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Neotrofin for Treatment of Chemotherapy-Induced Peripheral Neuropathy
This study has been completed.
Study NCT00041795   Information provided by NeoTherapeutics
First Received: July 16, 2002   Last Updated: June 23, 2005   History of Changes

July 16, 2002
June 23, 2005
January 2002
 
 
 
Complete list of historical versions of study NCT00041795 on ClinicalTrials.gov Archive Site
 
 
 
Neotrofin for Treatment of Chemotherapy-Induced Peripheral Neuropathy
A Multi-Center, Double-Blind, Randomized, Placebo-Controlled Study of Neotrofin to Treat Patients With Sensory or Motor Neuropathy Caused by Chemotherapy for Cancer

This study will assess the safety and efficacy of Neotrofin in treating the peripheral neuropathy that results from chemotherapy for cancer.

 
Phase II
Interventional
Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
  • Peripheral Nervous System Diseases
  • Chemotherapy-Induced Peripheral Neuropathy
Drug: leteprinim potassium (Neotrofin)
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
50
 
 
  • Patient must have diagnosis of cancer and be receiving or have received chemotherapy that has resulted in sensory or motor neuropathy.
  • Sensory or motor neuropathy must be >/= grade 2 per Common Toxicity Criteria at baseline.
  • In patients diagnosed with multiple myeloma, grade 1 sensory or motor neuropathy is acceptable.
  • Patient must have normal hematological cell counts.
  • Patient must have a life expectancy of >/= 3 months.
Both
18 Years to 80 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00041795
 
082-2001-005
NeoTherapeutics
 
 
NeoTherapeutics
July 2002

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP