Form 10QSB (09-30-06)

U. S. SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

FORM 10-QSB



[X]
QUARTERLY REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended September 30, 2006

[ ]
TRANSITION REPORT UNDER SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from ___________ to _____________


Commission File Number: 0-32917

PROTOKINETIX, INC.

Nevada
94-3355026
(State or other jurisdiction of
incorporation or organization)
(I.R.S. Employer
Identification No.)
 
Suite 1500-885 West Georgia Street
Vancouver, British Columbia Canada V6C3E
________________________________________________________________________
(Address of principal executive offices, including zip code)
 
Registrant’s telephone number, including area code:  (604) 687-9887
Securities registered pursuant to Section 12(b) of the Act:  None
Securities registered pursuant to Section 12(g) of the Act:  $.0000053 par value common stock

Check whether the issuer (1) filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act of 1934 during the past 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.  Yes X  No ___
 
Indicate by a check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act. Yes _ No X

APPLICABLE ONLY TO ISSUERS INVOLVED IN BANKRUPTCY
PROCEEDINGS DURING THE PRECEDING FIVE YEARS

Check whether the registrant filed all documents and reports required to be filed by Section 12, 13, or 15(d) of the Exchange Act of 1934 after the distribution of securities under a plan confirmed by a court. Yes ___ No ____

APPLICABLE ONLY TO CORPORATE ISSUERS

State the number of shares outstanding of each of the issuer’s classes of common equity, as of the latest practicable date:

44,060,153 common shares outstanding, $0.0000053 par value, at October 30, 2006.


Transitional Small Business Disclosure Format: Yes __ No X

 
 
 


PART I


ITEM 1. FINANCIAL STATEMENTS

In accordance with Item 310 of Regulation S-B, our Financial Statements and Explanatory Notes are attached on the “F” pages at the end of this Report.

ITEM 2. MANAGEMENT’S DISCUSSION AND ANALYSIS OR PLAN OF OPERATIONS

 
The below discussion is furnished in accordance with Item 303 of Regulation S-B.

FORWARD-LOOKING STATEMENTS

This discussion and analysis in this Quarterly Report on Form 10-QSB should be read in conjunction with the accompanying Consolidated Financial Statements and related notes. Our discussion and analysis of our financial condition and results of operations are based upon our consolidated financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States. The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires us to make estimates and assumptions that affect the reported amounts of assets and liabilities, disclosure of any contingent liabilities at the financial statement date and reported amounts of revenue and expenses during the reporting period. We review our estimates and assumptions on an on-going basis. Our estimates are based on our historical experience and other assumptions that we believe to be reasonable under the circumstances. Actual results are likely to differ from those estimates under different assumptions or conditions, but we do not believe such differences will materially affect our financial position or results of operations. Our critical accounting policies, the policies we believe are most important to the presentation of our financial statements and require the most difficult, subjective and complex judgments, are outlined below in ‘‘Critical Accounting Policies,’’ and have not changed significantly.
 
In addition, certain statements made in this report may constitute “forward-looking statements” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements involve known or unknown risks, uncertainties and other factors that may cause the actual results, performance, or achievements of the Company to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Specifically, but not limited to, 1) our ability to obtain necessary regulatory approvals for our products; and 2) our ability to increase revenues and operating income, is dependent upon our ability to develop and sell our products, general economic conditions, and other factors. You can identify forward-looking statements by terminology such as "may," "will," "should," "expects," "intends," "plans," "anticipates," "believes," "estimates," "predicts," "potential," "continues" or the negative of these terms or other comparable terminology. We base these forward-looking statements on our expectations and projections about future events, which we derive from the information currently available to us. Such forward-looking statements relate to future events or our future performance. Although we believe that the expectations reflected-in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance or achievements. Forward-looking statements are only predictions. The forward-looking events discussed in this Quarterly Report, the documents to which we refer you, and other statements made from time to time by us or our representatives, may not occur, and actual events and results may differ materially and are subject to risks, uncertainties, and assumptions about us. For these statements, we claim the protection of the “bespeaks caution” doctrine. The forward-looking statements speak only as of the date hereof, and we expressly disclaim any obligation to publicly release the results of any revisions to these forward-looking statements to reflect events or circumstances after the date of this filing.

Critical Accounting Policies

Our critical and significant accounting policies, including the assumptions and judgments underlying them, are disclosed in the Notes to the Financial Statements. These policies have been consistently applied in all material respects and address such matters as revenue recognition and depreciation methods. The preparation of the financial statements in conformity with generally accepted accounting principles in the United States requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reported period. Actual results could differ from those estimates. The accounting treatment of a particular transaction is specifically dictated by accounting principles, generally accepted in the United States of America, with no need for management’s judgment in their application. There are also areas in which management’s judgment in selecting any viable alternative would not produce a materially different result. See our audited financial statements and notes thereto which contain accounting policies and other disclosures required by accounting principles, generally accepted in the United States of America.

