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Multicenter Non-interventional Study to Investigate Safety, Tolerability and Efficacy of Nab-paclitaxel in Clinical Routine Treatment of First-line Pancreatic Cancer Patients
This observational program collects data on tolerability, safety and efficacy regarding the use of Abraxane in metastatic pancreatic cancer patients in the daily clinical routine. Additionally data on dosage that is actually used in these patients will be collected. Patients who have pancreatic cancer and additional diseases can be documented in this study, too. Collected data might generate learnings on the optimal use of Abraxane in the daily routine setting.
This observational program is aimed at gaining tolerability, safety and efficacy data with the routine use of Abraxane in its labeled indication in metastatic pancreatic cancer. Additionally data on real life dosing in daily clinical routine will be analyzed. A detailed record of the medical history including co-morbidities and pre-treatment regimens will allow analysis of the impact thereof on tolerability, dosage and efficacy. Hands-on experience with nab-paclitaxel is very limited in Austria and an non-interventional study could enhance knowledge on optimal drug handling and Adverse Event management.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
BHB Eisenstadt
Eisenstadt, Austria
LKH Feldkirch
Feldkirch, Austria
Medical University Graz
Graz, Austria
Medical University Innsbruck
Innsbruck, Austria
KH Elisabethinen Klagenfurt
Klagenfurt, Austria
LKH Klagenfurt
Klagenfurt, Austria
KH Krems
Krems, Austria
LKH Leoben
Leoben, Austria
KH Barmherzige Schwestern Linz
Linz, Austria
LKH Salzburg
Salzburg, Austria
Start Date
May 8, 2015
Primary Completion Date
September 7, 2020
Completion Date
September 7, 2020
Last Updated
October 19, 2020
317
ACTUAL participants
Abraxane
DRUG
Gemcitabine
DRUG
Lead Sponsor
Celgene
NCT07409272
NCT05065801
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 ConditionsNCT04605913