PVCT 10QSB 03-31-07
 



 
United States
Securities And Exchange Commission
Washington, DC 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 March 31, 2007

OR

o Transition Report under Section 13 or 15(d) of the Securities Exchange Act of 1934

For the transition period from __________ to _______________

Commission file number: 0-9410

Provectus Pharmaceuticals, Inc.
(Exact Name of Small Business Issuer as Specified in Its Charter)
 
 

 
Nevada
90-0031917
(State or other jurisdiction of incorporation or organization)
(I.R.S. Employer Identification Number)

7327 Oak Ridge Highway Suite A, Knoxville, TN 37931
(Address of Principal Executive Offices)

865/769-4011
(Issuer's Telephone Number, Including Area Code)

N/A
(Former Name, Former Address and Former Fiscal Year, if Changed Since Last Report)

Check whether the issuer: (1) filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 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 o
 
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act.     Yeso No x

The number of shares outstanding of the issuer's stock, $0.001 par value per share, as of April 24, 2007 was 45,450,619

Transitional Small Business Disclosure Format (check one): Yes o No   x

 



 




PROVECTUS PHARMACEUTICALS, INC.
(A Development-Stage Company)

CONSOLIDATED BALANCE SHEETS

 
   
March 31, 2007 
   
December 31, 2006
 
   
(Unaudited) 
   
(Audited)
 
               
Assets
             
               
Current Assets
             
Cash and cash equivalents
 
$
437,785
 
$
638,334
 
                United States Treasury Notes, total face value $7,037,755 and $6,507,019
   
7,029,645
   
6,499,034
 
Prepaid expenses and other current assets
   
162,019
   
173,693
 
               
Total Current Assets
   
7,629,449
   
7,311,061
 
               
Equipment and Furnishings, less accumulated depreciation of $375,035 and $372,721
   
49,888
   
30,075
 
Patents, net of amortization of $2,930,557 and $2,762,777
   
8,784,888
   
8,952,668
 
Deferred loan costs, net of amortization of $247,802 in 2006
   
--
   
3,713
 
Other assets
   
27,000
   
27,000
 
               
   
$
16,491,225
 
$
16,324,517
 
               
Liabilities and Stockholders' Equity
             
               
Current Liabilities
             
Accounts payable - trade
 
$
35,056
 
$
64,935
 
Accrued compensation
   
210,762
   
265,929
 
Accrued common stock costs
   
--
   
17,550
 
Accrued consulting expense
   
79,405
   
42,500
 
Other accrued expenses
   
29,500
   
46,500
 
March 2005 convertible debt, net of debt discount of $2,797 in 2006
   
--
   
364,703
 
               
Total Current Liabilities
   
354,723
   
802,117
 
               
Stockholders' Equity
             
Common stock; par value $.001 per share; 100,000,000 shares
authorized; 45,450,619 and 42,452,366 shares issued and
outstanding, respectively
   
45,451
   
42,452
 
Paid in capital
   
53,679,590
   
50,680,353
 
Deficit accumulated during the development stage
   
(37,588,539
)
 
(35,200,405
)
               
Total Stockholders' Equity
   
16,136,502
   
15,522,400
 
               
   
$
16,491,225
 
$
16,324,517
 

See accompanying notes to financial statements.

2

 
PROVECTUS PHARMACEUTICALS, INC.
(A Development-Stage Company)
CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited)

 
   
Three Months Ended
March 31, 2007 
   
Three Months Ended
March 31, 2006
   
Cumulative Amounts from January 17, 2002 (Inception) Through
March 31, 2007
 
Revenues
                   
               OTC product revenue
 
$
--
 
$
686
 
$
25,648
 
               Medical device revenue
   
--
   
--
   
14,109
 
                     
Total revenues
   
--
   
686
   
39,757
 
                     
Cost of Sales
   
--
   
439
   
15,216
 
                     
Gross profit
   
--
   
247
   
24,541
 
                     
Operating expenses
                   
               Research and development
 
$
1,089,303
 
$
450,510
 
$
8,217,510
 
               General and administrative
   
1,205,231
   
702,519
   
17,935,199
 
               Amortization
   
167,780
   
167,780
   
2,930,557
 
                     
Total operating loss
   
(2,462,314
)
 
(1,320,562
)
 
(29,058,725
)
                     
