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Genta Receives Key Patent Related to Oral Gallium Compound G4544

Tuesday, April 15, 2008 General News
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BERKELEY HEIGHTS, N.J., April 14 Genta Incorporated(Nasdaq: GNTA) today announced that the Company has received notice that itspatent application covering novel pharmaceutical gallium compositions andcomplexes has been allowed by the U.S. Patent Office. Issued U.S. Patent7,354,952 extends the intellectual property surrounding the Company'sfranchise of oral gallium-containing products that are intended as potentialtreatment for diseases associated with accelerated bone loss. The leadcompound in this investigational pipeline, G4544, was developed incollaboration with Emisphere Technologies, Inc. (Nasdaq: EMIS) and hascompleted its initial Phase 1 dose-ranging study. Results of this study willbe presented at the Annual Meeting of the American Society of ClinicalOncology (ASCO) that takes place in Chicago, IL from May 30-June 3, 2008.
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With continued progress in the oral formulation program, the Company haselected to seek a buyer for the intravenous formulation of its on-marketproduct from this franchise, Ganite(R) (gallium nitrate injection). Theactive ingredient in both Ganite and G4544 is ionic gallium, which isreversibly incorporated into bone where its acts as a potent inhibitor of boneresorption and possibly as a mild anabolic agent to enhance bone formation.Ganite is approved by the U.S. Food and Drug Administration for treatment ofpatients with cancer-related hypercalcemia that is resistant to hydration.Ganite is exclusively marketed in the U.S. by Genta and is available topatients outside the U.S. on a "named-patient" basis.
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About Genta

Genta Incorporated is a biopharmaceutical company with a diversifiedproduct portfolio that is focused on delivering innovative products for thetreatment of patients with cancer. Two major programs anchor the Company'sresearch platform: DNA/RNA-based Medicines and Small Molecules. Genasense(R)(oblimersen sodium) Injection is the Company's lead compound from its DNA/RNAMedicines program. Genta is currently recruiting patients to the AGENDATrial, a global Phase 3 trial of Genasense in patients with advanced melanoma.The leading drug in Genta's Small Molecule program is Ganite(R) (galliumnitrate injection), which the Company is exclusively marketing in the U.S. fortreatment of symptomatic patients with cancer related hypercalcemia that isresistant to hydration. The Company has developed G4544, an oral formulationof the active ingredient in Ganite, that has recently entered clinical trialsas a potential treatment for diseases associated with accelerated bone loss.The Company is also developing tesetaxel, a novel, orally absorbed, semi-synthetic taxane that is in the same class of drugs as paclitaxel anddocetaxel. Ganite and Genasense are available on a "named-patient" basis incountries outside the United States. For more information about Genta, pleasevisit our website at: www.genta.com.

Safe Harbor

This press release may contain forward-looking statements with respect tobusiness conducted by Genta Incorporated. By their nature, forward-lookingstatements and forecasts involve risks and uncertainties because they relateto events and depend on circumstances that will occur in the future. Forward-looking statements include, without limitation, statements about:

The Company does not undertake to update any forward-looking statements.There are a number of factors that could cause actual results and developmentsto differ materially. For a discussion of those risks and uncertainties,please see the Company's Annual Report on Form 10-K for 2007 and its mostrecent quarterly report on Form 10-Q.-- the Company's ability to obtain necessary regulatory approval for Genasense(R) from the U.S. Food and Drug Administration ("FDA") or European Medicines Agency ("EMEA"); -- the safety and efficacy of the Company's products or product candidates; -- the Company's assess
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