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Recent News and Articles on the Keywords: elaprase + hunter + treatment  Related to the article below (Last Update: 12/1/2008)

 News results: Standard Version | Text Version | Image Version Results 1 - 7 of 7 for elaprase hunter treatment. (0.09 seconds) 
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Hudak calls on province to fund ailing boy's treatment
St. Catharines Standard, Canada - Nov 21, 2008
However, he noted there are only six cases of Hunter syndrome in Ontario and Andrew has shown some improvement since his Elaprase treatment began.
Things looking up a bit for Andrew
Welland Tribune,  Canada - Nov 7, 2008
The drug Elaprase, approved by Health Canada in June, can't cure Hunter syndrome, but can improve a person's quality of life. The Lanese family has been ...
A very special evening for Andrew Lanese
Niagarathisweek.com, Canada - Nov 21, 2008
Although there is no cure for Hunter Syndrome, there is a treatment called Elaprase which improves the symptoms of Hunter's. Andrew's father Nick and mother ...
NICK LANESE WONDERS WHY THERE'S NO PROVINCIAL FUNDING FOR SON WHO ...
Welland Tribune,  Canada - Nov 5, 2008
The treatment has been approved by Health Canada. Nick Lanese said the provincial government itself has recently approved Elaprase treatment for two other ...
Shire Settles Claims with Investors of Former Cambridge, MA ...
Xconomy, MA - Nov 12, 2008
TKT developed key drugs in the Shire HGT portfolio including idursulfase (Elaprase), an enzyme-replacement treatment marketed for patients with Hunter ...
Shire HGT Adds 150 Mass. Workers, Genetic Therapy Sales Soar ...
Xconomy, MA - Nov 20, 2008
This means the double-digit sales growth of its treatments, such as idursulfase (Elaprase) for Hunter syndrome, can get lost in the companywide reports. ...BIIB - GENZ
UPDATE: Shire Aims To Grow Sales In Mid-Teens Range By 2015
EasyBourse.com, France - Nov 18, 2008
Shire currently markets Replagal for Fabry's disease and Elaprase for Hunter syndrome, an inherited condition characterized by the gradual deterioration of ...SHPGY
Source: Google News


 

Recent News and Articles on the Keywords: hunter + elaprase + syndrome  Related to the article below (Last Update: 8/7/2008)

Shire Delivers Strong Quarter: Driven by $243m of New Product ...
MarketWatch - Jul 31, 2008
ELAPRASE(R) - Hunter syndrome - During the three months to June 30, 2008 ELAPRASE was approved for commercial sale in Brazil. ELAPRASE is now approved in 40 ...
Dynepo dropped as Shire places its faith in Vyvanse for growth Pharma Times (subscription)
all 39 news articles »  SHPGY
Canada should follow the US example on 'orphan' diseases
Globe and Mail, Canada - Jul 17, 2008
For example, Hunter syndrome (also known as MPS II), an enzyme disorder that affects only about 40 people nationwide, can be treated effectively with a drug ...
Source: Google News

The characterization of a murine model of mucopolysaccharidosis II (Hunter syndrome) -
AR Garcia, J Pan, JC Lamsa, J Muenzer - Journal of Inherited Metabolic Disease, 2007 - Springer
... of mucopolysaccharidosis II (Hunter syndrome) AR Garcia & J. Pan & JC Lamsa & J.
Muenzer ... Mucopolysaccharidosis II (Hunter syndrome): OMIM 309900. ...

[CITATION] FDA OKs 1st Drug for Hunter Syndrome
M Hitti, B Warning

[CITATION] US FDA Clears Shire Drug for Hunter Syndrome
CME Tracker

[CITATION] International Approvals: Nexavar, Elaprase, Aranesp
Y Waknine

[CITATION] International Approvals: Prexige, Elaprase, Micera
Y Waknine

[CITATION] International Approvals: Tysabri, Elaprase, Invega
Y Waknine

International Approvals: Mirena, Champix, Elaprase
Y Waknine - medscape.com
... Idursulfase Intravenous Infusion (Elaprase) for Hunter Syndrome in EU On January
11, the European Commission approved idursulfase intravenous infusion (Elaprase ...

IDURSULFASE IN HUNTER SYNDROME TREATMENT -
G Zareba - Drugs of Today, 2007 - journals.prous.com
... Enzyme replacement therapy with Elaprase (idursulfase, a recently approved
orphan product) is the first treatment for Hunter syndrome. ...
-

[CITATION] FDA Approvals: Xolegel, Keppra, and Elaprase CME/CE
T Month, P Months

Hunter syndrome: to treat or not to treat
J Muenzer, AM Martins - Acta Paediatrica, 2008 - Blackwell Synergy
... Enzyme replacement therapy (ERT) with idursulfase (Elaprase ? ; Shire HGT, Danderyd,
Sweden) for treating patients with Hunter syndrome has recently been ...

Source: Google Scholar
 
 

Elaprase, the first treatment for Hunter syndrome

The FDA ( Food and Drug Administration ) has approved Elaprase ( Idursulfase ), the first product for the treatment of Hunter syndrome ( Mucopolysaccharidosis II, or MPS II ), a rare inherited disease which can lead to premature death.

Hunter syndrome, which usually becomes apparent in children one to three years of age, is a disease in which the person's body is defective in producing the chemical iduronate-2-sulfatase, which is needed to adequately breakdown complex sugars produced in the body.
Symptoms include growth delay, joint stiffness, and coarsening of facial features.
In severe cases, patients experience respiratory and cardiac problems, enlargement of the liver and spleen, neurological deficits, and death.

Elaprase was designated as an orphan product by FDA.
Hunter syndrome is diagnosed in approximately one out of 65,000 to 132,000 births.

Elaprase was approved after a randomized, double-blind, placebo-controlled study of 96 patients with Hunter syndrome showed that the treated participants had an improved capacity to walk.
At the end of the 53–week trial, patients who received Elaprase infusions experienced on average a 38-yard greater increase in the distance walked in six minutes compared to the patients on placebo.

The most serious adverse events reported during the trial were hypersensitivity reactions to Elaprase that could be life-threatening. They included respiratory distress, drop in blood pressure, and seizure. Other frequent, but less serious adverse events included fever, headache and joint pain.

Because of the potential for severe hypersensitivity reactions, appropriate medical support should be readily available when Elaprase is administered.

Source: FDA, 2006

 
 
 
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