Gain on sale of fixed assets
   
--
   
--
   
55,075
 
                     
Loss on extinguishment of debt
   
--
   
--
   
(825,867
)
                     
Investment income
   
85,589
   
22,498
   
338,982
 
                     
Interest expense
   
(11,409
)
 
(1,002,179
)
 
(8,098,004
)
                     
Net loss
 
$
(2,388,134
)
$
(2,300,243
)
$
(37,588,539
)
                     
Basic and diluted loss per common share
 
$
(0.05
)
$
(0.07
)
     
                     
Weighted average number of common shares outstanding - basic and diluted
   
44,254,344
   
34,571,508
       
                     
                     

See accompanying notes to financial statements.

3

 
PROVECTUS PHARMACEUTICALS, INC.
(A Development-Stage Company)
CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY
(Unaudited)
 
Common Stock
     
 
Number of shares
Par value
Paid-in capital
Accumulated deficit
Total
Balance, at January 17, 2002
--
$ --
$ --
$ --
$ --
Issuance to founding shareholders
6,000,000
6,000
(6,000)
--
--
Sale of stock
50,000
50
24,950
--
25,000
Issuance of stock to employees
510,000
510
931,490
--
932,000
Issuance of stock for services
120,000
120
359,880
--
360,000
Net loss for the period from January 17, 2002 (inception) to April 23, 2002 (date of reverse merger)
--
--
--
(1,316,198)
(1,316,198)
Balance, at April 23, 2002
6,680,000
$ 6,680
$ 1,310,320
$ (1,316,198)
$ 802
Shares issued in reverse merger
265,763
266
(3,911)
--
(3,645)
Issuance of stock for services
1,900,000
1,900
5,142,100
--
5,144,000
Purchase and retirement of stock
(400,000)
(400)
(47,600)
--
(48,000)
Stock issued for acquisition of Valley Pharmaceuticals
500,007
500
12,225,820
--
12,226,320
Exercise of warrants
452,919
453
--
--
453
Warrants issued in connection with convertible debt
--
--
126,587
--
126,587
Stock and warrants issued for acquisition of Pure-ific
25,000
25
26,975
--
27,000
Net loss for the period from April 23, 2002 (date of reverse merger) to December 31, 2002
--
--
--
(5,749,937)
(5,749,937)
Balance, at December 31, 2002
9,423,689
$ 9,424
$18,780,291
$ (7,066,135)
$11,723,580
Issuance of stock for services
764,000
764
239,036
--
239,800
Issuance of warrants for services
--
--
145,479
--
145,479
Stock to be issued for services
--
--
281,500
--
281,500
Employee compensation from stock options
--
--
34,659
--
34,659
Issuance of stock pursuant to Regulation S
679,820
680
379,667
--
380,347
Beneficial conversion related to convertible debt
--
--
601,000
--
601,000
Net loss for the year ended December 31, 2003
--
--
--
(3,155,313)
(3,155,313)
Balance, at December 31, 2003
10,867,509
$ 10,868
$20,461,632
$ (10,221,448)
$10,251,052
Issuance of stock for services
733,872
734
449,190
--
449,923
Issuance of warrants for services
--
--
495,480
--
495,480
Exercise of warrants
132,608
133
4,867
--
5,000
Employee compensation from stock options
--
--
15,612
--
15,612
Issuance of stock pursuant to Regulation S
2,469,723
2,469
790,668
--
793,137
Issuance of stock pursuant to Regulation D
1,930,164
1,930
1,286,930
--
1,288,861
Beneficial conversion related to convertible debt
--
--
360,256
--
360,256
Issuance of convertible debt with warrants
--
--
105,250
--
105,250
Repurchase of beneficial conversion feature
--
--
(258,345)
--
(258,345)
Net loss for the year ended December 31, 2004
--
--
--
(4,344,525)
(4,344,525)
Balance, at December 31, 2004
16,133,876
$ 16,134
$23,711,540
$ (14,565,973)
$ 9,161,701
Issuance of stock for services
226,733
227
152,058
--
152,285
Issuance of stock for interest payable
263,721
264
195,767
--
196,031
Issuance of warrants for services
--
--
1,534,405
--
1,534,405
Issuance of warrants for contractual obligations
--
--
985,010
--
985,010
Exercise of warrants and stock options
1,571,849
1,572
1,438,223
--
1,439,795
Employee compensation from stock options
--
--
15,752
--
15,752
Issuance of stock pursuant to Regulation D
6,221,257
6,221
6,506,955
--
6,513,176
Debt conversion to common stock
3,405,541
3,405
3,045,957
--
3,049,795
Issuance of warrants with convertible debt
--
--
1,574,900
--
1,574,900
Beneficial conversion related to convertible debt
--
--
1,633,176
--
1,633,176
Beneficial conversion related to interest expense
--
--
39,259
--
39,529
Repurchase of beneficial conversion feature
--
--
(144,128)
--
(144,128)
Net loss for the year ended 2005
--
--
--
(11,763,853)
(11,763,853)
Balance, at December 31, 2005
27,822,977
$ 27,823
$40,689,144
$ (26,329,826)
$14,387,141
Issuance of stock for services
719,246
719
676,024
--
676,743
Issuance of stock for interest payable
194,327
195
183,401
--
183,596
Issuance of warrants for services
--
--
370,023
--
370,023
Exercise of warrants and stock options
1,245,809
1,246
1,188,570
--
1,189,816
Employee compensation from stock options
--
--
1,862,456
--
1,862,456
Issuance of stock pursuant to Regulation D
10,092,495
10,092
4,120,329
--
4,130,421
Debt conversion to common stock
2,377,512
2,377
1,573,959
--
1,576,336
Beneficial conversion related to interest expense
--
--
16,447
--
16,447
Net loss for the year ended 2006
--
--
--
(8,870,579)
(8,870,579)
Balance, at December 31, 2006
42,452,366
$ 42,452
$50,680,353
$ (35,200,405)
$15,522,400
Issuance of stock for interest payable
1,141
1
1,257
--
1,258
Issuance of warrants for services
--
--
75,933
--
75,933
Exercise of warrants and stock options
130,295
130
135,882
--
136,012
Employee compensation from stock options
--
--
573,395
--
573,395
Issuance of stock pursuant to Regulation D
2,376,817
2,378
1,845,760
--
1,848,138
Debt conversion to common stock
490,000
490
367,010
--
367,500
Net loss for the three months ended March 31, 2007
--
--
--
(2,388,134)
(2,388,134)
Balance, at March 31, 2007
45,450,619
$ 45,451
$53,679,590
$ (37,588,539)
$16,136,502
See accompanying notes to financial statements.
4



