Actonel: profile and news






Oscient Pharmaceuticals Reports Financial Results for Fourth ...  07 Mar 2006
During the fourth quarter of 2005, Oscient recorded $8.0 million in revenue from the Company's lead product, FACTIVE(R) (gemifloxacin mesylate) tablets, FDA ... - Genetic Engineering News,

Sunitinib Malate (Sutent) Provides Long-Lasting Responses in ...  Feb 2, 2006
...sunitinib malate (SU11248, Sutent) is effective in patients with gastrointestinal stromal tumors (GIST) who have failed imatinib mesylate therapy, researchers ... - DG News

Novartis loses EMRs for the cancer drug  Feb 21, 2006
Indian Patents Office has terminated the exclusive marketing rights (EMRs) granted to the company on November 10, 2003 for Gleevac (Imatinib Mesylate), a life ... - Sify,

Oscient Pharmaceuticals to Present at Fifth Annual JMP Securities ...  Mar 2, 2006
...and CEO, Steven Rauscher, will provide an overview of the Company including details on the recent sublicense of FACTIVE(R) (gemifloxacin mesylate) tablets in ... - Genetic Engineering News,

Generics Hail Novartis Loss  Feb 10, 2006
...on Gleevec in India late last month, more than half a dozen Indian drug companies are ready to launch the generic version of Imatinib Mesylate, a lifesaving ... - Red Herring,

New Hope for Stomach Cancer  Mar 1, 2006
For a few years, the drug Gleevec (imatinib mesylate, STI571, STI-571, or STI 571) kept Russo's cancer in check. But like many patients, he became resistant. ... - ABC30.com,

Subcutaneous Amifostine Feasible During Radiotherapy for Head and ...  Mar 1, 2006
...in the Archives of Otolaryngology Head and Neck Surgery for February, the patients received a 200-mg dose of the oral anti-emetic dolasetron mesylate 1 to 2 ... - Cancerpage.com,

Novartis denied patent for cancer drug  Feb 9, 2006
Assistant Controller of Patents & Designs V Rengasamy rejected the application on January 25 on the ground that the drug, Imatinib Mesylate, did not qualify ... - Rediff,

MDCT Appearance of Gastrointestinal Stromal Tumors After Therapy ...  Feb 14, 2006
OBJECTIVE. Our objective was to determine the MDCT appearance of gastrointestinal stromal tumors (GISTs) after treatment with imatinib mesylate. CONCLUSION. ... - Am J Roentgenology (subscription)

Cell Genesys Reports Fourth Quarter and Full Year 2005 Results  Feb 21, 2006
Nineteen CML patients with molecular evidence of persistent leukemia despite more than one year of Gleevec(R) (imatinib mesylate) therapy were treated with ... - International News Service,

Antigenics Reports Fourth Quarter and Year-End 2005 Financial ...  Feb 23, 2006
Phase 2 clinical study is underway with AG-858, a patient-specific therapeutic cancer vaccine, in combination with Gleevec(R) (imatinib mesylate, Novartis) for ... - Genetic Engineering News,

New Hope For Stomach Cancer  Feb 24, 2006
Gleevec, or imatinib mesylate, blocks the tumor cells' ability to grow and divide. However, Gleevec is not a long-term solution for cancers. ... - WFtv.com,

NOVARTIS PATENT APPLICATION FOR CANCER DRUG FOUND INSUFFICIENT IN ...  Feb 16, 2006
Indian authorities have rejected Swiss pharmaceutical giant Novartis' patent application for the cancer drug imatinib mesylate, generally known by the brand ... - Weekly Trade News Digest,

Test Now Available to Detect Resistance to Gleevec® in Chronic ...  Feb 23, 2006
...a test available to the public that can detect whether a patient with chronic myeloid leukemia (CML) is resistant to treatment with Gleevec® (imatinib mesylate ... - Cancer Consultants (press release),

New drug fights GI tumors  Feb 22, 2006
...gastrointestinal stromal tumors (GIST). Gleevec, manufactured by Novartis, is the brand name for imatinib mesylate. Sutent (sunitinib) delays ... - myDNA.com,