Overview

We are a biotechnical company headquartered in Vancouver, British Columbia that owns the world-wide rights to a family of synthetic anti-freeze glycoproteins (trademarked by us as AAGP™). We are dedicated to the commercial development of AAGP™ for use in human and veterinary medicine, food additives and supplements, and the biotechnology and cosmetic industry. We are making rapid and meaningful progress in this domain by coordinating a team of world recognized intellectual talent in a networked environment. This team has been able to use previously published research on native antifreeze proteins and antifreeze glycoproteins as a guide to the expansion and development of markets for this valuable family of molecules.

The ProtoKinetix business plan is based primarily on the furtherance of certain intellectual property rights obtained by way of "sub-licenses" of technology from other companies. At present, we have engaged the patent law firm of Cabinet-Moutard of Versaille, France, and have filed a number of international patent applications. These patent applications include:
 
WO 2004/014928 A2 (19 February 2004)
PCT Int. Appl. (2006), 87 pp. WO2006059227 A1 20060608 AN 2006:538719
Patent application: Fr 03 May 2006, 06 03952

Consistent with our agreements with the licensors of various technologies we license, we have no finished commercial product or products, and have received no final patents awards or FDA approvals for any product or diagnostic procedures. We are focused on the research and development of one primary compound known as AFGP, which we have filed a trademark application for.

Employees

We currently have no full time employees. We operate with a skeletal management team headed by Dr. John Todd, M.D. In addition to Dr. Todd, we receive advice and counsel from our Scientific Advisory Board.

Our Main Project

We are currently developing and testing synthetic antifreeze glycoproteins (AFGP). We have entered into agreements which give the exclusive right to develop products derived from patent pending technologies related to synthetic AFGPs. Our intellectual property rights were developed by Dr. Geraldine Castelot-Deliencourt.

Background on our AFGP Project

One of many accomplishments from pioneering research of the U.S. Antarctic Program was the discovery, in the early sixties, that fish living year-long in subzero temperature are extremely resistant to freezing. The substances that prevent these fish from freezing were isolated, characterized and designated as antifreeze glycoproteins or AFGP. Over the years, various kinds of AFGP were isolated from many species of fishes, and in some amphibians, plants and insects. All of the AFGPs share a common characteristic that prevents ice crystals from growing and connecting to each other. There has also been research done on the membrane stabilizing characteristics of native AFGP.

A review of the scientific literature will confirm that there has been a great deal of interest around the world in these natural antifreeze glycoproteins which are able to protect a great many creatures which are subjected to freezing temperatures. A further review will also confirm that the natural antifreeze is able to preserve mammalian cells tissue and organs. The metabolic rate in living cells is reduced as the temperature is lowered. Keeping cells and tissue at a low temperature enables their preservation for a longer time than cells can be preserved for at a higher temperature. Yet, when cells are exposed to sub zero temperatures, they are destroyed by the formation of ice crystals which disrupts the cell membrane.

Scientists have conducted many experiments in which they extracted naturally occurring AFGP from a variety of fish and then used these naturally occurring antifreeze glycoproteins to reduce the temperature at which ice crystals are formed. It has been determined in experiments by many scientists that mammalian cells in a solution containing natural AFGP could be successfully preserved at temperatures several degrees below zero Celsius. At this temperature the metabolic rate of the cells is very low, and these cells can be preserved for a longer period of time at sub zero temperatures as long as the cells are not destroyed by the formation of ice crystals. However, until today, applications of AFGP were limited since researchers were unable to produce sufficient quantities or stable enough copies of these antifreeze glycoproteins for commercial applications, and the use of naturally occurring compounds extracted from fish is too labor and cost-intensive to be practical.

Sugar based molecules have long been known to be biologically active. Yet, the oxygen-glycosidic link is readily cleaved by glycosidases, resulting in a low bio-availability of these glycoconjugate based molecules. Dr. Geraldine Castelot-Deliencourt, along with Dr. Jean-Charles Quirion at the Research Institute of Organic Chemistry in Rouen, France, has developed a patented process to stabilize the oxygen-glycosidic bond in these sugar based molecules. This patented process replaces the weaker oxygen bond with a C-F2 mimetic. The resultant molecules are biologically active, are stable over a pH range of 2 to 13, and are not broken down by glycosidases. It is by using this patented process that the active repeating segment of native antifreeze glycoproteins has been synthesized to produce the synthetic antifreeze glycoprotein molecules (AAGP™). Protokinetix Inc. has produced and tested a variety of the molecules from the family of AAGP™ molecules. The experimental work which we have conducted confirms the following:

·  
The molecules are stable over a pH of 1.8 to 13
·  
There is no toxicity demonstrated in 2 separate trials
·  
There is excellent preservative effect upon cells, protecting them from harsh environmental stimuli. This was confirmed using Ultraviolet C radiation and 1 molar solution of Hydrogen Peroxide
·  
There is no interference with cell growth rate
·  
Cells appear morphologically normal in the presence of AAGP™
·  
Cells function normally in the presence of AAGP™
·  
There is a reduced COX-2 induction following an inflammatory stimulus (Interleukin 1-B). The IL1-B/COX2 pathways is a well known pathway involved in many pathologies.
·  
There is strong evidence to show that AAGP™ is involved in cellular repair at the molecular level
·  
AAGP™ has been shown to enhance cell viability after cryopreservation
·  
Cells live significantly longer in the presence of AAGP™ over a temperature range of minus 3 degrees C to plus 37 degrees C
·  
AAGP enables the preservation of Platelets at minus 3 degrees C.