PROVECTUS PHARMACEUTICALS, INC.
(A Development-Stage Company)
CONSOLIDATED STATEMENTS OF CASH FLOW
(Unaudited)

   
Three Months Ended
March 31, 2007
 
Three Months Ended
March 31, 2006
 
Cumulative Amounts from January 17, 2002 (Inception) through
March 31, 2007
 
Cash Flows From Operating Activities
                   
Net loss
 
$
(2,388,134
)
$
(2,300,243
)
$
(37,588,539
)
Adjustments to reconcile net loss to net cash used in operating activities
                   
Depreciation
   
2,314
   
865
   
398,036
 
Amortization of patents
   
167,780
   
167,780
   
2,930,557
 
Amortization of original issue discount
   
2,797
   
657,800
   
3,845,721
 
Amortization of commitment fee
   
--
   
--
   
310,866
 
Amortization of prepaid consultant expense
   
42,010
   
--
   
1,253,217
 
Amortization of deferred loan costs
   
3,713
   
299,507
   
2,261,584
 
Accretion of United States Treasury Notes
   
(44,203
)
 
(22,498
)
 
(226,401
)
Loss on extinguishment of debt
   
--
   
--
   
825,867
 
Loss on exercise of warrants
   
--
   
--
   
236,146
 
Beneficial conversion of convertible interest
   
--
   
8,354
   
55,976
 
Convertible interest
   
1,258
   
38,249
   
389,950
 
Compensation through issuance of stock options
   
573,395
   
261,833
   
2,501,874
 
Compensation through issuance of stock
   
--
   
--
   
932,000
 
Issuance of stock for services
   
--
   
26,100
   
5,995,031
 
Issuance of warrants for services
   
75,933
   
--
   
619,102
 
Issuance of warrants for contractual obligations
   
--
   
--
   
985,010
 
Gain on sale of equipment
   
--
   
--
   
(55,075
)
(Increase) decrease in assets
                   
Prepaid expenses and other current assets
   
(30,336
)
 
