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U.S. SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
_____________
FORM 10-Q
[ X ] QUARTERLY REPORT UNDER SECTION 13 OR 15 (d) OF THE SECURITIES EXCHANGE ACT
OF 1934
For the quarterly period ended March 31, 1999
or
[ ] TRANSITION REPORT UNDER SECTION 13 OR 15 (d) OF THE EXCHANGE ACT OF 1934
For the transition period from to
_____________
Commission file number 0-27914
RIBOZYME PHARMACEUTICALS, INC.
(Exact name of registrant as specified in its charter)
_____________
Delaware 34-1697351
(State of incorporation) (I.R.S. Employer Identification No.)
2950 Wilderness Place
Boulder, Colorado 80301
(Address of principal executive offices)
Registrant's telephone number: (303) 449-6500
_____________
Check whether the registrant: (1) has 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
----- -----
The number of shares of the registrant's common stock, par value $0.01 per
share, outstanding as of April 26, 1999 was 9,186,504.
RIBOZYME PHARMACEUTICALS, INC.
INDEX TO FORM 10-Q
PART 1 - FINANCIAL INFORMATION PAGE
----
Item 1. Financial Statements
Condensed Balance Sheets as of March 31, 1999 (unaudited) and
December 31, 1998............................................ 3
Condensed Statements of Operations - Three Months Ended
March 31, 1999 and 1998 (unaudited).......................... 4
Condensed Statements of Cash Flows - Three Months Ended
March 31, 1999 and 1998 (unaudited).......................... 5
Notes to Condensed Financial Statements (unaudited).......... 6
Item 2. Management's Discussion and Analysis of Financial
Condition and Results of Operations.......................... 7
Item 3. Quantitative and Qualitative Disclosures About Market Risk... 12
PART II - OTHER INFORMATION
Item 6. Exhibits and Reports on Form 8-K............................. 13
SIGNATURES............................................................ 14
Exhibit Index......................................................... 15
2
PART I. FINANCIAL INFORMATION
ITEM I. FINANCIAL STATEMENTS
RIBOZYME PHARMACEUTICALS, INC.
CONDENSED BALANCE SHEETS
ASSETS
------
March 31, December 31,
1999 1998
------------ ------------
(unaudited)
Current assets
- --------------
Cash and cash equivalents $ 4,805,279 $ 6,511,512
Securities available-for-sale 996,475
Accounts receivable 2,131,728 1,163,388
Accounts receivable-related parties 1,368,044 2,735,193
Prepaid expenses and other current assets 249,671 203,232
------------ ------------
Total current assets 9,551,197 10,613,325
Property, plant and equipment at cost,
net of accumulated depreciation 4,244,469 4,222,194
Notes receivable-related parties 138,000 162,466
Patent costs, net 2,926,696 2,905,575
Investment in Atugen Biotechnology GmbH 365,592 860,216
Other assets 457,590 460,515
------------ ------------
Total assets $ 17,683,544 $ 19,224,291
============ ============
LIABILITIES AND STOCKHOLDERS' EQUITY
------------------------------------
Current liabilities
- -------------------
Accounts payable-trade $ 1,527,816 $ 750,514
Accrued expenses 321,159 396,143
Deferred revenue, current portion-related parties 400,000 400,000
Current portion of long-term debt 442,512 498,179
------------ ------------
Total current liabilities 2,691,487 2,044,836
Deferred revenue, long-term portion-related parties 1,499,999 1,600,000
Long-term debt 160,254 200,455
Convertible debt-related parties 5,427,529 4,344,612
Stockholders' equity
- --------------------
Common stock 91,854 91,815
Additional paid-in capital 84,439,192 84,434,213
Deferred compensation and other (69,286) (69,149)
Accumulated deficit (76,557,485) (73,422,491)
------------ ------------
Total stockholders' equity 7,904,275 11,034,388
------------ ------------
Total liabilities and stockholders' equity $ 17,683,544 $ 19,224,291
============ ============
See notes to condensed financial statements
3
RIBOZYME PHARMACEUTICALS, INC.