We are continuing our research to determine additional characteristics of AAGP™ as well as the mechanism of action of this very interesting and valuable family of molecules. The work is being conducted not only through our contracted researchers but also through a number of universities. The results of our work to date suggest that AAGP™ may have a very large market in the following areas:

1.  
Skin Care
a.  
Anti-aging
b.  
Reparative
c.  
Protective
d.  
Solar Block

2.  
Cell culture protection
a.  
Short term preservation
b.  
Cryopreservation

3.  
Organ Preservation for Transplantation
a.  
Cells - Islet cell transplantation
b.  
Solid organ

4.  
Tissue preservation
a.  
Cardioplegic solution additive
b.  
Tissue damage reduction following CVA and MI
c.  
Tissue protection following trauma and ischemia secondary to edema

5.  
Blood and blood product preservation
a.  
Platelet storage
b.  
Long term storage of packed red cells
 
Intellectual Property

As of the date of this Report, our development agents, including the parties we have licensed AFGP technologies from, have applied to receive patents for technologies we have licensed and continue to primarily base our research efforts on. At present, we have engaged the patent law firm of Cabinet-Moutard of Versaille, France, and have filed a number of international patent applications. These patent applications include:
 
WO 2004/014928 A2 (19 February 2004)
PCT Int. Appl. (2006), 87 pp. WO2006059227 A1 20060608 AN 2006:538719
Patent application: Fr 03 May 2006, 06 03952

Consistent with our agreements with the licensors of various technologies we license, we have no finished commercial product or products, and have received no final patents awards or FDA approvals for any product or diagnostic procedures. We are focused on the research and development of one primary compound known as AFGP, which we have filed a trademark application for.

Subject to our available financial resources, our intellectual property strategy is: (1) to pursue licenses, trade secrets, and know-how within our primary research areas, and (2) to develop and acquire proprietary positions to reagents and new platforms for the development of products related to these technologies.

Trade Secrets and Know-How

We believe that even if our intellectual property position is ultimately diminished as a result of our development agents and licensors to receive patent protection for the licenses ProtoKinetix has contracted to access, we have developed a substantial body of trade secrets and know-how relating to the development of AAGP™, including but not limited to the optimization of materials for efforts, and how to maximize sensitivity, speed-to-result, specificity, stability and reproducibility.

Competition

The markets that we are attempting to enter are multi-billion dollar international industries. They are intensely competitive. Many of our competitors (from every perspective) are substantially larger and have greater financial, research, manufacturing, and marketing resources.

Industry competition in general is based on the following:

·  
Scientific and technological capability;
·  
Proprietary know-how;
·  
The ability to develop and market products and processes;
·  
The ability to obtain FDA or other required regulatory approvals;
·  
The ability to manufacture products that meet applicable FDA requirements, (i.e. FDA’s Quality System Regulations) see Governmental Regulation section;
·  
Access to adequate capital;
·  
The ability to attract and retain qualified personnel; and
·  
The availability of patent protection.

We believe our scientific and technological capabilities are significant. Some of the results of our research are available at our website located at www.protokinetix.com.

Our ability to develop our research is in large measure dependent on our having additional resources and/or collaborative relationships, particularly where we can have our product development efforts funded on a project or milestone basis. We believe that our know-how with our AFGP project, in spite of not yet receiving any patent protected rights, has been instrumental in our obtaining the collaborations we have developed.
 
Although there is no such immediate need to make any regulatory filing in the United States or abroad, you should be aware that we have limited experience with regard to obtaining FDA or other required regulatory approvals, and no experience with obtaining pre-marketing approval of a biologic product. For this reason, should our research efforts continue to show promise, we will likely need to hire consultants to assist us with such governmental regulations.

Our access to capital is more challenging, relative to most of our competitors. This is a competitive disadvantage. We believe, however, that our access to capital may increase as we get closer to the development of a commercially viable product.

To date, we believe our research has enabled us to attract and retain qualified consultants. Because of the greater financial resources of many of our competitors, we may not be able to complete effectively for the same individuals to the extent that a competitor uses its substantial resources to attract any such individuals.

As is discussed above, with respect to the availability of patent protection, we do not have our own portfolio of patents or the financial resources to develop and/or acquire a portfolio of patents similar to those of our larger competitors. We have been able to obtain access to patent-pending technology by entering into licensing arrangements. However, there can be no certainty that any of the patent-pending technologies we have licensed will ever receive final approval by any patent office.

Plan of Operation

Our current operations are centered around our relationships with various research and development consultants who are conducting research on our behalf at discrete and established laboratories in various parts of the world. We intend to continue these efforts for the next 12 months and believe, that due to our relatively minimal cash obligations, that we can satisfy our cash requirements during this period. We intend to help meet our corporate obligations by selling our common stock. However our common stock is at a low price and is not actively traded.

Sales and Marketing

We are not currently selling or marketing any products.