Webcast Alert: Oscient Pharmaceuticals Announces Date for Release ...  Feb 22, 2006
The Company is marketing FACTIVE(R) (gemifloxacin mesylate) tablets, approved by the FDA for the five-day treatment of acute bacterial exacerbations of chronic ... - Business Wire (press release),

Senetek Licenses Invicorp(R) Erectile Dysfunction Treatment to ...  Feb 21, 2006
Invicorp® is Senetek's patented injectable combination of phentolamine mesylate and vasoactive intestinal polypeptide for the treatment of ED. ... - Yahoo! News (press release)

Oscient Pharmaceuticals and Pfizer Enter Agreement for FACTIVE ...  Feb 7, 2006
Oscient Pharmaceuticals Corporation (Nasdaq: OSCI) has sublicensed the commercialization rights to FACTIVE(R) (gemifloxacin mesylate) tablets in Mexico to ... - Genetic Engineering News,

Senetek Licenses Invicorp(R) Erectile Dysfunction Treatment to ...  Feb 21, 2006
Invicorp(R) and the erectile dysfunction market Invicorp(R) is Senetek's patented injectable combination of phentolamine mesylate and vasoactive intestinal ... - PR Newswire (press release),

Oscient Pharmaceuticals and Pfizer Enter Agreement for FACTIVE ...  Feb 7, 2006
7, 2006 - Oscient Pharmaceuticals Corporation (Nasdaq: OSCI) has sublicensed the commercialization rights to FACTIVE(R) (gemifloxacin mesylate) tablets in ... - PharmaLive.com (press release),

Senetek Licenses Invicorp Erectile Dysfunction Treatment to ...  Feb 21, 2006
Invicorp(R) is Senetek's patented injectable combination of phentolamine mesylate and vasoactive intestinal polypeptide for the treatment of ED. ... - PharmaLive.com (press release),

Oscient Pharmaceuticals y Pfizer celebran acuerdo por las...  Feb 7, 2006
The Company is marketing FACTIVE(R) (gemifloxacin mesylate) tablets, approved by the FDA for the treatment of acute bacterial exacerbations of chronic ... - Nosis NyM,

UPDATE 1-Roche to discontinue US sales of AIDS drug  Feb 6, 2006
Roche said its Invirase (saquinavir mesylate) HIV drug in 500 milligram tablet form is the preferred medicine as part of a combination treatment to prevent ... - Reuters

Patent remedy for India’s health  Feb 9, 2006
Controversy raged last year after Novartis was granted an exclusive marketing right for the anti-cancer drug imatinib mesylate, commonly known as Gleevec. ... - Indian Express,

Novartis denied patent for cancer drug, Gleevec  Feb 9, 2006
The application was rejected on January 25 on the ground that the drug, Imatinib Mesylate, did not qualify for patenting in India as the novelty of the drug ... - Myiris.com,

Roche to Focus Resources on Availability of Invirase, Now ...  Feb 6, 2006
Invirase® (saquinavir mesylate) capsules and Fortovase® (saquinavir) soft gelatin capsules are not bioequivalent and cannot be used interchangeably. ... - DG News

Genzyme Launches Key Test to Monitor Gleevec(R) Resistance  Feb 9, 2006
...availability of an important new test to monitor drug resistance in chronic myeloid leukemia (CML) patients who are treated with Gleevec(R) (imatinib mesylate ... - International News Service,

Pfizer acquires rights to Oscient antibiotic in Mexico  Feb 9, 2006
Factive (gemifloxacin mesylate) is currently approved in the US for the treatment of community-acquired pneumonia (CAP) of mild to moderate severity and acute ... - Pharmaceutical Business Review

Power3's Invited Review on Biomarkers and Test for ALS ...  Feb 14, 2006
...for Differential Diagnosis of Parkinson's Disease" and "Biomarkers for Diagnosis and Targeting of Resistance and Sensitivity to Imatinib Mesylate in Chronic ... - Genetic Engineering News,

New oral drug could make Thalassemia treatment less painful for ...  Feb 8, 2006
...children with Thalassemia major needed regular treatment to remove the excess iron from their bodies for which Desferal (R) (deferoxamine mesylate) (Desferal (R ... - Daily Times,

