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Phase I Study on Suberoylanilide Hydroxyamic Acid (Vorinostat) a Histone Deacetylase Inhibitor, in Palliative Radiotherapy for Advanced Tumors.
Phase I study. Side-effects when combined with standard palliative radiotherapy.
Age
18 - 100 years
Sex
ALL
Healthy Volunteers
No
The Norwegian Radium Hospital
Oslo, Norway
Start Date
February 1, 2007
Primary Completion Date
March 1, 2009
Completion Date
August 1, 2009
Last Updated
May 8, 2023
15
ACTUAL participants
Vorinostat
DRUG
Lead Sponsor
Oslo University Hospital
NCT06719440
NCT07325721
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05926765