Expenses

Expenses for the three month period ending September 30, 2006 arose primarily from professional and consulting fees. We incurred professional fees relating to costs associated with our being a reporting company under the Securities Exchange Act of 1934, as amended. We also incurred consulting fees which contributed to a net loss of $300,845 during the three month period ended September 30, 2006.

Liquidity and Capital Resources

At September 30, 2006, we had $268,491 in cash and $277,840 in total current assets. As of the date of this report, we do not believe that we require additional capital investments or borrowed funds to meet cash flow projections and carry forward our business objectives. In the event that we need to raise additional capital, there can be no assurance that we will be able to raise capital from outside sources in sufficient amounts to fund our new business.

The failure to secure adequate outside funding would have an adverse affect on our plan of operation and results therefrom and a corresponding negative impact on shareholder liquidity.

Inflation

Although management expects that our operations will be influenced by general economic conditions, we do not believe that inflation had a material effect on our results of operations for the period ending September 30, 2006.

Going Concern

The accompanying financial statements have been prepared in conformity with generally accepted accounting principles, which contemplate our continuation as a going concern. The history of losses and our inability to make a profit from selling a good or service has raised substantial doubt about our ability to continue as a going concern.

Results of Operations for the Period Ending September 30, 2006

We had $0 in net revenues for the period ending September 30, 2006.

We sustained a $300,845 loss from continuing operations for the three month period ending September 30, 2006.

Operating expenses were $300,845 for the three month period ending September 30, 2006. These expenses were primarily incurred for professional fees, consulting services related to the operations of the Company's business, specifically, research and development related expenses, and other general and administrative expenses.


ITEM 3. CONTROLS AND PROCEDURES

As required by Rule 13a-15 under the Securities Exchange Act of 1934 (“Exchange Act”) we carried out an evaluation of the effectiveness of the design and operation of our disclosure controls and procedures as of September 30, 2006, being the date of our most recently completed fiscal quarter. This evaluation was carried out under the supervision and with the participation of our Chief Executive Officer and Chief Financial Officer. Based upon that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and procedures are effective to ensure that information required to be disclosed in our Exchange Act reports is recorded, processed, summarized, and reported within the time periods specified in the Securities and Exchange Commission’s rules and forms, and that such information is accumulated and communicated to them to allow timely decisions regarding required disclosure.

During our most recently completed quarter ended September 30, 2006, there were no changes in our internal control over financial reporting that have materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

PART II

ITEM 1. LEGAL PROCEEDINGS

We are not party to any legal proceedings and to our knowledge, no such proceedings are threatened or contemplated against us.


ITEM 2. UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS

On July 27, 2006, we issued 1,200,000 shares of our common stock registered on Form S-8 to various employees and consultants of the Company in connection with various employment and consultant agreements.

On August 11, 2006, we issued 100,000 restricted shares of our common stock to outside consultants in connection with a consulting agreement.

On September 8, 2006, we issued 69,231 shares of our common stock to outside consultant in connection with consulting agreements.

On September 12, 2006, we issued 186,406 shares of our common stock registered on Form S-8 and 114,347 restricted shares of our common stock to various outside consultants in connection with various consulting agreements.

Pursuant to Item 3.02 of Form 8-K, because the Company is a small business issuer and all of the above issuances, in the aggregate, equal less than 5% of the number of common shares issued and outstanding (based on the number of issued and outstanding shares identified in the Company's last periodic report), these sales were not reported in a Form 8-K.


ITEM 3. DEFAULT UPON SENIOR SECURITIES

None


ITEM 4. SUBMISSION OF MATTERS TO A VOTE OF SECURITY HOLDERS

No matters were submitted to our security holders for a vote during our first quarter ended September 30, 2006.


ITEM 5. OTHER INFORMATION

None


ITEM 6. EXHIBITS AND REPORTS ON FORM 8-K.

Ex. #
  
Description
     
3(i).1
  
Certificate of Incorporation filed as an exhibit to the Company's registration statement on Form 10SB/A filed on July 24, 2001 and incorporated herein by reference.
     
3(ii).1
  
By-Laws filed as an exhibit to the Company's registration statement on Form 10SB/A filed on July 24, 2001 and incorporated herein by reference.
     
14.1
  
ProtoKinetix, Inc. Code of Ethics filed as an exhibit to our annual report on Form 10-KSB filed on April 13, 2006.
     
31.1
  
Rule 13a-12(a)/15d-14(a) Certification of Chief Executive Officer and Chief Financial Officer pursuant to 18 U.S.C Section 1350, as adopted pursuant to Section 302 the Sarbanes-Oxley Act of 2002.
     
32.1
  
Certification of Chief Executive Officer and Chief Financial Officer pursuant to 18 U.S.C Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
     







 
 
 






Signatures

In accordance with Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

Protokinetix, Inc.
 
/s/ Dr. John Todd
____________________________
By: Dr. John Todd
Its: President, CEO and CFO
 

 
In accordance with the requirements of the Exchange Act, this report has been signed below by the following persons on behalf of the registrant and in the capacities and on the dates indicated.

Signatures
Title
Date
 
/s/Dr. John Todd
Dr. John Todd
 
Chief Executive Officer, President, Chief Financial Officer and Chairman Of The Board
 
November 15, 2006


 

 

 
 
 






PROTOKINETIX, INC.