(64,561
)
 
(120,010
)
Increase (decrease) in liabilities
                   
Accounts payable
   
(29,879
)
 
(72,849
)
 
31,411
 
Accrued expenses
   
(35,262
)
 
(107,472
)
 
497,964
 
                     
Net cash used in operating activities
   
(1,658,614
)
 
(1,107,135
)
 
(13,919,713
)
                     
Cash Flows from investing activities
                   
Proceeds from sale of fixed asset
   
--
   
--
   
180,075
 
Capital expenditures
   
(22,127
)
 
(8,601
)
 
(62,049
)
Proceeds from investments
   
5,000,000
   
--
   
16,000,000
 
Purchase of investments
   
(5,486,408
)
 
(2,468,752
)
 
(22,803,244
)
                     
Net cash used in investing activities
   
(508,535
)
 
(2,477,353
)
 
(6,685,218
)
                     
Cash Flows from Financing Activities
                   
Net proceeds from loans from stockholder
   
--
   
--
   
174,000
 
Proceeds from convertible debt
   
--
   
--
   
6,706,795
 
Net proceeds from sale of common stock
   
1,830,588
   
315,112
   
14,979,081
 
Proceeds from exercise of warrants and stock options
   
136,012
   
126,477
   
2,534,930
 
Cash paid to retire convertible debt
   
--
   
--
   
(2,385,959
)
Cash paid for deferred loan costs
   
--
   
--
   
(747,612
)
Premium paid on extinguishments of debt
   
--
   
--
   
(170,519
)
Purchase and retirement of common stock
   
--
   
--
   
(48,000
)
                     
Net cash provided by financing activities
   
1,966,600
   
441,589
   
21,042,716
 
                     
Net change in Cash and cash equivalents
 
$
(200,549
)
$
(3,142,899
)
$
437,785
 
                     
Cash and cash equivalents, at beginning of period
 
$
638,334
 
$
6,878,990
 
$
--
 
Cash and cash equivalents, at end of period
 
$
437,785
 
$
3,736,091
 
$
437,785
 
                     
 

 
Supplemental Disclosure of Noncash Investing and Financing activities:

March 31, 2007

1. Debt converted to common stock of $367,500
2. Payment of accrued interest through the issuance of stock of $1,258
3. Issuance of stock for stock issuance costs of $17,550 incurred in 2006

March 31, 2006

1. Debt converted to common stock of $750,000
2. Payment of accrued interest through the issuance of stock of $99,657
3. Issuance of stock for stock issuance costs of $964,676 incurred in 2005
4. Stock committed to be issued for services of $620,418 accrued at December 31, 2005 and issued in 2006


See accompanying notes to financial statements.

5


NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
(unaudited)

1. Basis of Presentation

The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with generally accepted accounting principles for interim financial information pursuant to Regulation S-B. Accordingly, they do not include all of the information and footnotes required by generally accepted accounting principles for complete financial statements. In the opinion of management, all adjustments (consisting of normal recurring accruals) considered necessary for a fair presentation have been included. Operating results for the three months ended March 31, 2007 are not necessarily indicative of the results that may be expected for the year ended December 31, 2007.

2. Recapitalization and Merger

Provectus Pharmaceuticals, Inc., formerly known as "Provectus Pharmaceutical, Inc." and "SPM Group, Inc.," was incorporated under Colorado law on May 1, 1978. SPM Group ceased operations in 1991, and became a development-stage company effective January 1, 1992, with the new corporate purpose of seeking out acquisitions of properties, businesses, or merger candidates, without limitation as to the nature of the business operations or geographic location of the acquisition candidate.

On April 1, 2002, SPM Group changed its name to "Provectus Pharmaceutical, Inc." and reincorporated in Nevada in preparation for a transaction with Provectus Pharmaceuticals, Inc., a privately-held Tennessee corporation ("PPI"). On April 23, 2002, an Agreement and Plan of Reorganization between Provectus Pharmaceutical and PPI was approved by the written consent of a majority of the outstanding shares of Provectus Pharmaceutical. As a result, Provectus Pharmaceuticals, Inc. issued 6,680,000 shares of common stock in exchange for all of the issued and outstanding shares of PPI. As part of the acquisition, Provectus Pharmaceutical changed its name to "Provectus Pharmaceuticals, Inc." and PPI became a wholly owned subsidiary of Provectus. This transaction was recorded as a recapitalization of PPI.

