Optimal and adaptive designs for multi-regional clinical trials with regional consistency requirement
To shorten the time for drug development and regulatory approval, a growing number of clinical trials are being conducted in multiple regions simultaneously. One of the challenges to multi-regional clinical trials (MRCT) is how to utilize the data obtained from other regions within the entire trial...
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| Language: | en_US |
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2016
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| Online Access: | https://hdl.handle.net/2144/15706 |