FINANCIAL STATEMENTS

SEPTEMBER 30, 2006

(UNAUDITED)






 
 
 



PROTOKINETIX, INC.
BALANCE SHEET
September 30, 2006
(Unaudited)
         
     
ASSETS
  
         
Current Assets
  
 
Cash
  
$ 268,491
 
Accounts receivable
9,149
 
Prepaid expenses
200
         
   
Total current assets
277,840
         
Computer Equipment, net
1,698
Intangible Assets
3,110,000
       
$ 3,389,538
         
     
LIABILITIES AND STOCKHOLDERS' EQUITY
 
         
Current Liabilities
  
         
 
Due to outside management consultants
$ 306,892
 
Accounts payable
21,636
     
Total current liabilities
328,528
         
Long-term Debt
-
     
Total liabilities
328,528
         
Stockholders' Equity
 
         
 
Common stock, $.0000053 par value; 100,000,000 common
 
   
shares authorized; 44,160,153 shares issued and outstanding
 
236
 
Common stock issuable;400,000 shares
5
 
Additional paid-in capital
16,945,103
 
Deficit accumulated during the development stage
(13,884,334)
       
3,061,010
       
$ 3,389,538
         


See Notes To Financial Statements

 
 
 



PROTOKINETIX, INC.
STATEMENTS OF OPERATIONS
For the Three Months and Nine Months Ended September 30, 2006 and 2005, and for the
Period from December 23, 1999 (Date of Inception) to September 30, 2006
(Unaudited)
 
   
Three Months
Ended
September 30, 2006
  
Three Months
Ended
September 30, 2005
  
Nine Months
Ended
September 30, 2006
 
Nine Months
Ended
September 30, 2005
 
Cumulative During the Development Stage
Revenue
$ -
 
$ -
 
$ -
 
$ -
 
       $ 2,000
                   
Expenses
                  
                     
 
Professional fees
97,031
 
82,000
 
301,560
  
253,186
 
2,728,253
 
Consulting fees
80,000
 
(257,500)
  
1,525,256
 
3,135,476
 
9,562,935
 
Research and development
86,709
 
206,430
 
151,022
 
373,698
 
771,204
 
General and administrative
37,105
 
33,132
 
115,497
  
120,057
 
462,558
 
Impairment loss
-
 
-
 
-
 
-
 
269,756
 
Interest
-
 
2,466
 
11,869
 
10,727
 
48,162
   
300,845
 
66,528
 
2,105,204
 
3,893,144
 
13,842,868
 
Loss from continuing
                  
 
operations
(300,845)
  
(66,528)
  
(2,105,204)
  
(3,893,144)
  
(13,840,868)
Discontinued Operations
                  
 
Loss from operations of
                 
 
the discontinued statement
 
  
-
 
 
 
-
 
(43,466)
Net Loss
$ (300,845)
  
$ (66,528)
  
$(2,105,204)
 
$(3,893,144)
 
$(13,884,334)
                   
Net Loss per Share (basic and fully diluted)
$ (0.01)
  
$ (0.00)
  
$ (0.05)
 
$ (0.10)
 
  
                     
Weighted average shares
                 
 
outstanding
42,372,996
  
39,903,852
  
42,856,661
  
38,053,516
    
                     

See Notes To Financial Statements
 
 
 

 
 
 




PROTOKINETIX, INCORPORATED
   
                   
STATEMENTS OF STOCKHOLDERS' EQUITY
For the Period from December 23, 1999 (Date of Inception) to September 30, 2006
(Unaudited)
             
Deficit
Deficit
  
             
Accumulated
Accumulated
  
       
Common Stock
Additional
Stock
During the
 
   
Common Stock
Issuable
Paid-in
Subscription
Development
  
   
Shares
Amount
Shares
Amount
Capital
Receivable
Stage
Total
Issuance of common stock, December 1999
9,375,000
$ 50
-
$ -
$ 4,950
$ -
$ -
$ 5,000
Net loss for period
 
 
 
 
 
 
(35)
(35)
Balance, December 31, 2000
9,375,000
50
-
-
4,950
 
(35)
4,965
Issuance of common stock, April 2001
5,718,750
30
   
15,220
   
15,250
Net loss for year
  
 
 
 
 
 
 
(16,902)
(16,902)
Balance, December 31, 2001
15,093,750
80
-
-
20,170
 
(16,937)
3,313
Net loss for year
  
 
 
 
 
 
 
(14,878)
(14,878)
Balance, December 31, 2002
15,093,750
80
-
-
20,170
 
(31,815)
(11,565)
Issuance of common stock for services:
                
 
July 2003
2,125,000
11
   
424,989
   
425,000
 
August 2003
300,000
2
   
14,998
   
15,000
 
September 2003
1,000,000
5
   
49,995
   
50,000
 
October 2003
1,550,000
8
   
619,992
   
620,000
Issuance of common stock for licensing rights
14,000,000
74
   
2,099,926
   
2,100,000
Common stock issuable for licensing rights
    
2,000,000
11
299,989
   
300,000
Shares cancelled on September 30, 2003
(9,325,000)
(49)
    
49
   
-
Net loss for year
  
 
 