On November 19, 2002, the Company acquired Valley Pharmaceuticals, Inc., a privately-held Tennessee corporation formerly known as Photogen, Inc., by merging PPI with and into Valley and naming the surviving corporation "Xantech Pharmaceuticals, Inc." Photogen, Inc. was separated from Photogen Technologies, Inc. in a non-pro rata split-off to some of its shareholders. The assets of Photogen, Inc. consisted primarily of the equipment and intangibles related to its therapeutic activity and were recorded at their fair value. The majority shareholders of Valley were also the majority shareholders of Provectus. Valley had no revenues prior to the transaction with the Company. By acquiring Valley, the Company acquired its intellectual property, including issued U.S. patents and patentable inventions.

3. Basic and Diluted Loss Per Common Share

Basic and diluted loss per common share is computed based on the weighted average number of common shares outstanding. Loss per share excludes the impact of outstanding options, warrants, and convertible debt as they are antidilutive. Potential common shares excluded from the calculation at March 31, 2007 are 26,748,081 warrants, 8,884,419 options.

4. Equity and Debt Transactions

(a) In January 2007, the Company issued 150,000 shares committed to be issued at December 31, 2006 for shares sold in 2006. In January 2007, the Company issued 15,000 shares committed to be issued at December 31, 2006 for common stock costs related to shares sold in 2006. The total value for these shares was $17,550 which was based on the market value of the shares issued and was recorded as an accrued liability at December 31, 2006. In January and February 2007 the Company completed a private placement transaction with 6 accredited investors pursuant to which the Company sold a total of 265,000 shares of common stock at a purchase price of $1.00 per share, for an aggregate purchase price of $265,000. The Company paid $29,150 and issued 26,500 shares of common stock at a fair market value of $32,130 to Chicago Investment Group of Illinois, L.L.C. as a placement agent for this transaction. The cash costs have been off-set against the proceeds received. Also in January and February 2007 the Company completed a private placement transaction with 13 accredited investors pursuant to which the Company sold a total of 1,745,743 shares of common stock at a purchase price of $1.05 per share, for an aggregate purchase price of $1,833,031. The Company paid $238,293 and issued 174,574 shares of common stock at a fair market value of $200,760 to Network 1 Financial Securities, Inc. as placement agent for this transaction. The cash costs have been off-set against the proceeds received.

6

(b) In January 2007 the Company entered into a separate debt conversion agreement with two of its March 2005 accredited investors for $245,833 of convertible debt which was converted into 327,777 shares of common stock at $0.75 per share. In February 2007 the Company entered into a separate debt conversion agreement with two of its March 2005 accredited investors for $121,667 of convertible debt which was converted into 162,223 shares of common stock at $0.75 per share.

In February 2007, the remaining total debt discount has been amortized, which is $2,797. In February 2007 the remaining deferred loan costs have been amortized, which is $3,713.

At March 31, 2007 the Company had no remaining principal or accrued interest owed to holders of the March 2005 convertible debentures due on March 31, 2007.

The Company chose to pay a portion of the quarterly interest due at February 28, 2007 in common stock instead of cash. The accrued interest not paid in cash that was due February 28, 2007 of $1,109 was converted into 1,141 shares of common stock resulting in additional interest expense of $149. 358 of these shares were issued on January 25, 2007 and the remaining shares of 783 were issued on February 28, 2007.

(c) At March 31, 2007, $42,010 of prepaid consulting costs relating to warrants issued in 2006 have been charged to operations with the remaining $42,009 recorded as prepaid consulting expense as it represents payments for future services and the warrants are fully vested and non-forfeitable. During the three months ended March 31, 2007, the Company issued 85,000 warrants to consultants in exchange for services. Consulting costs charged to operations were $75,933.

5. Stock-Based Compensation

One employee of the Company exercised a total of 120,920 options during the three months ended March 31, 2007 at an exercise price of $1.10 per share of common stock for $133,012. Another employee of the Company exercised a total of 9,375 options during the three months ended March 31, 2007 at an exercise price of $0.32 per share of common stock for $3,000.

