until Aug. 16, 2027, at a price of 15 cents per common share and vest upon the date of grant.

In light of Mr. Ma's sudden passing, RepliCel will apply for a management cease trade order (MCTO) as the company completes a transition process and endeavours to file its second quarter financials in a timely manner.

About RepliCel Life Sciences Inc.

RepliCel is a regenerative medicine company focused on developing cell therapies for aesthetic and orthopedic conditions affecting what the company believes is approximately one in three people in industrialized nations, including aging/sun-damaged skin, pattern baldness and chronic tendon degeneration. These conditions, often associated with aging, are caused by a deficit of healthy cells required for normal tissue healing and function. These cell therapy product candidates are based on RepliCel's innovative technology, utilizing cell populations isolated from a patient's healthy hair follicles.

The company's cell therapy product pipeline comprises RCT-01 for tendon repair, RCS-01 for skin rejuvenation and RCH-01 for hair restoration. RCH-01 has been the subject of successful safety and dose-finding clinical studies, and is now the subject of its third clinical study evaluating efficacy for the treatment of male and female hair loss due to androgenetic alopecia. This continuing study is being financed by Shiseido Company Ltd. pursuant to a licence agreement, which has now been terminated but is the subject of an arbitration regarding Shiseido's rights to the product for Asia. RepliCel maintains the undisputed rights to RCH-01 for the rest of the world. RCT-01 and RCS-01 are exclusively licensed in greater China to Yofoto (China) Health Company. RepliCel and Yofoto are currently co-developing these products in China. RepliCel maintains the rights to these products outside of greater China.

RepliCel has also developed a proprietary injection device (DermaPrecise) and related consumables, expected to improve the administration of its cell therapy products and certain other injectables. Yofoto has exclusively licensed the commercial rights for the DermaPrecise device and consumables in greater China for dermatology applications, and is expected to first launch the product in Hong Kong upon it being approved for market launch in either the United States or Europe. MainPointe Pharmaceuticals has an exclusive distribution agreement for the DermaPrecise device and consumables in the United States, subject to income. MainPointe is expected to finance the U.S. Food and Drug Administration (FDA) approval process in the United States.