 
 
 
 
(1,262,745)
(1,262,745)
Balance, December 31, 2003
24,743,750
131
2,000,000
11
3,530,108
-
(1,294,560)
2,235,690
Issuance of common stock for services:
                
 
March 2004
1,652,300
9
   
991,371
   
991,380
 
May 2004
500,000
3
   
514,997
   
515,000
 
July 2004
159,756
1
   
119,694
   
119,695
 
August 2004
100,000
1
   
70,999
   
71,000
 
October 2004
732,400
4
   
479,996
   
480,000
 
November 2004
650,000
4
   
454,996
   
455,000
 
December 2004
255,000
1
   
164,425
   
164,426
Common stock issuable for AFGP license
    
1,000,000
5
709,995
   
710,000
Common stock issuable for Recaf License
    
400,000
2
223,998
   
224,000
Warrants granted (for 3,450,000 shares)
               
 
for services
                
 
October 2004
        
1,716,253
   
1,716,253
Options granted for services, October 2004
        
212,734
   
212,734
Stock subscriptions receivable
    
1,800,000
10
329,990
(330,000)
  
-
Warrants exercised:
              
-
 
August 2004
    
50,000
 
15,000
   
15,000
 
October 2004
    
600,000
3
134,997
   
135,000
 
December 2004
    
1,000,000
5
224,995
   
225,000
Options exercised, December 2004
    
100,000
1
29,999
   
30,000
Net loss for period
 
          
(5,388,274)
(5,388,274)
Balance, December 31, 2004
28,793,206
$ 154
6,950,000
$ 37
$ 9,924,547
$ (330,000)
$ (6,682,834)
$ 2,911,904
                   
                   
Issuance of stock subscriptions receivable
          
$ 240,000
 
240,000
Issuance of common stock for licensing rights
2,000,000
11
(2,000,000)
(11)
      
-
Issuance of stock for warrants exercised
2,050,000
10
(2,050,000)
(10)
      
-
Options exercised,
               
 
February 2005
    
35,000
1
10,499
   
10,500
 
May 2005
200,000
1
   
59,999
   
60,000
Note payable conversion, February 2005
    
285,832
1
85,749
   
85,750
Issuance of common stock for
               
Note payable conversion
               
 
April 2005
285,832
1
(285,832)
(1)
      
-
 
May 2005
353,090
2
   
105,925
   
105,927
Issuance of common stock for AFGP license
1,000,000
5
(1,000,000)
(5)
      
-
Issuance of common stock for
                
stock subscriptions received
1,400,000
6
(1,400,000)
(6)
  
90,000
 
90,000
Issuance of stock for options exercised
135,000
2
(135,000)
(2)
      
-
Issuance of common stock for services:
                
 
April 2005
30,000
1
   
14,999
   
15,000
 
May 2005
3,075,000
15
   
3,320,985
   
3,321,000
 
June 2005
50,000
1
   
50,499
   
50,500
 
August 2005
(250,000)
(1)
    
(257,499)
    
(257,500)
 
August 2005
111,111
1
(92,593)
(1)
15,000
   
15,000
 
October 2005
36,233
1
(36,233)
(1)
-
   
-
 
November 2005
                
 
November 2005
311,725
2
(245,000)
(1)
36,249
   
36,250
 
December 2005
1,220,000
8
   
756,392
   
756,400
                   
                   
Common stock issuable for services rendered
                
 
June 2005
    
200,000
1
149,999
   
150,000
 
August 2005
    
36,233
1
21,739
   
21,740
 
September 2005
    
125,000
1
74,999
   
75,000
 
September 2005(Proteocell)
    
100,000
1
57,999
   
58,000
 
December 2005
    
120,968
1
74,999
   
75,000
Net loss for the year
 
 
 
 
 
 
(5,096,296)
(5,096,296)
Balance, December 31, 2005
40,801,197
$ 220
608,375
$ 6
$14,503,079
$ -
(11,779,130)
$2,724,175
                   
                   
Common stock issuable:
                
 
February 2006
   
900,000
2
352,145
   
352,147
 
February/March 2006
   
20,000
1
10,499
   
10,500
Warrants granted from
               
private placement (450,000)
       
97,853
   
97,853
                   
Issuance of common stock for services:
                
 
March 2006
166,359
1
(108,375)
(1)
36,750
   
36,750
 
April 2006
(1,200,000)
(6)
    
6
   
-
 
May 2006
1,266,278
7
(70,000)
(1)
792,750
   
792,756
 
June 2006
27,056
 
1,200,000
6
718,244
   
718,250
 
July 2006
1,200,000
6
(1,200,000)
(6)
      
-
 
August 2006
100,000
1
   
64,999
   
65,000
 
September 2006
369,984
2
(50,000)
  
209,998
   
210,000
                   
Issuance of Private Placement
               
Stock (June 2006)
900,000
2
(900,000)
(2)
      
-
                   
Issuance of common stock for
               
Note payable conversion
                
 
May 2006
529,279
3
   
158,780
   
158,783
                   
Net loss for the period
 
 
 
 
 
 
(2,105,204)
(2,105,204)
                   
Balance, September 30, 2006
44,160,153
$ 236
400,000
$ 5
$16,945,103
$ -
$(13,884,334)
$3,061,010
                   

See Notes To Financial Statements

 
 
 




PROTOKINETIX, INC.
                 
