Brightline-2: A Study to Test Whether Brigimadlin (BI 907828) Helps People With Cancer in the Biliary Tract, Pancreas, Lung or Bladder
NCT05512377
Biliary Tract Cancer, Biliary Tract Diseases
Mobile, Alabama, United States
View Trial DetailsNCT Number: NCT04896931
Permanent, prospective, multicenter registry including all kind of oncological therapy lines and procedures, clinical outcome, translational research (biobanking) and QoL for all types of biliary tract cancers.
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Notify Me18 year and older
All sexes
Observational
Universitätsklinikum Freiburg, Freiburg im Breisgau, Baden-Wurttemberg, Germany
Permanent, prospective, multicenter registry including all kind of oncological therapy lines and procedures, clinical outcome, translational research (biobanking) and QoL for all types of biliary tract cancers. The registry does not define any medical intervention and does not evaluate the efficacy or safety of the treatment decision made by the investigator. Every adverse event whether related to a treatment or not, will neither be documented in the trial´s eCRF nor be reported to the leading investigators of this study.
Objectives: • To establish a registry with a representative BTC-patient population in German-speaking Europe (mainly DACH region) for current and future research. The study registry is not based on a primary endpoint. The data collection includes (among basic patient-/tumor-/treatment- characteristics) the survey of quality of life (EORTC-C30), a so-called patient-reported outcome (PRO) and - if available - the collection of tissue samples for translational accompanying projects.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Through study completion, an average of 2 years
To establish a representative BTC-patient population in German-speaking Europe in an agile platform study design for future research
Time frame: Through study completion, an average of 2 years
Correlate medical history with patient outcome, find prevalent medical history associated with BTC chancer
Time frame: Through study completion, an average of 2 years
EORTC-QLQC30 according to EORTC scoring manual
Time frame: Through study completion, an average of 2 years
progression-free survival in different BTC subgroups and therapy lines. As for the main objective, there is no formal secondary endpoint in a registry study. Therfore, in this section we will explain the main data to be collected and the main outcome measures.
Time frame: Through study completion, an average of 2 years
disease-free survival in different BTC subgroups and therapy lines. As for the main objective, there is no formal secondary endpoint in a registry study. Therfore, in this section we will explain the main data to be collected and the main outcome measures.
Time frame: Through study completion, an average of 2 years
overall survival in different BTC subgroups and therapy lines. As for the main objective, there is no formal secondary endpoint in a registry study. Therfore, in this section we will explain the main data to be collected and the main outcome measures.
Time frame: Through study completion, an average of 2 years
mortality for perioperative and palliative therapy procedures
Time frame: Through study completion, an average of 2 years
morbidity for perioperative and palliative therapy procedures
Time frame: Through study completion, an average of 2 years
establish a sample collection for future molecular/genetic biomarker characterization
Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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