CONDENSED STATEMENTS OF OPERATIONS
(Unaudited)
Three months ended
March 31,
----------------------
1999 1998
---- ----
Revenue
Collaborative agreements $ 1,701,235 $ 740,000
Other income 25,045
----------- -----------
Total revenues 1,701,235 765,045
Expenses
Research and development 3,760,433 5,000,870
General and administrative 559,296 467,205
----------- -----------
Total expenses 4,319,729 5,468,075
Operating loss (2,618,494) (4,703,030)
Other income (expense)
Interest income 90,215 212,329
Interest expense (112,091) (169,637)
Equity in loss of unconsolidated affiliate (494,624)
----------- -----------
Total other income (expense) (516,500) 42,692
Net loss $(3,134,994) $(4,660,338)
=========== ===========
Net loss per share $(0.34) $(0.54)
Shares used in computing net loss per share 9,182,095 8,608,740
=========== ===========
See notes to condensed financial statements
4
RIBOZYME PHARMACEUTICALS, INC.
CONDENSED STATEMENTS OF CASH FLOWS
(Unaudited)
Three months ended
March 31,
----------------------------
1999 1998
------------- -------------
Operating Activities
Net loss $(3,134,994) $(4,660,338)
Adjustments to reconcile net loss to
net cash used in operating activities:
Depreciation and amortization 416,649 450,025
Equity in loss of unconsolidated affiliate 494,624
Compensation for forgiveness of notes
receivable-related parties 52,466 52,466
Gain on sale of investment in corporate partner (25,045)
Accrued interest included in convertible debt 82,917 20,667
Changes in operating assets and liabilities:
Accounts receivable 398,809 544
Prepaid expenses and other current assets (39,438) 49,255
Other assets 2,925 (9,688)
Accounts payable-trade 777,301 700,285
Accrued expenses (74,984) (146,406)
Deferred revenue-related parties (100,001)
----------- -----------
Net cash used in operating activities (1,123,726) (3,568,235)
Investing activities
Additions to property, plant and equipment (413,124) (404,708)
Additions to deferred patent costs (46,921) (130,813)
Net purchases of securities available-for-sale (996,611) (1,008,710)
Sale of investment in corporate partner 275,045
Transfer of restricted cash 22,573
Loan repayments-related parties 1,875
Loan advances-related parties (35,000)
----------- -----------
Net cash used in investing activities (1,491,656) (1,244,738)
Financing activities
Net proceeds from sale of common stock 5,018 7,136
Payments under loan facilities (95,869) (334,662)
Borrowings under loan facilities 1,000,000 1,000,000
----------- -----------
Net cash provided by financing activities 909,149 672,474
Net decrease in cash and cash equivalents (1,706,233) (4,140,499)
Cash and cash equivalents at beginning of period 6,511,512 15,302,775
----------- -----------
Cash and cash equivalents at end of period $ 4,805,279 $11,162,276
=========== ===========
See notes to condensed financial statements.
5
RIBOZYME PHARMACEUTICALS, INC.
NOTES TO CONDENSED FINANCIAL STATEMENTS
March 31, 1999
(Unaudited)
Note 1: Basis of Presentation
The accompanying unaudited condensed financial statements have been
prepared in accordance with generally accepted accounting principles for interim
financial information and with the instructions to Form 10-Q and Article 10 of
Regulation S-X. 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-month period ending March 31,
1999 are not necessarily indicative of the results that may be expected for the
year ended December 31, 1999. For further information, refer to the financial
statements and footnotes thereto included in our annual report on Form 10-K/A
for the year ended December 31, 1998.
Note 2: Formation of Atugen, GmbH
In December 1998, we transferred our gene function and target
validation business and technology to Atugen Biotechnology, GmbH, a newly formed
German corporation. Financing for Atugen GmbH was accomplished through
investments and commitments of approximately $20 million, including an equity
investment of $2.0 million from us, a venture capital investment of $7.0 million
and a commitment by German government agencies to provide grants and loans
of up to $10.0 million. As a result, at December 31, 1998, we retained a 49.5%
ownership in Atugen GmbH. In connection with its formation, Atugen GmbH received
exclusive royalty free licenses to our patents and technologies for target
validation and discovery in exchange for a one-time $2.0 million payment which
we received in January 1999. We have deferred the $2.0 million license payment
and will recognize it ratably over the five year term of the license agreement.
Atugen GmbH has deferred the entire amount of this one-time payment as of
December 31, 1998 and will amortize the expense over the five year term of the
license agreement. Atugen GmbH's expense of the license agreement will be
reflected in our equity in earnings or loss of this unconsolidated affiliate.
According to a service agreement executed by both parties, we will
provide management support, technologies, facilities and reagents to Atugen for
reasonable fees. We will retain rights to develop oligonucleotide therapeutic
agents against targets validated by Atugen.