Genzyme launches test to monitor Gleevec resistance  Feb 13, 2006
...the availability of an important new test to monitor drug resistance in chronic myeloid leukemia (CML) patients who are treated with Gleevec (imatinib mesylate ... - News-Medical.net,

Pharmaceutical Companies Look to Biomarkers to Help in Increasing ...  Feb 2, 2006
Several companion diagnostics for molecularly targeted oncology drugs, including trastuzumab (Genentech's Herceptin), imatinib mesylate (Novartis's Gleevec ... - PharmaLive.com (press release),


Other information


Indication
For the treatment of Paget's disease of the bone (osteitis deformans); Postmenopausal and glucocorticoid-induced osteoporosis

Pharmacology
Risedronate is a pyridinyl bisphosphonate that inhibits osteoclast-mediated bone resorption and modulates bone metabolism and is indicated for the treatment and prevention of osteoporosis in postmenopausal women.

Mechanism Of Action
The action of Risedronate on bone tissue is based partly on its affinity for hydroxyapatite, which is part of the mineral matrix of bone. Risedronate also targets farnesyl pyrophosphate (FPP) synthase. Nitrogen-containing bisphosphonates (such as pamidronate, alendronate, risedronate, ibandronate and zoledronate) appear to act as analogues of isoprenoid diphosphate lipids, thereby inhibiting FPP synthase, an enzyme in the mevalonate pathway. Inhibition of this enzyme in osteoclasts prevents the biosynthesis of isoprenoid lipids (FPP and GGPP) that are essential for the post-translational farnesylation and geranylgeranylation of small GTPase signalling proteins. This activity inhibits osteoclast activity and reduces bone resorption and turnover. In postmenopausal women, it reduces the elevated rate of bone turnover, leading to, on average, a net gain in bone mass.

Drug Category
Antiresorptives; Bisphosphonates; Antihypocalcemic Agents;

Brand Names/Synonyms
Actonel; Pyridine N-Oxide; Pyridostigmine Bromide; Pyridostigmine Bromine; Risedronate; Risedronate Sodium; Risedronic Acid

Dosage Forms
TABLET

Absorption
Rapid absorption (~1 hr) after an oral dose, occurs throughout the upper gastrointestinal tract

Interactions
-->Interactions for Risedronate:

No specific drug-drug interaction studies were performed. Risedronate is not metabolized and does not induce or inhibit hepatic microsomal drug-metabolizing enzymes (Cytochrome P450).

Calcium Supplements/Antacids

Co-administration of ACTONEL and calcium, antacids, or oral medications containing divalent cations will interfere with the absorption of ACTONEL.

Hormone Replacement Therapy

One study of about 500 early postmenopausal women has been conducted to date in which treatment with ACTONEL (5 mg/day) plus estrogen replacement therapy was compared to estrogen replacement therapy alone. Exposure to study drugs was approximately 12 to 18 months and the primary endpoint was change in BMD. If considered appropriate, ACTONEL may be used concomitantly with hormone replacement therapy.

Aspirin/Nonsteroidal Anti-Inflammatory Drugs (NSAIDs)

Of over 5700 patients enrolled in the ACTONEL Phase 3 osteoporosis studies, aspirin use was reported by 31% of patients, 24% of whom were regular users (3 or more days per week). Forty-eight percent of patients reported NSAID use, 21% of whom were regular users. Among regular aspirin or NSAID users, the incidence of upper gastrointestinal adverse experiences in ACTONEL-treated patients (24.5%) was similar to that in placebo-treated patients (24.8%).

H2 Blockers and Proton Pump Inhibitors (PPIs)

Of over 5700 patients enrolled in the ACTONEL Phase 3 osteoporosis studies, 21% used H2 blockers and/or PPIs. Among these patients, the incidence of upper gastrointestinal adverse experiences in the ACTONEL-treated patients was similar to that in placebo-treated patients.

Drug/Laboratory Test Interactions

Bisphosphonates are known to interfere with the use of bone-imaging agents. Specific studies with ACTONEL have not been performed.



Chemical IUPAC Name
(1-hydroxy-1-phosphono-2-pyridin-3-yl-ethyl)phosphonicacid

Chemical Formula
C7H11NO7P2

Half Life
1.5 hours

Drug Type
Approved Drug

# Accession No
APRD00410

CAS Registry Number
105462-24-6

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