108th CONGRESS
1st Session
H. R. 2968
To permit biomedical research corporations to engage in certain equity
financings without incurring limitations on net operating loss carryforwards
and certain built-in losses, and for other purposes.
IN THE HOUSE OF REPRESENTATIVES
July 25, 2003
Mr. REYNOLDS (for himself, Mr. CANTOR, Mr. MATSUI, Mr. CARDIN, and Mr. HOLT)
introduced the following bill; which was referred to the Committee on Ways
and Means
A BILL
To permit biomedical research corporations to engage in certain equity
financings without incurring limitations on net operating loss carryforwards
and certain built-in losses, and for other purposes.
Be it enacted by the Senate and House of Representatives of the United
States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the `Biotechnology Future Investment Expansion Act
of 2003'.
SEC. 2. FINDINGS AND PURPOSE.
(a) FINDINGS- Congress finds the following:
(1) American bioscience research corporations conduct long-term research
and development on breakthrough medical technologies. This commercial bioscience
research industry forms an irreplaceable link between pure scientific discovery
and the development of powerful biomedical products and technologies. It
is critical to the maintenance of American competitiveness internationally
that these long-term research and development projects be encouraged.
(2) Such long-term research projects have the greatest potential to revolutionize
whole fields of science and industry for the benefit of the standard of
living of Americans; and to yield solutions for critical social needs, even
though these solutions might not result in large sales and profits (such
as `orphan' drugs and other treatments alleviating great suffering in their
recipients).
(3) Long-term biomedical research companies are among the most research-intensive
and capital-intensive companies in the world.
(4) In addition to the scientific and technical risks attending their long-term
research programs, many biomedical research companies must subject their
technologies to lengthy and expensive regulatory reviews before they are
permitted access to the marketplace.
(5) Biomedical research companies typically operate in financially challenging
circumstances. These companies must engage in intensive research activity
for many years in order to develop their products and earn profits. Many
are small businesses lacking the internal cash flow, stability and borrowing
capacity of large corporations.
(6) The long-term commercial bioscience research industry is heavily dependent
on outside sources of equity capital to fund lengthy and intensive research
prior to earning any revenues. The industry's long lead times and high levels
of scientific and regulatory risk often impede access to capital.
(7) The longstanding national policy of Government support and tax incentives
for breakthrough commercial research reflects a recognition that the capital
marketplace tends to allocate insufficient resources to sustain the Nation's
need for such foundational scientific research and development.
(8) American long-term bioscience research companies constitute one of the
core commercial sectors which Congress intended to benefit from existing
tax incentives for commercial research.
(9) However, the current Federal income tax incentives are simply not working
in the case of many bioscience companies focused on breakthrough medical
technologies.
(10) Current Federal income tax incentives do not work as intended for most
high technology bioscience companies because they typically incur net operating
losses for a decade or more during their lengthy research and development
phases and therefore receive no contemporaneous benefit from these tax incentives.
(11) Further, Federal tax rules aimed chiefly at preventing corporate loss
trafficking and tax-motivated mergers and acquisitions penalize these companies.
The very process of raising successive increments of private capital through
routine equity financings triggers these rules and subjects biomedical research
companies to severe limitations on net operating loss and tax credit carryforwards.
These limitations practically eliminate for the commercial bioscience industry
any economic benefit from these tax incentives.
(12) These tax incentives instead tend to favor investment by large, profitable
companies, often engaged in secondary or tertiary research activities, and
thus to discriminate against and to cause under-investment in longer-term
breakthrough technologies, a bias which is harmful to American competitiveness.
(13) The inability to benefit from existing Federal income tax incentives
for commercial research places long-term bioscience research companies at
a substantial disadvantage in the capital marketplace where they must compete
with other companies able to use these tax incentives currently.
(14) A tax system that does not discriminate would ensure that existing
tax incentives in favor of research and experimentation have the same cost-reducing
impact on companies conducting both short-term and long-term research and
thus render this tax incentive program neutral with regard to short-term
and long-term research objectives, minimizing capital marketplace distortions
caused by differences in tax and income status.
(b) PURPOSE- The purpose of this Act is to provide that long-term biomedical
research corporations will not incur limitations on research-related tax incentive
carryforwards simply because they engage in the routine equity financings
that are the financial lifeblood of the industry.
SEC. 3. RESTORING THE BENEFIT OF TAX INCENTIVES FOR BIOMEDICAL RESEARCH
AND CLINICAL TRIALS.
(a) IN GENERAL- Subsection (l) of section 382 of the Internal Revenue Code
of 1986 is amended by adding at the end the following new paragraph:
`(9) CERTAIN FINANCING TRANSACTIONS OF BIOMEDICAL RESEARCH CORPORATIONS-
`(A) GENERAL RULE- In the case of a biomedical research corporation, any
owner shift involving a 5-percent shareholder which occurs as the result
of a qualified investment during the testing period shall be treated for
purposes of this section (other than this paragraph) as occurring before
the testing period.
`(B) BIOMEDICAL RESEARCH CORPORATION- For purposes of this paragraph,
the term `biomedical research corporation' means, with respect to any
qualified investment, any domestic corporation subject to tax under this
subchapter which is not in bankruptcy and which, as of the time of the
closing on such investment--
`(i) holds the rights to a drug or biologic for which an investigational
new drug application is in effect under section 505 of the Federal Food,
Drug, and Cosmetic Act, and
`(ii) certifies that, as of the time of such closing, the drug or biologic
is under study in phase II or phase III of a clinical investigation
carried out under such section.