Note 3: Collaboration with Eli Lilly and Company
In March 1999, we entered into a collaboration with Eli Lilly and
Company to conduct research, development and commercialization of HEPTAZYME,
our ribozyme for the treatment of Hepatitis C virus infection. Under the terms
of the agreement, we will receive approximately $1.7 million in 1999 in research
revenues to fund research and other RPI expenses. In addition, in April
1999, Lilly purchased five shares of our Series L preferred stock for $7.5
million. We may receive success fees related to various development milestones
and royalties on future sales of products developed related to the
collaboration. Lilly will receive the exclusive worldwide commercialization
rights to products that result from this collaboration, including the HEPTAZYME
product. We have retained certain rights to manufacture HEPTAZYME products
resulting from the collaboration.
6
ITEM 2. MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND
RESULTS OF OPERATIONS.
Overview of our Business
Ribozyme Pharmaceuticals was founded to develop commercial products and
services based upon the significant potential of "ribozymes," a discovery of
Professor Thomas R. Cech for which he shared a Nobel Prize. Our primary
business focus is to use our technology to develop a new class of drugs
consisting of ribozymes to treat or prevent human disease. We are in various
stages of clinical trials and preclinical development for two lead product
candidates: ANGIOZYME for the treatment of solid tumor cancers and HEPTAZYME for
the treatment of Hepatitis C. Chiron Corporation is our collaborator for the
development and commercialization of ANGIOZYME and Eli Lilly and Company is our
collaborator for the development and commercialization of HEPTAZYME. We have
gene function identification and target validation agreements with Schering AG,
Roche Bioscience and GlaxoWellcome. In addition, we have existing gene function
identification and target validation agreements with Chiron and Parke-Davis
which are substantially complete, but we may be obligated to perform additional
work.
We recently completed Phase Ia clinical trials in normal volunteers for
our most advanced product candidate, ANGIOZYME. We began Phase Ib trials in
cancer patients in the first quarter of 1999 and expect to commence Phase II
trials before the end of 1999. We expect to file an IND for our second product
candidate, HEPTAZYME, in the fourth quarter of 1999 and commence clinical trials
in 2000. To date, we have committed substantially all our resources to our
research and product development programs. We have not generated any revenues
from product sales, nor do we anticipate any in the foreseeable future. Our
revenues consist primarily of research payments and milestones from our
collaborators. We depend upon funding from external financing and corporate
collaborations for our research and product development programs and expect to
do so for the foreseeable future.
We expect to commit significant additional resources conducting these
clinical trials for ANGIOZYME, as well as for clinical trials for other
potential product candidates. In addition, although we believe our existing
manufacturing facilities and those available from contract manufacturers will be
satisfactory for the manufacture of our current product candidates through
clinical trials, we will need to commit significant resources in order to
support manufacture on a commercial scale.
We have not been profitable since inception and have an accumulated
deficit of $76.6 million as of March 31, 1999. Losses have resulted primarily
from our research and development programs. We anticipate incurring additional
losses as ANGIOZYME and HEPTAZYME advance through clinical development. In
addition, future milestone payments under some of our collaborations are
contingent upon our meeting particular research or development goals. The amount
and timing of future milestone payments are contingent upon the terms of each
agreement. Milestone performance criteria is specific to each agreement and
based on our future performance. In some instances, milestone payments may be
forfeited if a goal is not accomplished within a certain time frame. Therefore,
we are subject to significant variation in the timing and amount of our revenues
and results of operations from period to period.
In 1998, we announced the formation of a new company, Atugen
Biotechnology GmbH, in Berlin, Germany that utilizes our proprietary ribozyme
and related technologies as a continuation of our target validation and
discovery business. The formation of Atugen GmbH took place through private
7
sector investments and funding commitments from the German government as part of
its initiative to encourage new biotechnology investments in Germany. In 1998,
we transferred our gene identification and target validation technology to
Atugen GmbH in exchange for a substantial equity interest. We plan to have an
on-going business relationship with Atugen GmbH.
We expect to continue our existing gene identification and target
validation agreements with our collaborators by subcontracting services to
Atugen GmbH. Atugen GmbH will enter into future gene identification and target
validation agreements directly with collaborators, but we will retain rights to
use the technology internally, and develop oligonucleotides as therapeutic
agents against all targets validated by Atugen GmbH. In 1998, we received a one-
time license fee from Atugen GmbH for the exclusive rights to our gene
identification and target validation technology. In our on-going relationship
with Atugen GmbH, we will receive payments for:
* management and administrative services we provide,
* oligonucleotides and other chemicals, and
* prosecution of relevant patents.
