DUO-E Clinical Trial: Treatment and Randomization

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10 Questions

What is the primary objective of the DUO-E clinical trial?

To evaluate the efficacy and safety of first-line durvalumab + platinum-based chemotherapy followed by maintenance durvalumab ± olaparib

What is the dual primary endpoint of the DUO-E clinical trial?

Investigator-assessed progression-free survival (PFS) for durvalumab only arm vs placebo arm, and durvalumab + olaparib arm vs placebo arm

What is the treatment regimen being evaluated in the DUO-E clinical trial?

First-line platinum-based chemotherapy followed by maintenance durvalumab ± olaparib

What is the patient population being studied in the DUO-E clinical trial?

Patients with newly diagnosed advanced or recurrent EC

What is the role of olaparib in the DUO-E clinical trial?

As a maintenance therapy in combination with durvalumab

What is the purpose of the investigator-assessed progression-free survival (PFS) endpoint in the DUO-E clinical trial?

To compare the efficacy of durvalumab with and without olaparib

What is the significance of the placebo arm in the DUO-E clinical trial?

It serves as a comparator arm to evaluate the efficacy of durvalumab + olaparib

What is the role of carboplatin/paclitaxel in the DUO-E clinical trial?

As a platinum-based chemotherapy agent in combination with durvalumab

What is the significance of the maintenance phase in the DUO-E clinical trial?

It evaluates the efficacy of durvalumab ± olaparib after initial treatment with platinum-based chemotherapy

What is the scope of the DUO-E clinical trial?

A phase III trial evaluating the efficacy and safety of durvalumab + platinum-based chemotherapy followed by maintenance durvalumab ± olaparib in patients with newly diagnosed advanced or recurrent EC

This quiz assesses your understanding of the DUO-E clinical trial, including treatment duration, cycles, and randomization. It covers the different arms of the trial, including the placebo arm, durvalumab only arm, and carboplatin/paclitaxel arms. Test your knowledge of the trial's design and treatment protocols.

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