A Multicenter, Multinational, Randomized, Open-Label, Parallel-Group Trial to Evaluate hte Safety of Fentanyl TAIFUN Treatment after titrated Dose Administration and the Current Breakthrough Pain Treatment for Breakthrough Pain in Cancer Patients on Maintenance Opioid Therapy
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
500
Inhalation of Fentanyl via TAIFUN inhaler
Current optimized BTP treatment
NZOZ
Włocławek, Wolnosc, Poland
RECRUITINGAE Profile
Time frame: 28 Days
To characterize the safety of Fentanyl TAIFUN treatment vs. the current BTP treatment based on the AE profile
Time frame: 28 days
To estimate the proportion of patients taht can be titrated to an effective dose of Fentanyl TAIFUN
Time frame: 28 Days
To evaluate the efficacy of Fentanyl TAIFUN with the titrated dose and the current BTP treatment with the confirmed dose
Time frame: 28 Days
To evaluate patients's preference between Fentanyl TAIFUN and the baseline BTP medication
Time frame: 28 Days
To evaluate the sustained analgesic effect of Fentanyl TAIFUN and the current BTP treatment
Time frame: 28 Days
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