In addition, we will retain exclusive manufacturing rights to oligonucleotide
therapeutic agents resulting from validation services. Atugen GmbH will be
reimbursed for any subcontracting services it provides to us on a full time
equivalent basis.
Results of Operations
Three Months Ended March 31, 1999 and 1998
Collaborative revenues increased to $1.7 million for the three months
ended March 31, 1999, from $740,000 for the corresponding period in 1998. The
increase is primarily due to $1.1 million in revenues recorded from Chiron
related to joint product development of ANGIOZYME. According to the Chiron
agreement, Chiron and RPI share equally in the clinical trial costs of
ANGIOZYME, and for the first quarter of 1999, RPI incurred virtually all
expenses related to ANGIOZYME. Revenue recorded from Chiron is for research and
development expenses already incurred and no further obligation exists between
us and Chiron related to revenues recognized. Future Chiron revenues related to
the joint development of ANGIOZYME will be variable and depend on the stage of
ANGIOZYME clinical development. In addition, during the first quarter of 1999,
$593,000 in revenue was recorded in connection with our the service agreement
with Atugen GmbH. Atugen GmbH pays for reagents and management and
administrative services we provide. Atugen Gmbh revenues are earned as the
products and services are provided. Future revenues will depend on the level of
activities performed by us for Atugen Gmbh. Generally, revenue fluctuations
result from changes in the number of funded research projects as well as the
timing and completion of contract milestones.
In January 1998, we recorded as other income a gain of $25,000 from the
sale of stock in a privately held corporate partner back to that corporate
partner. We purchased this stock in the first quarter of 1996 for $250,000.
Research and development expenses decreased to $3.8 million for the
three months ended March 31, 1999, compared to $5.0 million for the
corresponding period in 1998. The decrease was primarily due to transferring our
gene identification and target validation business to Atugen GmbH. In January
1999, Atugen USA, a wholly-owned subsidiary of Atugen GmbH, was incorporated and
subsequently all
8
gene identification and target validation expenses previously charged to us were
transferred to Atugen USA. Expenses of approximately $797,000 were recorded by
Atugen USA during the first quarter of 1999, which included payroll, facility
and general expenses for approximately fifteen employees transferred to Atugen
USA. Expenses for the approximately fifteen employees transferred to Atugen USA
were included in our 1998 first quarter amount, but were not included in the
1999 amount. However, we expect research and development expenses to increase as
we expand our development programs for ANGIOZYME and HEPTAZYME, including pre-
clinical studies and clinical trials.
General and administrative expenses increased to $559,000, for the
three months ended March 31, 1999, compared to $467,000 for the corresponding
period in 1998. The increase is primarily the result of increased staffing and
associated expenses necessary to manage and support our expanding product and
business development efforts. We expect general and administrative expenses to
continue to increase as a result of increasing legal and other professional fees
in connection with the overall scale-up of our operations, business development
efforts and patent protection.
Interest income has decreased to $90,000 for the three months ended
March 31, 1999 compared to $212,000 for the corresponding period in 1998. The
decrease is due to lower average balances in our cash and cash equivalents and
securities available-for-sale during the first quarter of 1999, as compared to
the same quarter in 1998. Interest income generally fluctuates as a result of
the average amount of cash available for investment and prevailing interest
rates.
Interest expense decreased to $112,000 for the three months ended March
31, 1999 compared to $170,000 for the corresponding period in 1998. The
decrease is due to the payoff of a loan for tenant improvements and equipment in
December 1998. However, interest expense is expected to increase as we arrange
for additional financing for future operation of our business.
Equity in loss of unconsolidated affiliate was $495,000 for the period
ending March 31, 1999. No expense was required or recorded in the corresponding
period in 1998. The expense is in connection with our initial cash investment
of $2.0 million and the subsequent transfer of our gene identification and
target validation technology to Atugen GmbH in 1998. At March 31, 1999, we
owned 83.2% of Atugen GmbH's outstanding common stock and, as a result, we
recorded our share of Atugen GmbH's first quarter net loss of $595,000,
resulting in equity in loss of unconsolidated affiliate of $495,000. At March
31, 1999, our remaining net investment in Atugen GmbH was $366,000, which we
expect to eliminate entirely during the remainder of 1999 as we share further in
Atugen GmbH's anticipated losses.
