Introduction New treatments for neurodegenerative disease are urgently needed, and clinical trial methods are an essential component of new drug development. Although a parallel-group study design for neurological disorder clinical trials is commonly used to test the effectiveness of a new treatment as compared to placebo, it does not efficiently use information from the on-going study to increase the success rate of a trial or to stop a trial earlier when the new treatment is indeed ineffective. Methods We review some recent advances in designs for clinical trials, including futility designs and adaptive designs. Results Futility designs and noninferiority designs are used to test the nonsuperiority and the noninferiority of a new treatmen...
Adaptive designs for clinical trials permit alterations to a study in response to accumulating data ...
The aim of the thesis is to investigate how to optimize the design and analysis of randomized and no...
With current success rates of confirmatory studies being only around 50%, new approaches to drug dev...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Adaptive designs have the potential to improve efficiency in the evaluation of new medical treatment...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Objectives: Clinical trials in neurodegenerative disorders are facing high futility rates and rising...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Numerous human medical problems or diseases have been aided by the development of effective treatmen...
Objectives: Clinical trials are complicated, expensive, time-consuming, and frequently do not lead t...
Adaptive designs for clinical trials permit alterations to a study in response to accumulating data ...
The recent advances in the development of potentially disease modifying cell and gene therapies for ...
Background: In an adaptive trial, the researcher may have the option of responding to interim safet...
Adaptive designs can make clinical trials more flexible by utilising results accumulating in the tri...
Adaptive designs for clinical trials permit alterations to a study in response to accumulating data ...
The aim of the thesis is to investigate how to optimize the design and analysis of randomized and no...
With current success rates of confirmatory studies being only around 50%, new approaches to drug dev...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Adaptive designs have the potential to improve efficiency in the evaluation of new medical treatment...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Objectives: Clinical trials in neurodegenerative disorders are facing high futility rates and rising...
Clinical trials may apply or use a sequential introduction of a new treatment to determine its effic...
Numerous human medical problems or diseases have been aided by the development of effective treatmen...
Objectives: Clinical trials are complicated, expensive, time-consuming, and frequently do not lead t...
Adaptive designs for clinical trials permit alterations to a study in response to accumulating data ...
The recent advances in the development of potentially disease modifying cell and gene therapies for ...
Background: In an adaptive trial, the researcher may have the option of responding to interim safet...
Adaptive designs can make clinical trials more flexible by utilising results accumulating in the tri...
Adaptive designs for clinical trials permit alterations to a study in response to accumulating data ...
The aim of the thesis is to investigate how to optimize the design and analysis of randomized and no...
With current success rates of confirmatory studies being only around 50%, new approaches to drug dev...