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Gloucester Pharmaceuticals Reports Positive Interim Phase II Data on Romidepsin for Peripheral T-Cell Lymphoma at the 2006 American Society of Hematology (ASH) Annual Meeting.


Durable Complete Responses Observed in Various Subtypes of Peripheral T-Cell Lymphoma (PTCL PTCL Pakistan Telecommunication Company Limited
PTCL Peripheral T Cell Lymphoma
PTCL Physical and Theoretical Chemistry Laboratory
PTCL Pakistan Tobacco Company Limited
) with Single-Agent Romidepsin

Company Expects to Initiate a Pivotal Study in PTCL in Early 2007

CAMBRIDGE, Mass. -- Gloucester Pharmaceuticals, Inc., a privately held cancer therapeutics development company, today announced interim data for romidepsin (formerly known as depsipeptide, FK228) as a treatment for peripheral T-cell lymphoma (PTCL) at the American Society of Hematology Annual Meeting held in Orlando, FL. The data presented are part of an interim analysis of a phase II study sponsored by the National Cancer Institute (NCI See Liberate. ) under a Cooperative Research and Development Agreement “CRADA” redirects here. For other uses, see CRADA (disambiguation).

A Cooperative Research and Development Agreement (CRADA) is an agreement between a government agency and a private company to work together.
 (CRADA CRADA Cooperative Research And Development Agreement ) with Gloucester.

Dr. Richard L. Piekarz of the National Cancer Institute and a principal investigator in the NCI's ongoing clinical trial of romidepsin presented Abstract #2469 "Phase II Trial of Romidepsin, FK228, in Cutaneous cutaneous /cu·ta·ne·ous/ (ku-ta´ne-us) pertaining to the skin.

cu·ta·ne·ous
adj.
Of, relating to, or affecting the skin.


Cutaneous
Pertaining to the skin.
 and Peripheral T-Cell Lymphoma: Clinical Activity and Medical Markers" in a general poster session on Sunday, December 10th.

The interim results reported on 36 patients with PTCL. An overall response rate of 30% (11/36) was reported, with 3 complete responses (8%) and 8 partial responses (22%). The median duration of response in PTCL was reported as 12+ months. Overall, the most common adverse events reported were fatigue, nausea, and vomiting. In a separate release issued today Gloucester announced the interim results from this trial for 42 patients with cutaneous T-cell lymphoma Cutaneous T-Cell Lymphoma Definition

Cutaneous T-cell lymphoma (CTCL) is a malignancy of the T-helper (CD4+) cells of the immune system.
Description
 (CTCL CTCL Cutaneous T Cell Lymphoma ).

Commenting on the Piekarz poster presentation, Jean Nichols, Ph.D., Executive Vice President and Chief Scientific Officer at Gloucester said, "We are quite encouraged with the results reported for peripheral T-cell lymphoma. Significant clinical responses have now been observed in peripheral T-cell and cutaneous T-cell lymphoma patients, suggesting that romidepsin has activity in multiple T-cell lymphomas." Dr. Nichols further commented, "Based on this encouraging data, we expect to initiate a Gloucester-sponsored international pivotal study in PTCL in the first quarter of 2007."

About PTCL

Peripheral T-cell lymphoma accounts for about 10-15% of all cases of non-Hodgkin's lymphoma. It can occur at any age from young adulthood to old age and is slightly more common in men than in women. PTCL is a particularly aggressive form of lymphoma with a short median duration of life expectancy (approximately two years) from diagnosis.

About Romidepsin (Depsipeptide)

In July 2006 the International Nonproprietary Names (INN) body of the World Health Organization (WHO) and the United States Adopted Names United States Adopted Names See USAN.  (USAN USAN United States Adopted Name.

USAN
abbr.
United States Adopted Names (used for nonproprietary names of drugs adopted by a committee of medical professionals and drug manufacturers)



USAN
) Council approved the nonproprietary (generic) name romidepsin for depsipeptide (FK228). Romidepsin is a novel agent in a new class of anti-cancer drugs known as histone deacetylase inhibitors. The Company is conducting a pivotal study of romidepsin for patients with cutaneous T-cell lymphoma (CTCL). Romidepsin has received both Fast Track and Orphan Drug Designation by the Food and Drug Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
), and Orphan Drug Designation from the European Agency for the Evaluation of Medicinal Products (EMEA (Europe, Middle East, Africa) Refers to that region of the world. For example, one might see products packaged differently for the UK, EMEA and Asia Pacific markets. ). Romidepsin is also in clinical trials for a variety of other hematologic malignancies and solid tumors including peripheral T-cell lymphoma, hormone refractory prostate cancer and multiple myeloma. These trials and others are being conducted by the Company or the National Cancer institute (NCI), under a Cooperative Research and Development Agreement (CRADA) with the Company.

About Gloucester Pharmaceuticals, Inc.

Gloucester Pharmaceuticals, Inc. is a privately held, venture-backed company that develops and commercializes innovative products for the treatment of cancer patients. Gloucester is headquartered in Cambridge, MA. For more information on Gloucester and our clinical development program visit our website at www.gloucesterpharma.com or call 888-GPI-CTCL (888-474-2825).
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Copyright 2006, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Date:Dec 12, 2006
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