Liquidity and Capital Resources
We have financed our operations since inception through public
offerings in April 1996 and October 1997, private placements of preferred stock,
loans from financial institutions and funds received under our collaborative
agreements with a number of corporate partners. From inception through March 31,
1999, we have received approximately:
* $29.0 million in net proceeds from private placements,
* $31.1 million in net proceeds from public offerings,
* $41.9 million from our collaborations, and
* $9.8 million in equipment financing.
We had cash, cash equivalents and securities available-for-sale of
$5.8 million at March 31, 1999, compared to $6.5 million at December 31, 1998.
The $700,000 decrease in cash, cash equivalents
9
and securities available-for-sale is primarily the result of $1.1 million used
for operations, $460,000 used for investments in equipment and patents, and
$140,000 in loan payments, loan advances and expenses related to a stock
offering, offset by loan proceeds of $1.0 million.
We invest our cash, cash equivalents and securities available-for-sale
in interest-bearing investment grade securities.
Schering AG made a $2.5 million equity investment in us in May 1997 in
exchange for 212,766 shares of common stock and made an additional equity
investment of $2.5 million for 465,117 shares in April 1998. Separately,
Schering AG provided loans of $2.0 million in each of 1997 and 1998. In
addition, we received $1.0 million on this loan facility in January 1999.
Schering AG will continue to provide loans of up to $2.0 million annually for
each of the next three years, provided that the collaboration is continued, at
Schering AG's option, in each of those years. Amounts not used in any calendar
year may be carried forward to future years. According to the terms of our
agreement with Schering AG, 50% of any borrowings on the line of credit must be
collateralized by equipment purchases. The loans, which carry an interest rate
of 8.0% per annum, are immediately convertible into equity at the option of
Schering AG. At March 31, 1999, the outstanding borrowings of $5.4 million were
convertible into approximately 1.1 million shares of our common stock.
Principal and interest payments are deferred until maturity of the loans which
is April 2004. In addition, Schering AG made research payments of $500,000,
$2.0 million and $1.5 million in 1999, 1998 and 1997, respectively. If the
collaboration is continued, Schering AG will make research payments of $2.0
million a year for each year through April 2002. We may earn success fees upon
product development milestones and will manufacture synthetic ribozyme products
and receive royalties on sales of products resulting from the collaboration.
Schering AG may terminate the research collaboration at any time by paying us
termination fees.
In March 1999, we entered into a collaboration with Eli Lilly and
Company pursuant to which Lilly was granted the exclusive worldwide right to
develop and commercialize HEPTAZYME and any other ribozyme drug for the
treatment of Hepatitis C infection. If Lilly abandons or does not diligently
pursue the development of HEPTAZYME or another ribozyme drug for the treatment
of Hepatitis C infection, all rights to HEPTAZYME and such other ribozymes
revert to us, subject to the right of Lilly to receive royalty payments, if
applicable, on the sale of products developed by us or our third-party
collaborators.
Lilly will pay us $9.2 million in 1999, which includes:
* $1.7 million for funding for research and clinical trial materials,
and
* $7.5 million equity investment.
Including development milestones, which we will be entitled to receive if a
commercial product is offered for sale in the United States, Europe and Japan,
we could receive as much as $38 million including the $9.2 million set forth
above. In addition we will be entitled to royalties on the sale of products
developed pursuant to the collaborations. We could also realize increased
revenues from product manufacturing and research.
Total additions for property, plant and equipment for the three months
ended March 31, 1999 were $413,000, all of which were financed through our
existing loan facility from Schering AG.
10
We anticipate that our existing financial resources, the equity
investment from Lilly, expected revenues from our collaborations and the
estimated proceeds of expected offerings should be adequate to satisfy our
anticipated capital requirements through 2001. We expect to incur substantial
additional research and development costs, including costs related to:
* our research, drug discovery and development programs,
* preclinical and clinical trials of our products, if developed,
* our acquisition of interests in products or services currently held
by third parties,
* prosecuting and enforcing patent claims,
* general administrative and legal items, and
* manufacturing and marketing of products, if any.
We may raise additional capital through public or private financing,
as well as collaborative relationships, borrowings and other available sources.
We cannot assure you that funds will be available on favorable terms, if at all.
If we raise additional funds by issuing equity securities, the holdings of
existing stockholders will be further diluted. In addition, future
collaborative relationships may not successfully reduce our funding requirements
which may require us to relinquish or reduce rights to our technologies or
products.
