Navigation Links
Norditropin(R) Approved for Treatment of Children with Short Stature Associated with Turner Syndrome
Date:9/21/2007

Treatment with Norditropin increases gain in height for girls with Turner

syndrome

PRINCETON, N.J., Sept. 21 /PRNewswire-FirstCall/ -- Novo Nordisk today announced that Norditropin(R) (somatropin [rDNA origin] injection) received approval from the U.S. Food and Drug Administration (FDA) for the treatment of children with short stature associated with Turner syndrome. Turner syndrome is a rare chromosomal condition caused by complete or partial absence of the second sex chromosome (X chromosome) in females. This occurs in approximately 1 in 2,500 live female births, and in as many as 10 percent of all miscarriages worldwide. Short stature is the most common feature associated with Turner syndrome affecting the majority of patients (90 - 100 percent depending on the chromosomal abnormalities).

"Treatment of short stature in girls with Turner syndrome is the second new indication granted this summer for Norditropin, which recently received an approval to treat children with short stature associated with Noonan syndrome," said Martin Soeters, president of Novo Nordisk Inc. "Novo Nordisk is committed to our biopharmaceutical business unit, and we will continue to conduct research in rare disorders where there are currently treatment gaps."

This FDA approval signifies advancement in dosing capabilities, giving physicians the option of dosing at higher than existing treatment options. Results from a pivotal clinical trial illustrated that treatment with Norditropin at the higher dosing level of .067 mg/kg/day resulted in 80 percent of Turner syndrome patients reaching a normal adult height compared to only 53 percent at a lower dosing level.

"I know first hand from my practice that short stature can be a social and self image concern for girls with Turner syndrome," said Judith Ross, M.D., Professor, Department of Pediatrics at Thomas Jefferson University, Philadelphia. "Clinical data for Norditropin in girls
'/>"/>

SOURCE Novo Nordisk
Copyright©2007 PR Newswire.
All rights reserved

Page: 1 2 3 4 5 6

Related medicine technology :

1. Major Manufacturer of Unapproved and Adulterated Drugs
2. Survey: Migraine Patients Taking Potentially Addictive Barbiturate or Opioid Medications Not Approved by FDA as Migraine Treatments
3. Point of Care Strep Tests Speed Treatment, Lower Costs
4. Rapid HIV Testing Increases Possibility of Treatment
5. Data Available From Erbitux Phase III Study in First-Line Treatment of Advanced Lung Cancer
6. Pixantrone Combination Therapy for First-line Treatment of Aggressive Non-Hodgkins Lymphoma Results in Reduction in Severe Toxicities Including Heart Damage When Compared to Doxorubicin-based Therapy
7. AVI BioPharma Partner Cook Medical Announces Completion of Patient Enrollment for APPRAISAL Phase II Clinical Trial for Treatment of Cardiovascular Disease
8. BusinessWeek Article Highlights Promising Breakthrough Treatment for Advanced Coronary Artery Disease
9. TransPharma Medical Announces Positive Results of Phase I Clinical Trials for Transdermal Delivery of hPTH (1-34) for Osteoporosis Treatment
10. TMC125 Showed Significant Virologic Response at Week 24 in Treatment-Experienced HIV Patients With NNRTI Resistance in Phase 3 Trials
11. New Phase 3 Study Published in The Lancet Evaluates Efficacy and Safety of Prezista/Ritonavir vs. Kaletra as Part of HIV Combination Therapy in Treatment-Experienced Adults With HIV
Post Your Comments:
*Name:
*Comment:
*Email:
Breaking Medicine Technology:RetireSafe Announces Intention to Key Vote Senator Dorgan's Drug Importation Amendment (SA 2793) 2Dynatronics Receives 180-Day NASDAQ Extension 2Berger & Montague, P.C., Files Class Action Against Hemispherx Biopharma, Inc. Extending the End of the Class Period to December 1, 2009, When the Company Announced That the FDA Found No Evidence of Efficacy of Its Drug 2Berger & Montague, P.C., Files Class Action Against Hemispherx Biopharma, Inc. Extending the End of the Class Period to December 1, 2009, When the Company Announced That the FDA Found No Evidence of Efficacy of Its Drug 3Congressional Health Reform Bill Falls Short on Comprehensive and Affordable Coverage for Low Income Children 61194 1Congressional Health Reform Bill Falls Short on Comprehensive and Affordable Coverage for Low Income Children 61194 2Congressional Health Reform Bill Falls Short on Comprehensive and Affordable Coverage for Low Income Children 61194 3Dendreon Reports Third Quarter 2009 Financial Results and Continuing Progress Toward PROVENGE Commercialization 14801 1Dendreon Reports Third Quarter 2009 Financial Results and Continuing Progress Toward PROVENGE Commercialization 14801 2Dendreon Reports Third Quarter 2009 Financial Results and Continuing Progress Toward PROVENGE Commercialization 14801 3Dendreon Reports Third Quarter 2009 Financial Results and Continuing Progress Toward PROVENGE Commercialization 14801 4Dendreon Reports Third Quarter 2009 Financial Results and Continuing Progress Toward PROVENGE Commercialization 14801 5Dendreon Reports Third Quarter 2009 Financial Results and Continuing Progress Toward PROVENGE Commercialization 14801 6Dynatronics to Release First Quarter Results Friday November 13 2009 3B Conference Call Set for 1 3A30 p m ET 6188 1