Effective January 1, 2006, the Company adopted FASB 123R. This change in accounting replaces existing requirements under FASB 123 and eliminates the ability to account for share-based compensation transaction using APB 25. The compensation cost relating to share-based payment transactions will be measured based on the fair value of the equity or liability instruments issued. For purposes of estimating the fair value of each stock option on the date of grant, the Company utilized the Black-Scholes option-pricing model. The Black-Scholes option valuation model was developed for use in estimating the fair value of traded options, which have no vesting restrictions and are fully transferable. In addition, option valuation models require the input of highly subjective assumptions including the expected volatility factor of the market price of the company’s common stock (as determined by reviewing its historical public market closing prices). Because the Company's employee stock options have characteristics significantly different from those of traded options and because changes in the subjective input assumptions can materially affect the fair value estimate, in management's opinion, the existing models do not necessarily provide a reliable single measure of the fair value of its employee stock options or restricted stock units. Included in the results for the three months ended March 31, 2007 and 2006, is $573,395 and $261,833, respectively, of stock-based compensation expense which relates to the fair value of stock options.

6. Cash Balance Defined Benefit Plan and Trust

In January 2007 the Company established the Provectus Pharmaceuticals, Inc. Cash Balance Defined Benefit Plan and Trust (the “Plan”), effective January 1, 2007, for the exclusive benefit of its four employees and their beneficiaries. The Plan was fully funded for 2007 in January totaling $324,000 or $81,000 per employee. The Plan contributions vest equally over six years and the Plan will be funded at approximately the same level each year in accordance with the provisions of the Plan.

Item 2. Management's Discussion and Analysis or Plan of Operation.

The following discussion is intended to assist in the understanding and assessment of significant changes and trends related to our results of operations and our financial condition together with our consolidated subsidiaries. This discussion and analysis should be read in conjunction with the consolidated financial statements and notes thereto included elsewhere in this Quarterly Report on Form 10-QSB. Historical results and percentage relationships set forth in the statement of operations, including trends which might appear, are not necessarily indicative of future operations.

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Capital Structure

Our ability to continue as a going concern is assured due to our financing completed during 2006. At the current rate of expenditures, we will not need to raise additional capital until 2008, although our existing funds are sufficient to meet anticipated needs throughout 2008.

We have implemented our integrated business plan, including execution of the current and next phases in clinical development of our pharmaceutical products and continued execution of research programs for new research initiatives.

We intend to proceed as rapidly as possible with the asset sale and licensure of our OTC products that can be sold with a minimum of regulatory compliance and with the further development of revenue sources through licensing of our existing medical device and biotech intellectual property portfolio. Although we believe that there is a reasonable basis for our expectation that we will become profitable due to the asset sale and licensure of our OTC products, we cannot assure you that we will be able to achieve, or maintain, a level of profitability sufficient to meet our operating expenses.

Our current plans include continuing to operate with our four employees during the immediate future, but we have added additional consultants and anticipate adding more consultants in the next 12 months. Our current plans also include minimal purchases of new property, plant and equipment, and increased research and development for additional clinical trials.

Plan of Operation

With the reorganization of Provectus and PPI and the acquisition and integration into the company of Valley and Pure-ific, we believe we have obtained a unique combination of OTC products and core intellectual properties. This combination represents the foundation for an operating company that we believe will provide both profitability and long-term growth. In 2007, we will carefully control expenditures in preparation for the asset sale and licensure or spin out of our OTC products, medical device and biotech technologies, and we will issue equity only when it makes sense to the company and primarily for purposes of attracting strategic investors.

In the short term, we intend to develop our business by selling the OTC assets and licensing our existing OTC products, principally Pure-Stick, GloveAid and Pure-ific. We are also now considering a spin out of the wholly owned subsidiary that contains the OTC assets. We will also sell and/or license our medical device and biotech technologies. In the longer term, we expect to continue the process of developing, testing and obtaining the approval of the U. S. Food and Drug Administration of prescription drugs in particular. Additionally, we have restarted our research programs that will identify additional conditions that our intellectual properties may be used to treat and additional treatments for those and other conditions.

Comparison of Three Months Ended March 31, 2007 and March 31, 2006.
 
Revenues

OTC Product Revenue decreased by $686 in the three months ended March 31, 2007 to $-0- from $686 in the three months ended March 31, 2006. We have discontinued our proof of concept program in November 2006 and have therefore ceased selling our OTC products.

