The primary objective of the trial is to determine the efficacy of VANDETANIB monotherapy or VANDETANIB plus GEMCITABINE or PLACEBO plus GEMCITABINE in prolonging the progression-free survival (PFS) at the trial closure in patients with advanced (unresectable or metastatic) biliary tract cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
174
300 mg as a once daily oral dose, from Day 1 until disease progression or unacceptable toxicity or consent withdrawal whichever occurs first
100 mg as a once daily oral dose, from Day 1 until disease progression or unacceptable toxicity or consent withdrawal whichever occurs first
administered intravenously at 1000 mg/m2 over 30 minutes on Days 1 and 8 of each 21-day cycle up to 6 cycles or until disease progression or unacceptable toxicity or consent withdrawal whichever occurs first
Research Site
Brescia, BS, Italy
Research Site
Florence, FI, Italy
Research Site
Genova, GE, Italy
Research Site
Progression Free Survival
Progression was defined as Time from the date of first dose of study medication to progression of disease, or death (it also includes patients who are lost to follow-up or have withdrawn consent) and evaluated with RECIST criteria as an increase of at least 20% in the sum of longest diameter (LD) of target lesion(s) taking as reference the smallest sum of LD since the treatment started or any new lesion(s).
Time frame: up to 1032 days
Objective Tumor Response Rate (CR+PR),
Objective Tumor Response Rate was defined as complete response (CR) + partial response (PR) evaluated by RECIST. CR was defined as disappearance of all target lesions. PR was defined as at least 30% decrease in the sum of longest diameters (LD) of target lesion(s) taking as reference the baseline sum of LD
Time frame: up to 1032 days
Disease Control Rate (CR+PR+SD)
DCR is the sum of patients with a best overall CR, PR or SD (\>=8 weeks) by the patient in the analysis
Time frame: up to 1032 days
Duration of Response (DOR)
DOR is defined from the date of first documentation of response until date of PD or death
Time frame: up to 1032 days
Overall Survival
OS is defined from the date of randomization to death
Time frame: up to 1032 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Placebo to match ZD6474 100 mg as a once daily oral dose, from Day 1 until disease progression or unacceptable toxicity or consent withdrawal whichever occurs first
Milan, Mi, Italy
Research Site
Palermo, PA, Italy
Research Site
Aviano, PN, Italy
Research Site
Parma, PR, Italy
Research Site
Reggio Emilia, RE, Italy
Research Site
Ancona, Italy
Research Site
Livorno, Italy
...and 5 more locations