Year 2000 Affect on Computer Systems
Year 2000 issues result from the inability of some computer programs
or computerized equipment to accurately calculate, store or use a date
subsequent to December 31, 1999. The erroneous date can be interpreted in a
number of different ways; typically the year 2000 is represented as the year
1900. This could result in a system failure or miscalculations causing
disruptions of operations, including, among other things, a temporary inability
to process transactions, send invoices or engage in similar normal business.
Based on our evaluations and remediation efforts, we do not anticipate
that we will incur any significant costs relating to the assessment and
remediation of year 2000 issues. To date, we estimate that we have spent
approximately $20,000 in reviewing and remediating year 2000 issues and that
total expenditures incurred in completing our review and remediation efforts
will not exceed $60,000. These expenditures are budgeted as part of our
operating expenses. However, expenditures for year 2000 remediation efforts may
exceed this amount if unforeseen complications arise. Also, we or our vendors,
suppliers and corporate partners may not be able to successfully identify and
remedy all potential year 2000 problems.
We have developed and are implementing a contingency plan including the
following:
* maintaining all data in hard copy that is generated or collected by
our vendors, suppliers and collaborators so any loss of data due to
year 2000 problems could be re-entered manually,
* maintaining all of our accounting records in hard copy so that we
can continue to manually pay vendors, employees, consultants and
collaborators in the event that our accounting software or other
computer programs or systems malfunction,
* maintaining hard copies of all scientific and business related
electronic data,
* archiving critical business paperwork,
* scheduling manufacturing campaigns not to extend or overlap the year
2000 time change, and
* upgrading security systems.
11
We are continuing to review these requirements in order to complete
our contingency plan for noncritical business functions.
We do not believe that we will have to modify or replace any
significant portions of our computer applications in order for our computer
systems to continue to function properly in the year 2000. However, a "worst
case" scenario may include the temporary interruption of research, development
and business if we need to upgrade or replace computer systems.
Statements in this Form 10-Q which are not strictly historical are
"forward-looking" statements which should be considered as subject to the many
uncertainties that exist in our operations and business environment. These
uncertainties, which include, among other things, the following: general
economic and business conditions; competition; technological advances; ability
to obtain rights to technology; ability to obtain and enforce patents; ability
to commercialize and manufacture products; ability to obtain collaborators;
ability to manufacture ribozymes in adequate amounts for its collaborations and
clinical trials; results of clinical studies; results of research and
development activities; business abilities and judgment of personnel;
availability of qualified personnel; changes in, or failure to comply with,
governmental regulations; ability to obtain adequate financing in the future;
and the like, are set forth in our 10-K/A for the year ended December 31, 1998
which is on file with the U.S. Securities and Exchange Commission, a copy of
which is available from us.
ITEM 3. QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
Not applicable.
12
PART II - OTHER INFORMATION
ITEM 6. EXHIBITS AND REPORTS ON FORM 8-K
(a) Exhibits
3(i) Amended and Restated Certificate of Incorporation (1)
3(ii) Restated Bylaws (2)
27 Financial Data Schedule
(b) Reports on Form 8-K
The Company filed a report on Form 8-K, dated March 19, 1999, which
reported a Participation Agreement, as amended, dated August 31, 1998,
and related documents between Ribozyme Pharmaceuticals, Inc. and
Atugen Biotechnology, GmbH.
______
(1) Incorporated by reference from the Company's Registration Statement on Form
SB-2, file no. 333-34981, dated September 5, 1997.
(2) Incorporated by reference from the Company's Registration Statement on Form
SB-2, file no. 333-1908-D, dated April 11, 1996.
13
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.
RIBOZYME PHARMACEUTICALS, INC.
Dated: May 6, 1999 By: /s/ RALPH E. CHRISTOFFERSEN
----------- ----------------------------
Ralph E. Christoffersen
President and Chief
Executive Officer
Dated: May 6, 1999 By: /s/ LAWRENCE E. BULLOCK
----------- -----------------------
Lawrence E. Bullock
Vice President and Chief Financial Officer
(Principal Financial Officer and
Principal Accounting Officer)
14
Exhibit Index
Exhibit Exhibit
No. Description
- ------------ -----------------------------------------------------
3(i) Amended and Restated Certificate of Incorporation (1)
3(ii) Restated Bylaws (2)
27 Financial Data Schedule
_____
(1) Incorporated by reference from the Company's Registration Statement on Form
SB-2, file no. 333-34981, dated September 5, 1997.
(2) Incorporated by reference from the Company's Registration Statement on Form
SB-2, file no. 333-1908-D, dated April 11, 1996.
15