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DR ANTHONY MELVIN CRASTO, WORLDDRUGTRACKER

Generic Licensing News, Featured product, Bosentan

 Uncategorized  Comments Off on Generic Licensing News, Featured product, Bosentan
Jun 122013
 

Generic Licensing News

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Click here to contact Zack Systems SpA about this product.

 

BOSENTAN

Bosentan is a dual endothelin receptor antagonist important in the treatment of pulmonary artery hypertension (PAH).

Bosentan belongs to a class of drugs known as endothelin receptor antagonists (ERAs). Patients with PAH have elevated levels of endothelin, a potent blood vessel constrictor, in their plasma and lung tissue. Bosentan blocks the binding of endothelin to its receptors, thereby negating endothelin’s deleterious effects.

bosentan

Bosentan is a dual endothelin receptor antagonist used in the treatment of pulmonary artery hypertension (PAH). It is licensed in the United States, the European Union and other countries by Actelion Pharmaceuticals for the management of PAH under the trade name Tracleer.

Bosentan is indicated mainly for the treatment of pulmonary hypertension. In 2007, bosentan was approved in the European Union also for reducing the number of new digital ulcers in patients with systemic sclerosis and ongoing digital ulcer disease.Bosentan is a competitive antagonist of endothelin-1 at the endothelin-A (ET-A) and endothelin-B (ET-B) receptors. Under normal conditions, endothelin-1 binding of ET-A or ET-B receptors causes pulmonary vasoconstriction. By blocking this interaction, bosentan decreases pulmonary vascular resistance. Bosentan has a slightly higher affinity for ET-A than ET-B.

In the United States, bosentan is indicated for the treatment of pulmonary arterial hypertension (WHO Group I) in patients with WHO Class II-IV symptoms, to improve exercise capacity and decrease the rate of clinical worsening.[1]

Warnings

Due to potential hepatotoxicity, the FDA requires monthly monitoring of liver function tests while taking Bosentan.

Bosentan use requires hematocrit monitoring due to potential onset of anemia. [2]

Hormone-based contraception is not possible in women taking Bosentan, due to a pharmacokinetic interaction. [3]

Bosentan is absolutely contraindicated in pregnancy because of its teratogenicity. Category X.

  1. http://www.tracleer.com/pdf/09%20276%2001%2000%200809_Tra%20PI_4%20Pg_081409pdf.pdf
  2. http://www.ionchannels.org/showabstract.php?pmid=15875338
  3. http://www.ionchannels.org/showabstract.php?pmid=15875338

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ViroPharma Receives Orphan Drug Designation For Maribavir In Europe

 drugs, Phase 3 drug  Comments Off on ViroPharma Receives Orphan Drug Designation For Maribavir In Europe
Jun 122013
 

Maribavir

ViroPharma Receives Orphan Drug Designation For Maribavir In Europe
The Herald | HeraldOnline.com
We commend the European Commission for providing incentives such as this for the development of drugs for rare and life threatening diseases.” ViroPharma is currently conducting two Phase 2 dose ranging studies of oral maribavir at one of three doses

read all at

http://www.heraldonline.com/2013/06/11/4934867/viropharma-receives-orphan-drug.html

Maribavir (originally named 1263W94) is an experimental oral antiviral drug candidate licensed by ViroPharma from GlaxoSmithKline in 2003 for the prevention and treatment of human cytomegalovirus (HCMV) disease in hematopoietic stem cell/bone marrow transplant patients. The mechanism by which maribavir inhibits HCMV replication is by inhibition of an HCMV encoded protein kinase enzyme called UL97 or pUL97. Maribavir showed promise in Phase II clinical trials and was granted fast track status, but failed to meet study goals in a Phase III trial. However, the dosage used in the Phase III trial may have been too low to be efficacious.

A Phase II study with maribavir demonstrated that prophylaxis with maribavir displayed strong antiviral activity, as measured by statistically significant reduction in the rate of reactivation of CMV in recipients of hematopoietic stem cell/bone marrow transplants. In an intent-to-treat analysis of the first 100 days after the transplant, the number of subjects who required pre-emptive anti-CMV therapy was statistically significantly reduced with maribavir compared to placebo.

ViroPharma conducted a Phase III clinical study to evaluate the prophylactic use for the prevention of cytomegalovirus disease in recipients of allogeneic stem cell transplant patients. In February 2009, ViroPharma announced that the Phase III study failed to achieve its goal, showing no significant difference between maribavir and a placebo at reducing the rate at which CMV DNA levels were detected in patients.

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Promising Results in Clinical Study for Acne Drug Candidate

 drugs  Comments Off on Promising Results in Clinical Study for Acne Drug Candidate
Jun 122013
 

Acne drug

 

Promising Results in Clinical Study for Acne Drug Candidate
SkinInc.com
Novan Therapeutics,announced results from a recent clinical trial demonstrating that nitric oxide releasing drug candidate SB204 reduces colonization of the acne causing bacteria Propionibacterium acnes (P. acnes) in the skin of healthy volunteers. This study in combination with Novan’s earlier findings regarding sebum production, suggests the formulation may be capable of targeting multiple factors in acne.

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read all at

http://www.skininc.com/skinscience/ingredients/Promising-Results-in-Clinical-Study-for-Acne-Drug-Candidate-211007471.html

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Ariad begins Phase 2 trial of Iclusig to treat GI tumors

 drugs  Comments Off on Ariad begins Phase 2 trial of Iclusig to treat GI tumors
Jun 122013
 

 

Ponatinib

Ariad begins Phase 2 trial of Iclusig to treat GI tumors


Boston Business Journal (blog)

Ariad Pharmaceuticals, Inc.  has launched a Phase 2 trial to test its approved leukemia drug Iclusig as a potential treatment for gastrointestinal stromal tumors (GIST).

The Cambridge, Mass-based company’s drug was approved by the U.S. Food and Drug Administration in December 2012. It’s approved to treat certain patients chronic myeloid leukemia (CML) that is resistant or intolerant to other drugs and Philadelphia chromosome positive acute lymphoblastic leukemia (Ph+ ALL).

read all at

http://www.bizjournals.com/boston/blog/bioflash/2013/06/ariad-trial-cancer-drug.html

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