0001085037-11-000229.txt : 20110712 0001085037-11-000229.hdr.sgml : 20110712 20110712172930 ACCESSION NUMBER: 0001085037-11-000229 CONFORMED SUBMISSION TYPE: 6-K PUBLIC DOCUMENT COUNT: 1 CONFORMED PERIOD OF REPORT: 20110712 FILED AS OF DATE: 20110712 DATE AS OF CHANGE: 20110712 FILER: COMPANY DATA: COMPANY CONFORMED NAME: REPLICEL LIFE SCIENCES INC. CENTRAL INDEX KEY: 0001205059 STANDARD INDUSTRIAL CLASSIFICATION: GOLD & SILVER ORES [1040] IRS NUMBER: 000000000 STATE OF INCORPORATION: A1 FISCAL YEAR END: 1231 FILING VALUES: FORM TYPE: 6-K SEC ACT: 1934 Act SEC FILE NUMBER: 000-50112 FILM NUMBER: 11964543 BUSINESS ADDRESS: STREET 1: SUITE 1225 - 888 DUNSMUIR STREET CITY: VANCOUVER BC STATE: A1 ZIP: V6C 3K4 BUSINESS PHONE: 604-248-8730 MAIL ADDRESS: STREET 1: SUITE 1225 - 888 DUNSMUIR STREET CITY: VANCOUVER BC STATE: A1 ZIP: V6C 3K4 FORMER COMPANY: FORMER CONFORMED NAME: NEWCASTLE RESOURCES LTD. DATE OF NAME CHANGE: 20081128 FORMER COMPANY: FORMER CONFORMED NAME: PAN AMERICAN GOLD CORP DATE OF NAME CHANGE: 20040521 FORMER COMPANY: FORMER CONFORMED NAME: TRI LATERAL VENTURE CORP DATE OF NAME CHANGE: 20021109 6-K 1 f6k071211.htm FORM 6-K f6k071211.htm

 
UNITED STATES
 
SECURITIES AND EXCHANGE COMMISSION
 
Washington, D.C.  20549
 
 
Form 6-K
 
 
REPORT OF FOREIGN PRIVATE ISSUER PURSUANT TO RULE 13a-16 OR 15d-16 UNDER THE SECURITIES EXCHANGE ACT OF 1934
 
 
For the month of  June 2011
 
 
Commission File Number  000-50112
 
 
RepliCel Life Sciences Inc.
(Translation of registrant’s name into English)
 
 
Suite 1225 – 888 Dunsmuir Street, Vancouver, British Columbia  V6C 3K4
(Address of principal executive office)
 
 
Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.     Form 20-F  [X]  Form 40-F  [  ]
 
 
Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1)  [  ]
 
 
Note:  Regulation S-T Rule 101(b)(1) only permits the submission in paper of a Form 6-K if submitted solely to provide an attached annual report to security holders.

 
 

 
BRITISH COLUMBIA
ONTARIO
 
FORM 51-102F3
 
MATERIAL CHANGE REPORT
 
Item 1.  
Name and Address of Company
 
Replicel Life Sciences Inc. (the “Company”)
(formerly Newcastle Resources Ltd.)
Suite 1225 – 888 Dunsmuir Street
Vancouver, BC V6C 3K4
 
Item 2.  
Date of Material Change
 
June 22, 2011 and July 1, 2011
 
Item 3.  
News Release
 
 News Release dated July 1, 2011 was disseminated via Marketwire on July 1, 2011.
 
Item 4.  
Summary of Material Change
 
The Company announced that it filed a continuation application with the Province of British Columbia and, effective June 22, 2011, redomiciled from the Province of Ontario to the Province of British Columbia under the new name of “RepliCel Life Sciences Inc.”.  The Financial Industry Regulatory Authority (FINRA) approved the name change and redomicile and, effective July 1, 2011, the Company’s stock began trading under the symbol “REPCF”.
 
Item 5.  
Full Description of Material Change
 
5.1         Full Description of Material Change
 
See attached news release.
 