STATEMENTS OF CASH FLOWS
For the Nine Months Ended September 30, 2006 and 2005, and for the
Period from December 23, 1999 (Date of Inception) to September 30, 2006
(Unaudited)
                 
                 
       
Nine Months Ended
September 30, 2006
  
Nine Months Ended
September 30, 2005
  
Cumulative During the Development Stage
Cash Flows from Operating Activities
          
 
Net loss for period
$ (2,105,204)
  
$ (3,893,144)
  
$ (13,884,334)
 
Adjustments to reconcile net loss to net cash
          
   
provided by (used in) operating activities
          
   
   Depreciation expense
763
  
674
  
1,690
   
   Write-off of Recaf license
        
269,756
 
Issuance of common stock for services
          
   
and expenses
1,833,256
  
3,433,740
  
10,056,147
 
Warrants issued for consulting services
-
  
-
  
1,716,253
 
Stock options issued for consulting services
-
  
-
  
212,734
 
Changes in operating assets and liabilities
          
   
Accounts receivable
(2,610)
      
(9,149)
   
Prepaid expenses
6,000
      
(200)
   
Due to outside management consultants
-
  
-
  
306,892
   
Accounts payable
(10,285)
  
14,569
  
20,802
   
Accrued interest payable
-
  
10,727
  
36,294
     
Net cash flows used in
          
     
  operating activities
(278,080)
  
(433,434)
  
(1,273,115)
Cash Flows from Investing Activities
          
 
Acquisition of intangible assets
-
  
-
  
(45,756)
 
Purchase of computer equipment
-
  
(1,959)
  
(3,388)
     
Net cash flows used in investing
          
     
   activities
-
  
(1,959)
  
(49,144)
Cash Flows from Financing Activities
          
 
Warrants exercised
-
  
240,000
  
705,000
 
Stock options exercised
-
  
70,500
  
100,500
 
Issuance of common stock for cash
450,000
  
-
  
470,250
 
Loan proceeds
    
-
  
315,000
     
Net cash flows provided by (used in)
          
     
financing activities
450,000
  
310,500
  
1,590,750
     
Net change in cash
171,920
  
(124,893)
  
268,491
Cash, beginning of period
96,571
  
283,556
    
Cash, end of period
$ 268,491
  
$ 158,663
  
$ (268,491)
Cash paid for interest
$ 12,703
  
$ -
  
$ 12,703
Cash paid for income taxes
$ -
  
$ -
  
$ -
                 
Supplementary information - Non-cash Transactions:
          
 
Common stock issuable for acquisition of intangible assets
$ -
  
$ -
  
$ 934,000
 
Stock subscriptions received
    
-
  
330,000
 
Note payable converted to common stock
158,783
  
191,677
  
350,460
                 


See Notes To Financial Statements

 
 
 


 
NOTES TO FINANCIAL STATEMENTS


Note 1. Organization and Significant Accounting Policies

Organization

ProtoKinetix, Incorporated (the "Company"), a development stage company, was incorporated under the laws of the State of Nevada on December 23, 1999. The Company is a medical research company whose mission is the advancement of human health care.

In 2003, the Company entered into an assignment of license agreement (the "Agreement") with BioKinetix, Inc., an Alberta, Canada, corporation. The Agreement provided the Company with an exclusive assignment of all of the rights (the "Rights") that BioKinetix possessed relating to two proprietary technologies that are being developed for the creation and commercialization of "superantibodies," an enhancement of antibody technology that makes ordinary antibodies much more lethal. In consideration, the Company's Board of Directors authorized the Company to issue 16,000,000 shares of its common stock to the shareholders of BioKinetix.

The Company is also currently researching the benefits and feasibility of proprietary synthesized Antifreeze Glycoproteins ("AFGP"). In preliminary studies, AFGP has demonstrated an ability to protect and preserve human cells at temperatures below freezing.

Interim Period Financial Statements

The interim period financial statements have been prepared by the Company pursuant to the rules and regulations of the U.S. Securities and Exchange Commission (the "SEC"). Certain information and footnote disclosure normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States have been condensed or omitted pursuant to such SEC rules and regulations. The interim period financial statements should be read together with the audited financial statements and accompanying notes included in the Company's audited financial statements for the years ended December 31, 2005 and 2004. In the opinion of the Company, the unaudited financial statements contained herein contain all adjustments (consisting of a normal recurring nature) necessary to present a fair statement of the results of the interim periods presented.

Going Concern

As shown in the financial statements, the Company has not developed a commercially viable product, has not generated any revenues to date and has incurred losses since inception, resulting in a net accumulated deficit at September 30, 2006. These factors raise substantial doubt about the Company's ability to continue as a going concern.

The Company needs additional working capital to continue its medical research or to be successful in any future business activities and continue to pay its liabilities. Therefore, continuation of the Company as a going concern is dependent upon obtaining the additional working capital necessary to accomplish its objective. Management is presently engaged in seeking additional working capital.

