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MedImmune's Advancing Cancer Pipeline To Be Highlighted At The American Society Of Hematology's Annual Meeting
Article Date: 11 Dec 2006 - 0:00am (PST)
MedImmune, Inc. (Nasdaq: MEDI) announced today that results from three programs within the company's expanding oncology pipeline will be presented at the American Society of Hematology (ASH) 48th Annual Meeting, held December 9-12, 2006 in Orlando, FL. Clinical program updates include interim data for potential cancer therapies targeting multiple myeloma and certain leukemias and lymphomas.
"MedImmune continues to affirm its commitment to oncology as a vital therapeutic area by advancing and expanding its pipeline of product candidates targeting various cancers, signified by ASH's acceptance of seven scientific presentations by MedImmune and its partners," commented Dirk Reitsma, M.D., MedImmune's vice president, clinical development, oncology.
Data to be presented at ASH include:
-- "Update on Phase 1 Clinical Trial of IPI-504, a Novel, Water-Soluble Hsp90 Inhibitor, in Patients with Relapsed/Refractory Multiple Myeloma" (Abstract 3579, presented in a poster session, "Myeloma: Novel Agents and Toxicities," on Monday, Dec. 11 at 10:30 a.m.)
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-- "A Phase 1 Open Label Dose Escalation Study To Evaluate MEDI-507 in Patients with CD2-Positive T-Cell Lymphoma/Leukemia" (Abstract 2727, presented in a poster session, "Novel and Targeted Therapy of NHL," on Sunday, Dec. 10 at 9 a.m.)
-- "The Bi-Specific T-Cell Enhancer (BiTE) MT103 (MEDI-538) Induces Clinical Responses in Heavily Pre-Treated NHL Patients: Update from the Ongoing Phase 1 Study MT103-104" (Abstract 693, presented in an oral session, "Targeted Therapy of NHL," on Monday, Dec. 11 at 4 p.m.)
-- "Hsp90 Inhibition Decreases Survival of BCR-ABL T315I Leukemic Stem Cells in Mice" (Abstract 2184, presented in a poster session, "Chronic Myeloid Leukemia: New Drugs," on Sunday, Dec. 10 at 9 a.m.)
-- "IPI-504, a Novel, Orally Active Hsp90 Inhibitor, Prolongs Survival of Mice with BCR-ABL T315I CML and B-ALL" (Abstract 2183, presented in a poster session, "Chronic Myeloid Leukemia: New Drugs," on Sunday, Dec. 10 at 9 a.m.)
-- "T Cell Responses During Long-Term Continuous Infusion of MT-103 (MEDI- 538; Anti-CD19 BiTE) In Patients with Relapsed B-NHL: Data from Dose- Escalation Study MT103-104" (Abstract 2725, presented in a poster session, "Novel and Targeted Therapy of NHL," on Sunday, Dec. 10 at 9 a.m.)
-- "Mechanistic Evaluation of Siplizumab (MEDI-507) Activity On Normal and Malignant T-Lymphocytes" (Abstract 2504, presented in a poster session, "Lymphoma: Pre-Clinical -- Chemotherapy and Biologic Agents," on Sunday, Dec. 10 at 9 a.m.)
All abstracts presented at the ASH meeting were published in Blood, Volume 108, Issue 11 on November 16, 2006.
About Hsp90 and IPI-504
IPI-504 is a proprietary small molecule therapeutic drug candidate currently being evaluated as part of a drug development and worldwide commercialization agreement between MedImmune and Infinity Pharmaceuticals, Inc. In preclinical studies, IPI-504 has potently and selectively inhibited Hsp90, thereby killing cancer cells. Hsp90 is an emerging therapeutic target of interest for the treatment of cancer. Proteins are the mainstay of structural and signaling elements of all cells. Hsp90 functions to stabilize and maintain the activity of proteins in the cancer cell, thereby allowing a cancer cell to survive despite an abundance of misfolded and unstable proteins. Inhibition of Hsp90 may have broad therapeutic potential for the treatment of patients with solid tumors and blood-related cancers, including cancers that are resistant to other drugs.