`(C) QUALIFIED INVESTMENT- For purposes of this paragraph, the term `qualified
investment' means any acquisition of stock in a biomedical research corporation
if such stock is acquired at its original issue (directly or through an
underwriter), solely in exchange for cash, and the closing thereon occurs
after the date of the enactment of this paragraph.
`(D) STOCK ISSUED IN EXCHANGE FOR CONVERTIBLE DEBT- For purposes of this
paragraph, stock issued by a biomedical research corporation in exchange
for its convertible debt (or stock deemed under this section to be so
issued) shall be treated as stock acquired by the debt holder at its original
issue and solely in exchange for cash if the debt holder previously acquired
the convertible debt at its original issue and solely in exchange for
cash. In the case of an acquisition of stock in exchange for convertible
debt, the requirements of this paragraph shall be applied separately as
of the time of closing on the investment in convertible debt, and as of
the time of actual conversion (or deemed conversion under this section)
of the convertible debt for stock, except that the requirements of subparagraph
(H) shall be applied only as of the time of closing on the issuance of
the convertible debt.
`(E) BIOMEDICAL RESEARCH CORPORATION MUST MEET 5-YEAR EXPENDITURE TEST
WITH RESPECT TO ANY QUALIFIED INVESTMENT-
`(i) IN GENERAL- This paragraph shall not apply to a qualified investment
in a biomedical research corporation unless such corporation meets the
expenditure test for each year of the measuring period.
`(ii) MEASURING PERIOD- For purposes of this subparagraph, the term
`measuring period' means, with respect to any qualified investment,
the taxable year of the biomedical research corporation in which the
closing on the investment occurs, the 2 preceding taxable years, and
the 2 subsequent taxable years.
`(iii) EXPENDITURE TEST- A biomedical research corporation meets the
expenditure test of this subparagraph for a taxable year if at least
25 percent of its expenditures for the taxable year (including, for
purposes of this clause, payments in redemption of its stock) are expenditures
described in section 41(b) which are paid or incurred for clinical testing
or preclinical biomedical research.
`(iv) CLINICAL TESTING- For purposes of this subparagraph, the term
`clinical testing' means any human clinical testing which is carried
out under any investigational new drug application in effect under section
505 of the Federal Food, Drug, and Cosmetic Act.
`(F) EFFECT OF CORPORATE REDEMPTIONS ON QUALIFIED INVESTMENTS- Rules similar
to the rules of section 1202(c)(3) shall apply to qualified investments
under this paragraph except that `stock acquired in a qualified investment'
shall be substituted for `qualified small business stock' each place it
appears therein.
`(G) EFFECT OF OTHER TRANSACTIONS BETWEEN BIOMEDICAL RESEARCH CORPORATIONS
AND INVESTORS MAKING QUALIFIED INVESTMENTS-
`(i) IN GENERAL- If, during the 2-year period beginning 1 year before
any qualified investment, the biomedical research corporation engages
in another transaction with a member of its qualified investment group
and such biomedical research corporation receives any consideration
other than cash in such transaction, there shall be a presumption that
stock received in the otherwise qualified investment transaction was
not received solely in exchange for cash.
`(ii) QUALIFIED INVESTMENT GROUP- For purposes of this subparagraph,
the term `qualified investment group' means, with respect to any qualified
investment, one or more persons who receive stock issued in exchange
for the qualified investment, and any person related to such persons
within the meaning of section 267(b) or section 707(b).
`(iii) REGULATIONS- The Secretary shall promulgate regulations exempting
from this subparagraph transactions which are customary in the bioscience
research industry and are of minor value relative to the amount of the
qualified investment.
`(H) PROCEEDS OF QUALIFIED INVESTMENTS SHALL BE DEVOTED TO RESEARCH ON
PREEXISTING TECHNOLOGY-
`(i) IN GENERAL- This paragraph shall not apply to any qualified investment
unless the net proceeds of such qualified investment do not exceed the
excess of--
`(I) the sum of the biomedical research corporation's aggregate qualifying
clinical expenditures for the 3 years following the qualified investment,
over
`(II) three times the corporation's qualifying clinical expenditures
for the year preceding the qualified investment, plus the amount of
the corporation's cash and cash equivalents immediately before the
closing on the qualified investment.
`(ii) QUALIFYING CLINICAL EXPENDITURES- For purposes of this subparagraph,
the term `qualifying clinical expenditures' means amounts described
in section 41(b) which are paid or incurred by a biomedical research
corporation for clinical testing in connection with a drug or biologic
for which an investigational new drug application is in effect under
section 505 of the Federal Food, Drug, and Cosmetic Act and which is
(at the time of the closing on the qualified investment) under study
in phase II or phase III of a clinical investigation carried out under
such section.
`(I) REGULATIONS- The Secretary may issue such regulations as may be appropriate
to achieve the purposes of this paragraph, to prevent abuse, and to provide
for treatment of biomedical research corporations under sections 383 and
384 that is consistent with the purposes of this paragraph.'.
(b) PROCEEDS OF EQUITY INVESTMENTS TO BE TREATED AS WORKING CAPITAL- Subparagraph
(C) of section 382(l)(4) of such Code is amended by adding at the end the
following: `Such term shall not include any assets reasonably expected to
be used within 3 years to fund qualifying clinical expenditures (as defined
in paragraph (9)(H)(ii) without regard to the parenthetical therein).'.
(c) EFFECTIVE DATE- The amendments made by this section shall apply to taxable
years beginning after December 31, 2002.
END