The accompanying financial statements do not include any adjustments to the recorded assets or liabilities that might be necessary should the Company fail in any of the above objectives and is unable to operate for the coming year.

Intangible Assets

The intangible assets consist of license rights to proprietary medical research technologies. The cost of the license rights is stated at cost or the value of the shares issued by the Company to acquire the license rights. The cost is not amortized because the licenses have indefinite lives. At September 30, 2006, management has determined that there is no impairment in the license rights that should be recorded against the carrying amount of the assets.

Earnings per Share

Basic loss per share is computed by dividing the net loss available to common shareholders by the weighted average number of common shares outstanding in the period. The Company's stock split 1:75 on August 24, 2001. In April 2002, the Board of Directors approved a 2.5 for 1 split of the Company's stock. The accompanying financial statements are presented on a post-split basis. The loss per share for the periods ended September 30, 2006 and 2005, have been adjusted accordingly. Diluted earnings per share takes into consideration common shares of outstanding (computed under basic earnings per share) and potentially dilutive securities. The effect of debt convertible into common shares was not included in the computation of diluted earnings per share for all periods presented because it was anti-dilutive due to the Company's losses. Common stock issuable is considered outstanding as of the original approval date for purposes of earnings per share computations.

Stock Based Compensation

Prior to January 1, 2006, the Company accounted for stock-based awards under the intrinsic value method, which followed the recognition and measurement principles of APB Opinion No. 25, “Accounting for Stock Issued to Employees”, and related Interpretations. The intrinsic value method of accounting resulted in compensation expense for stock options to the extent that the exercise prices were set below the fair market price of the Company’s stock at the date of grant.

As of January 1, 2006, the Company adopted SFAS No. 123(R) using the modified prospective method, which requires measurement of compensation cost for all stock-based awards at fair value on the date of grant and recognition of compensation over the service period for awards expected to vest. The fair value of stock options is determined using the Black-Scholes valuation model, which is consistent with the Company’s valuation techniques previously utilized for options in footnote disclosures required under SFAS No. 123, “Accounting for Stock Based Compensation”, as amended by SFAS No. 148, “Accounting for Stock Based Compensation Transition and Disclosure”.

Since the Company did not issue stock options to employees during the six months ended September 30, 2006 or 2005, there is no effect on net loss or earnings per share had the Company applied the fair value recognition provisions of SFAS No. 123(R) to stock-based employee compensation. When the Company issues shares of common stock to employees and others, the shares of common stock are valued based on the market price at the date the shares of common stock are approved for issuance.

New Accounting Pronouncements

In July 2006, the Financial Accounting Standards Board (FASB) issued FASB Interpretation (FIN) No. 48, “Accounting for Uncertainty in Income Taxes-an interpretation of FASB Statement No. 109.”  This Interpretation provides guidance for recognizing and measuring uncertain tax positions, as defined in Statement of Financial Accounting Standards (SFAS) No. 109, “Accounting for Income Taxes.”  FIN No. 48 prescribes a threshold condition that a tax position must meet for any of the benefit of an uncertain tax position to be recognized in the financial statements.  Guidance is also provided regarding derecognition, classification and disclosure of uncertain tax positions.  FIN No. 48 is effective for fiscal years beginning after December 15, 2006.  The Company does not expect that this Interpretation will have a material impact on their financial position, results of operations or cash flows.

In September 2006, the FASB issued Statement of Financial Accounting Standards No. 157, Fair Value Measurements (“FAS 157”). FAS 157 defines fair value, establishes a framework for measuring fair value and expands disclosures about fair value measurements but does not require any new fair value measurements. FAS 157 is effective for financial statements issued for fiscal years beginning after November 15, 2007, and interim periods within those fiscal years. The Company has not yet determined the impact of applying FAS 157.

In September 2006, the FASB issued Statement of Financial Accounting Standards No. 158, Employers’ Accounting for Defined Benefit Pension and Other Postretirement Plans, (“FAS 158”). FAS 158 requires an employer to recognize the overfunded or underfunded status of a defined benefit postretirement plan (other than a multiemployer plan) as an asset or liability in its statement of financial position and to recognize changes in that funded status in the year in which the changes occur through comprehensive income. FAS 158 is effective for financial statements as of December 31, 2006. The Company does not expect any material impact from applying FAS 158.

Note 2. Convertible Note Payable

On February 1, 2004, the Company executed a subscription agreement under which the Company issued to a corporation an 8% secured convertible note in exchange for $315,000. The note is due February 1, 2006, and is convertible into shares of the Company's common stock at the lower of $0.30 per share or 70% of the average of the three lowest trading prices for the 30 days prior to the conversion date. No beneficial conversion feature was applicable to this convertible note.

In April 2005, 285,832 common shares, in May 2005, 353,090 common shares and in May 2006, 529,279 common shares were issued in lieu of payment on this note and interest. The May 2006 payment of common stock repaid the balance owing on the note and all related interest.

Note 3. Discontinued Operations

In 2003, the Company signed the licensing agreement described in Note 1. This agreement changed the Company's business plan to that of a medical research company. Accordingly, the operating results related to the Company's research prior to the licensing agreement have been presented as discontinued operations in these financial statements for all periods presented.