ORLANDO, Fla., Dec. 9 /PRNewswire-FirstCall/ -- 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.)
* "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.
SOURCE MedImmune, Inc.
CONTACT: Media: Kate Barrett, +1-301-398-4320, or Investors: Peter
Vozzo, +1-301-398-4358, both of MedImmune, Inc.