IPI-504 preferentially targets and accumulates in tumor tissues, sparing healthy tissues. In preclinical studies it has demonstrated a broad potential to treat certain cancers as both a single agent as well as in combination with existing anti-cancer drugs. The water-based formulation of IPI-504 is convenient to deliver as an intravenous infusion. Infinity is currently conducting two Phase 1 clinical trials with intravenous formulations of IPI- 504. In July 2005, Infinity initiated the first of these Phase 1 clinical trials in refractory multiple myeloma. In December 2005, Infinity initiated the second Phase 1 clinical trials with IPI-504 in refractory gastrointestinal stromal tumors (GIST). Infinity has also begun developing an oral formulation of IPI-504, which if successful, could be a more convenient route of administration for cancer therapy.
About Siplizumab (MEDI-507)
Siplizumab is a humanized, monoclonal antibody (MAb) that binds to the CD2 receptor found on the surface of T-cells and natural killer (NK) cells. In July 2003, the U.S. Food and Drug Administration (FDA) approved an orphan drug designation for MEDI-507 for the treatment of T-cell lymphoma. In both preclinical and clinical studies, siplizumab has been shown to cause depletion of T-cells. Siplizumab is therefore considered to be an immunomodulator in clinical settings where the depletion of T-cells may have clinical benefits, such as certain autoimmune diseases and T-cell cancers. MedImmune has previously conducted clinical development programs with siplizumab in patients with other conditions, including psoriasis, graft-versus-host disease and renal transplantation. In addition, preclinical studies have also suggested that siplizumab, by binding to the CD2 receptor, may selectively produce cell death and reduce cancerous cells.
About MT103 (MEDI-538)
MT103 is a Bi-Specific T cell Engager (BiTE(R)) molecule being developed by MedImmune and Micromet, Inc. with the intent to treat certain types of B- cell lymphomas. In February 2006, the U.S. Food and Drug Administration (FDA) approved an orphan drug designation for MEDI-538 for the treatment of indolent B-cell lymphoma, excluding chronic lymphocytic leukemia and non-hodgkins lymphoma with central nervous system involvement. BiTE molecules are part of a novel class of antibody derivatives that may have the potential to selectively direct and activate an individual's own immune system to act against cancer cells. This action is believed to occur as a result of the molecule's stimulation of T cells (a very potent type of white blood cell) to target and destroy cancer cells that over-express a specific antigen. MEDI-538 specifically targets the CD19 antigen, which is present on cancerous B cells but not on other types of blood cells or healthy tissues.
About MedImmune, Inc.
MedImmune strives to provide better medicines to patients, new medical options for physicians, rewarding careers to employees, and increased value to shareholders. Dedicated to advancing science and medicine to help people live better lives, the company is focused on the areas of infectious diseases, cancer and inflammatory diseases. With more than 2,500 employees worldwide, MedImmune is headquartered in Maryland. For more information, visit the company's website at http://www.medimmune.com/.
This announcement contains, in addition to historical information, certain "forward-looking statements" regarding the development of product candidates by MedImmune, Inc. Such forward-looking statements are based on current expectations and involve inherent risks and uncertainties, including factors that could delay, divert or change current expectations and could cause actual outcomes and results to differ materially from current expectations. In addition to risks and uncertainties disclosed in MedImmune's filings with the U.S. Securities and Exchange Commission, MedImmune can provide no assurance that these products will be commercially successful. In addition, no assurance exists that development efforts for these products will succeed, that these products will receive required regulatory approval or that, even if regulatory approval is received, they will be commercially successful. MedImmune undertakes no obligation to update any forward-looking statement, whether as a result of new information, future events or otherwise except as may be required by applicable law or regulation.
MedImmune, Inc.
http://www.medimmune.com/
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