5.2         Disclosure for Restructuring Transactions
 
N/A
 
Item 6.  
Reliance on subsection 7.1(2) or (3) of National Instrument 51-102
 
Not Applicable.
 
Item 7.  
Omitted Information
 
Not Applicable.
 
Item 8.  
Executive Officer
 
David Hall
President and Director
604.684.4312

 
2

 
 
Item 9.  
Date of Report

          July 12, 2011

 
3

 
RepliCel Redomiciles to British Columbia and Finalizes Name and Stock Symbol Change
 
VANCOUVER, BC – July 1, 2011 - RepliCel Life Sciences (OTCBB: REPCF) is pleased to announce that, on June 22, 2011, it filed a continuation application with the Province of British Columbia and, effective on such date, redomiciled from the Province of Ontario to the Province of British Columbia under the new name of “RepliCel Life Sciences Inc.”. The Financial Industry Regulatory Authority (FINRA) has approved the name change and redomicile and, effective July 1, 2011, the Company’s stock will begin trading under the symbol “REPCF”.
 
The name and symbol change is the final step in a series of corporate changes to the business focus of the Company in the area of autologous cell therapy. The first medical condition being pursued in clinical human trials is hair cell replication and hair regeneration through the development and delivery of a safe, natural, minimally invasive surgical procedure.
 
About RepliCel Life Sciences
 
The Company has developed RepliCel™, a natural hair cell replication technology that has the potential to become the world’s first, minimally invasive solution for androgenetic alopecia (pattern baldness) 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, the Company hopes to initiate natural hair regeneration. Patents for the technology have been issued by the European Union and Australia and are pending in other major international jurisdictions. The RepliCel™ procedure has been developed over the past nine years by the Company’s recognized research scientists and medical experts – specialists in the fields of hair growth, hair biology and dermatology. Additional information on RepliCel is available at www.replicel.com.
 
Contact:
 
Tammey George, Director of Communications
Telephone: 6042488730
tg@replicel.com
 
Notice Regarding Forward Looking Statements
 
This press release contains projections and forwardlooking statements, as that term is defined under applicable securities laws. Statements in this press release, which are not purely historical, are forwardlooking statements and can include, without limitation, statements based on current expectations involving a number of risks and uncertainties which are not guarantees of future performance of the Company such as the statement that the RepliCelTM hair cell replication technology has the potential to become the world’s first minimally invasive solution for androgenetic alopecia (pattern baldness) 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 forwardlooking information, including: negative results from the Company’s clinical trials, including that the Company’s hair cell replication technology may not work as planned or may not be effective at causing the regrowth of hair follicles or the rejuvenation of damaged, miniaturized follicles; the effects of government regulation on the Company’s business; the viability and marketability of the Company’s hair cell replication technology; the Company’s failure to successfully implement its marketing plan; the development of superior technology by the Company’s competitors; the failure of consumers and the medical community to accept the Company’s technology as safe and effective; risks associated with the Company’s ability to obtain and protect rights to our intellectual property; risks and uncertainties associated with the Company’s ability to raise additional capital; and other factors beyond the Company’s control. Although the Company believes that the expectations reflected in the forwardlooking

 
4

 
statements are reasonable, it cannot guarantee future results, levels of activity or performance. Further, any forwardlooking statement speaks only as of the date on which such statement is made, and, except as required by applicable law, the Company undertakes no obligation to update any forwardlooking statement to reflect events or circumstances after the date on which such statement is made or to reflect the occurrence of unanticipated events. New factors emerge from time to time, and it is not possible for management to predict all of such factors and to assess in advance the impact of such factors on the Company’s business or the extent to which any factor, or combination of factors, may cause actual results to differ materially from those contained in any forwardlooking statement. 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 20F for the fiscal year ended December 31, 2010 and other periodic reports filed from timetotime with the Securities and Exchange Commission on EDGAR at www.sec.gov and with the Canadian Securities Commissions on SEDAR at www.sedar.com.

 
5

 
SIGNATURES
 
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
RepliCel Life Sciences Inc.
 
/s/ David Hall                                                      
David Hall, President
Date:  July 12, 2011

 
6