Research and development

We have continued to make significant progress with the major research and development projects expected to be ongoing in the next 12 months. Our expanded Phase 1 metastatic melanoma clinical trial and the progress in our expanded Phase 1 breast carcinoma clinical trial was completed in April 2007 for approximately $1,000,000 in the aggregate, most of which has been expended in 2005 and 2006. The planning phase for the expected Phase 2 trial in metastatic melanoma has been completed which will cost approximately $3,000,000 through 2008. This includes expenditures in 2007 to significantly advance the proposed metastatic melanoma study which may provide pivotal efficacy. Additionally, we plan $1,000,000 of expenditures in 2007 to substantially advance our work with other oncology indications. Our Phase 2 psoriasis trial is expected to commence in June 2007 and will cost approximately $1,500,000 over 12 to 24 months. Our Phase 1 liver cancer trial is expected to cost approximately $500,000 in total, and is expected to commence in the third quarter of  2007.

Research and development costs of $1,089,303 for the three months ended March 31, 2007 included depreciation expense of $2,314, consulting and contract labor of $137,738, lab supplies and pharmaceutical preparations of $14,748, insurance of $19,568, legal of $52,830, payroll of $845,968, and rent and utilities of $16,137. Research and development costs of $450,510 for the three months ended March 31, 2006 included depreciation expense of $864, consulting and contract labor of $55,219, lab supplies and pharmaceutical preparations of $17,217, insurance of $8,208, legal of $44,622, payroll of $310,836, and rent and utilities of $13,544. The increase in consulting and contract labor is primarily the result of expense necessary to prepare for additional clinical trials expected to commence in the second quarter of 2007. The increase in payroll is the result of bonuses, pension expense, and the impact of adopting SFAS No. 123(R).

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General and administrative

General and administrative expenses increased by $502,712 in the three months ended March 31, 2007 to $1,205,231 from $702,519 for the three months ended March 31, 2006. The increase resulted primarily from higher payroll expenses for general corporate purposes as a result of bonuses, pension expense and the impact of adopting SFAS No. 123(R). Additionally, consulting expense increased $87,000 due to higher accounting expense and Sarbanes-Oxley Section 404 implementation expense.

Cash Flow

As of March 31, 2007, we held approximately $7,500,000 in cash and short-term United States Treasury Notes. At our current cash expenditure rate, this amount will be sufficient to meet our current and planned needs in 2007 and 2008. We have been increasing our expenditure rate by accelerating some of our research programs for new research initiatives; in addition, we are seeking to improve our cash flow through the asset sale and licensure of our OTC products. However, we cannot assure you that we will be successful in selling the OTC assets and licensing our existing OTC products. Moreover, even if we are successful in improving our current cash flow position, we nonetheless plan to require additional funds to meet our long-term needs in 2009 and beyond. We anticipate these funds will come from the proceeds of private placements, the exercise of existing warrants outstanding, or public offerings of debt or equity securities.

Capital Resources

As noted above, our present cash flow is currently sufficient to meet our short-term operating needs. Excess cash will be used to finance the current and next phases in clinical development of our pharmaceutical products. We anticipate that any required funds for our operating and development needs beyond 2008 will come from the proceeds of private placements, the exercise of existing warrants outstanding, or public offerings of debt or equity securities. While we believe that we have a reasonable basis for our expectation that we will be able to raise additional funds, we cannot assure you that we will be able to complete additional financing in a timely manner. In addition, any such financing may result in significant dilution to shareholders. For further information on funding sources, please see the notes to our financial statements included in this report.

Forward-Looking Statements

This Quarterly Report on Form 10-QSB contains forward-looking statements regarding, among other things, our anticipated financial and operating results. Forward-looking statements reflect our management’s current assumptions, beliefs, and expectations. Words such as "anticipate," "believe, “estimate," "expect," "intend," "plan," and similar expressions are intended to identify forward-looking statements. While we believe that the expectations reflected in our forward-looking statements are reasonable, we can give no assurance that such expectations will prove correct. Forward-looking statements are subject to risks and uncertainties that could cause our actual results to differ materially from the future results, performance, or achievements expressed in or implied by any forward-looking statement we make. Some of the relevant risks and uncertainties that could cause our actual performance to differ materially from the forward-looking statements contained in this report are discussed below under the heading "Risk Factors" and elsewhere in this Quarterly Report on Form 10-QSB. We caution investors that these discussions of important risks and uncertainties are not exclusive, and our business may be subject to other risks and uncertainties which are not detailed there.

