This is a double- blind, multicenter, randomized Phase II study to evaluate the efficacy and safety of AT-101 in combination with docetaxel in relapsed/refractory non-small cell lung cancer
Further Study Details provided by Ascenta.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
106
AT-101 30 mg bid on days 1, 2, and 3 of each 21 day cycle, docetaxel, 75 mg/m2 on day 1 of each 21 day cycle; until progression or unacceptable toxicity develops
placebo 3 tabs bid on days 1, 2, and 3 of each 21 day cycle, docetaxel, 75 mg/m2 on day 1 of each 21 day cycle; until progression or unacceptable toxicity develops
Research Site
Durham, North Carolina, United States
Research Site
Arkhangelsk, Russia
Research Site
Chelyabinsk, Russia
duration of disease remission
Time frame: 12 months
number of participants with adverse events
Time frame: 12 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Site
Kaliningrad, Russia
Research Site
Kazan', Russia
Research Site
Moscow, Russia
Research Sites (4)
Saint Petersburg, Russia
Research Site
Samara, Russia
Research Site
Stavropol, Russia
Research Site
Voronezh, Russia
...and 8 more locations