BIOCRYST REPORTS FIRST QUARTER 2001 FINANCIAL RESULTS
Revenues increased in the first quarter of 2001 over the same period last year primarily as a result of the timing of the receipt of milestone payments from The R.W. Johnson Pharmaceutical Research Institute (RWJPRI) and related recognition of the revenue after the adoption of SAB 101. Research and development expenses increased 30.7% to $2.5 million in the three months ended March 31, 2001 from $1.9 million in the three months ended March 31, 2000. The increase is primarily attributable to an increase in facilities expenses and related personnel increases resulting from the expansion of our facility and staff during 2000. General and administrative expenses decreased 32.0% during the same period primarily due to a reduction in legal fees and the reduced Alabama share tax assessment in 2001.
The Company will conduct a conference call, which is open to the public, at 10:00 am EDT on Wednesday, April 25. The conference call dial-in number is 1-800-289-0496, and the passcode number is 440430. The conference call will also be available by webcast on the Company's investor relations website, www.biocryst.com.
Founded in 1986, BioCryst Pharmaceuticals, Inc. is a biopharmaceutical company focused on the development of pharmaceuticals for the treatment of viral, inflammatory/autoimmune and cardiovascular diseases and disorders. BioCryst's most advanced drug candidate, RWJ-270201 (formerly known as BCX-1812), is a neuraminidase inhibitor designed to treat and prevent viral influenza. The Company licensed this drug candidate to The R.W. Johnson Pharmaceutical Research Institute and Ortho-McNeil Pharmaceutical, Inc., both Johnson & Johnson companies.
These statements involve known and unknown risks, uncertainties and other factors which may cause our actual results, performance or achievements to be materially different from any future results, performances or achievements expressed or implied by the forward-looking statements. Forward-looking statements include, but are not limited to The R.W. Johnson Pharmaceutical Research Institute (RWJPRI) and Ortho-McNeil Pharmaceutical, Inc.'s progress with respect to our influenza neuraminidase inhibitors and developments with respect to clinical trials and the regulatory approval process. These statements reflect our current views with respect to future events and are based on assumptions and subject to risks and uncertainties. Given these uncertainties, you should not place undue reliance on these forward-looking statements. Some of the factors that could affect the forward-looking statements contained herein include, without limitation that any Phase III clinical trials may not be successful or be pivotal in nature, that an NDA might not be filed, or that our license with RWJPRI and Ortho-McNeil might be terminated. Even if RWJPRI completes the Phase III clinical trials, we do not know when, if ever, it will receive FDA or foreign regulatory agency approvals for, or when Ortho-McNeil will begin marketing of RWJ-270201. Please refer to the documents BioCryst files periodically with the Securities and Exchange Commission, specifically BioCryst's most recent Annual report on Form 10-K, which identifies important factors that could cause the actual results to differ materially from those contained in the forward-looking statements.