Investors are cautioned not to place undue reliance on our forward-looking statements. We make forward-looking statements as of the date on which this Quarterly Report on Form 10-QSB is filed with the SEC, and we assume no obligation to update the forward-looking statements after the date hereof whether as a result of new information or events, changed circumstances, or otherwise, except as required by law.

Item 3. Controls and Procedures.

(a) Evaluation of Disclosure Controls and Procedures. Our chief executive officer and chief financial officer have evaluated the effectiveness of the design and operation of our "disclosure controls and procedures" (as that term is defined in Rule 13a-15(e) under the Exchange Act) as of March 31, 2007, the end of the fiscal quarter covered by this Quarterly Report on Form 10-QSB. Based on that evaluation, the chief executive officer and chief financial officer have concluded that our disclosure controls and procedures are effective to ensure that material information relating to the Company and the Company's consolidated subsidiaries is made known to such officers by others within these entities, particularly during the period this Quarterly Report on Form 10-QSB was prepared, in order to allow timely decisions regarding required disclosure.

(b) Changes in Internal Controls. There has been no change in our internal control over financial reporting that occurred during the fiscal quarter covered by this Quarterly Report on Form 10-QSB that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.

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PART II. OTHER INFORMATION

Item 1. Legal Proceedings.

The Company was not involved in any legal proceedings during the fiscal quarter covered by this Quarterly Report of Form 10-QSB.

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds.

Recent Sales of Unregistered Securities

In January and February 2007 the Company completed a private placement transaction with 6 accredited investors pursuant to which the Company sold a total of 265,000 shares of common stock at a purchase price of $1.00 per share, for an aggregate purchase price of $265,000. The Company paid $29,150 and issued 26,500 shares of common stock at a fair market value of $32,130 to Chicago Investment Group of Illinois, L.L.C. as a placement agent for this transaction. The cash costs have been off-set against the proceeds received. Also in January and February 2007 the Company completed a private placement transaction with 13 accredited investors pursuant to which the Company sold a total of 1,745,743 shares of common stock at a purchase price of $1.05 per share, for an aggregate purchase price of $1,833,031. The Company paid $238,293 and issued 174,574 shares of common stock at a fair market value of $200,760 to Network 1 Financial Securities, Inc. as placement agent for this transaction. The cash costs have been off-set against the proceeds received. The proceeds will be used for general corporate purposes.
 
Item 3. Defaults Upon Senior Securities.

None.

Item 4. Submission of Matters to a Vote of Security Holders.

None.

Item 5. Other Information.

None.

Item 6. Exhibits

31.1 Certification Pursuant to Rule 13a-14(a) (Section 302 Certification), dated May 11, 2007, executed by H. Craig Dees, Ph.D., Chief Executive Officer of the Company.

31.2 Certification Pursuant to Rule 13a-14(a) (Section 302 Certification), dated May 11, 2007, executed by Peter R. Culpepper, Chief Financial Officer of the Company.

32.1 Certification Pursuant to 18 U.S.C. ss. 1350 (Section 906 Certification), dated May 11, 2007, executed by H. Craig Dees, Ph.D., Chief Executive Officer of the Company, and Peter R. Culpepper, Chief Financial Officer of the Company.

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Signatures

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

                                                                                                                                                               Provectus Pharmaceuticals, Inc.
                                                                                                                                                               By:  /s/ H. Craig Dees, Ph.D.                      
                                                                                                                                                               H. Craig Dees, Ph.D. Chief Executive Officer

Date: May 11, 2007

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EXHIBIT INDEX

Exhibit
No.            Description
31.1          Certification Pursuant to Rule 13a-14(a) (Section 302 Certification), dated May 11, 2007, executed by H. Craig Dees, Ph.D., Chief Executive Officer of the Company.

31.2         Certification Pursuant to Rule 13a-14(a) (Section 302 Certification), dated May 11, 2007, executed by Peter R. Culpepper, Chief Financial Officer of the Company.

32.1         Certification Pursuant to 18 U.S.C. ss. 1350 (Section 906 Certification), dated May 11, 2007, executed by H. Craig Dees, Ph.D., Chief Executive Officer of the Company, and    Peter R. Culpepper, Chief Financial Officer of the Company.



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