Biocryst Pharmaceuticals Announces Publication Of Abstracts On Fodosine(TM) And Presentation At The 47th Annual Meeting And Exposition Of The American Society of Hematology
BIRMINGHAM, Ala., Nov. 17 /PRNewswire-FirstCall/ -- BioCryst Pharmaceuticals, Inc. today announced that three abstracts related to the clinical development of Fodosine(TM) (forodesine hydrochloride), its lead product candidate for the treatment of certain leukemias and lymphomas, have been published in the November 16, 2005 issue of Blood (Volume 106, Issue 11), the journal of the American Society of Hematology (ASH). The abstracts, which were prepared by clinical investigators and BioCryst staff, are available on the ASH website, www.hematology.org.
All three of the clinical studies described in the abstracts are scheduled for presentation at the upcoming ASH Annual Meeting, which will be held on December 10-13, 2005, in Atlanta, Georgia:
"Forodesine (Fodosine(TM)), a PNP Inhibitor Active in Relapsed or Refractory T-Cell Leukemia Patients (Phase II Study) (R. Furman et al.) will be presented by Dr. Richard R. Furman of Cornell University, during the Poster Session on Saturday, December 10 at 6:00 p.m. The poster includes an analysis of the Phase II trial data demonstrating that intravenous Fodosine(TM) is active with minimal toxicity, as a single agent in relapsed or refractory T-cell leukemia.
"Development of Forodesine Hydrochloride (FH), an Inhibitor of Purine Nucleoside Phosphorylase, for Patients with Chronic Lymphocytic Leukemia (CLL)" (K. Balakrishnan et al.), will be presented by Dr. Kumudha Balakrishnan of The University of Texas M.D. Anderson Cancer Center, during the Poster Session on Sunday, December 11 at 6:00 p.m. Dr. Balakrishnan will discuss results from a Phase II clinical study of Fodosine(TM), the first trial of a PNP inhibitor for the treatment of CLL.
"Phase I/II Study of Oral Fodosine(TM), a PNP Inhibitor in Refractory Cutaneous T-Cell Lymphoma Patients" (M. Duvic et al.) will be presented by Dr. Madeleine Duvic of The University of Texas M.D. Anderson Cancer Center, during the Poster Session on Sunday, December 11 at 6:00 p.m. Dr. Duvic will present data from the Phase I/II trial in which Fodosine(TM) showed preliminary evidence of clinical activity in refractory CTCL patients.
BioCryst Pharmaceuticals, Inc. designs, optimizes and develops novel drugs that block key enzymes involved in cancer, cardiovascular diseases, autoimmune diseases, and viral infections. BioCryst integrates the necessary disciplines of biology, crystallography, medicinal chemistry and computer modeling to effectively use structure-based drug design to discover and develop small molecule pharmaceuticals.
BioCryst's lead product candidate, Fodosine(TM), is a transition-state analog inhibitor of the target enzyme purine nucleoside phosphorylase (PNP). The drug is currently in a Phase IIa trial for patients with T-cell leukemia and a combination IV and oral Phase I pharmacokinetic trial in healthy volunteers. Results of the Phase IIa and the Phase I pharmacokinetic trial will assist in the design of a planned combination IV and oral Phase IIb pivotal clinical trial in patients with T-cell leukemia. The Company has requested a Special Protocol Assessment from the FDA for this planned trial. Additionally, Fodosine(TM) is currently being studied in a Phase I trial with an oral formulation in cutaneous T-cell lymphoma (CTCL) and a Phase II trial in chronic lymphocytic leukemia (CLL). BioCryst also plans to initiate a Phase I/II trial in B-cell acute lymphoblastic leukemia during 2005. Fodosine(TM) has been granted Orphan Drug status by the U.S. Food and Drug Administration for three indications: T-cell non-Hodgkin's lymphoma, including CTCL; CLL and related leukemias including T-cell prolymphocytic leukemia, adult T-cell leukemia, and hairy cell leukemia; and for treatment of B-cell acute lymphoblastic leukemia (ALL).
Additionally the FDA has granted "fast track" status to the development of Fodosine(TM) for the treatment of relapsed or refractory T-cell leukemia. A Phase Ib study with BioCryst's second-generation PNP inhibitor, BCX-4208, was recently initiated and is being conducted with the goal of initiating Phase II studies in patients with psoriasis in 2006. BioCryst has re-initiated clinical development of peramivir, an inhibitor of influenza neuraminidase, with a focus on intravenous and intramuscular delivery. Also, BioCryst has identified a clinical candidate, BCX-4678, in its hepatitis C polymerase inhibitor program, and is advancing this compound through preclinical testing with the goal of filing an IND in early 2006. For more information about BioCryst, please visit the company's web site at http://www.biocryst.com.
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. 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 that we may not be able to enroll the required number of subjects in clinical trials of Fodosine(TM) or BCX-4208, that each of the Phase IIa trial for patients with T-cell leukemia, Phase I trial of BCX-4208, the Phase I trial of Fodosine(TM) for treatment of patients with cutaneous T- cell lymphoma and the Phase II trial of Fodosine(TM) for advanced fludarabine- refractory CLL may not be successfully completed, that BioCryst may not commence as expected additional trials with Fodosine(TM) and with BCX-4208 or planned human trials with peramivir or BCX-4678, that Fodosine(TM), BCX-4208, peramivir, BCX-4678 or any of our other product candidates may not receive required regulatory clearances from the FDA, that Phase IIa clinical trials of Fodosine(TM) may not show the drug is effective over the 6-week period, that ongoing and future clinical trials may not have positive results, that we may not be able to obtain a Special Protocol Assessment or otherwise be able to complete successfully the Phase IIb trial that is currently planned to be pivotal, that we may not be able to continue future development of Fodosine(TM), BCX-4208, peramivir, BCX-4678 or any of our other current development programs including tissue factor/factor VIIa, that Fodosine(TM), BCX-4208, peramivir, BCX-4678 or our other development programs may never result in future product, license or royalty payments being received by BioCryst, that BioCryst may not reach favorable agreements with potential pharmaceutical and biotech partners for further development of its product candidates, that BioCryst may not have sufficient cash to continue funding the development, manufacturing, marketing or distribution of its products and that additional funding, if necessary, may not be available at all or on terms acceptable to BioCryst. 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, Quarterly Reports on Form 10-Q, current reports on Form 8-K and the latest Form S-3 which identify important factors that could cause the actual results to differ materially from those contained in the projections or forward-looking statements.
Contact: John Nugent of BioCryst Pharmaceuticals, Inc., 205-444-4633Photo: http://www.newscom.com/cgi-bin/prnh/20030414/BIOCRYSTLOGOAP Archive: http://photoarchive.ap.orgPRN Photo Desk, email@example.comBioCryst Pharmaceuticals, Inc.
CONTACT: John Nugent of BioCryst Pharmaceuticals, Inc., +1-205-444-4633