Methods and systems for predictive clinical planning and design and integrated execution services
First Claim
1. A computer-implemented method comprising:
- displaying a graphical user interface on one or more display screens, the graphical user interface providing a graphical representation of at least a portion of a clinical trial and comprising a plurality of graphical nodes, the plurality of graphical nodes comprising;
a central node;
one or more first child nodes directly connected to the central node, each of the child nodes representing aspects of the clinical trial;
one or more second child nodes, each of the one or more second child nodes directly connected to one of a first child node or a second child node and indirectly connected to the central node, each of the second child nodes representing a sub-node of the respective directly connected node, andwherein at least one of the first or second child nodes is associated with an editor configured to enable modification of one or more parameters associated with the respective first or second child node;
accessing a database to retrieve information associated with the clinical trial;
retrieving information from the database, the information associated with the first child nodes and the second child nodes;
propagating the information through the child nodes to the central node; and
displaying summary information about the clinical trial based on the propagated information.
8 Assignments
0 Petitions
Accused Products
Abstract
Systems and methods for predictive clinical planning, design, and integrated execution services are provided. The system may comprise a database, a web server, an application server, and a client.
The system may be used to develop a strategic map of a proposed clinical plan, wherein the clinical plan may include a draft launch label attribute, one or more strategies, and a schema; linking the clinical plan and schema to one or more trials; subsequently linking the trials to one or more objectives and measures; subsequently linking none, one, or a plurality of objectives to none, one, or a plurality of measures; identifying patient criteria and enrolling patients from one or more investigator sites located in one or more countries; and integrating the clinical plan with a clinical plan execution application.
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Citations
21 Claims
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1. A computer-implemented method comprising:
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displaying a graphical user interface on one or more display screens, the graphical user interface providing a graphical representation of at least a portion of a clinical trial and comprising a plurality of graphical nodes, the plurality of graphical nodes comprising; a central node; one or more first child nodes directly connected to the central node, each of the child nodes representing aspects of the clinical trial; one or more second child nodes, each of the one or more second child nodes directly connected to one of a first child node or a second child node and indirectly connected to the central node, each of the second child nodes representing a sub-node of the respective directly connected node, and wherein at least one of the first or second child nodes is associated with an editor configured to enable modification of one or more parameters associated with the respective first or second child node; accessing a database to retrieve information associated with the clinical trial; retrieving information from the database, the information associated with the first child nodes and the second child nodes; propagating the information through the child nodes to the central node; and displaying summary information about the clinical trial based on the propagated information. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10)
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11. A non-transitory computer-readable medium comprising processor-executable program code configured to cause a processor to:
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display a graphical user interface on one or more display screens, the graphical user interface providing a graphical representation of at least a portion of a clinical trial and comprising a plurality of graphical nodes, the plurality of graphical nodes comprising; a central node; one or more first child nodes directly connected to the central node, each of the child nodes representing aspects of the clinical trial; one or more second child nodes, each of the one or more second child nodes directly connected to one of a first child node or a second child node and indirectly connected to the central node, each of the second child nodes representing a sub-node of the respective directly connected node, and wherein at least one of the first or second child nodes is associated with an editor configured to enable modification of one or more parameters associated with the respective first or second child node; access a database to retrieve information associated with the clinical trial; retrieve information from the database, the information associated with the first child nodes and the second child nodes; propagate the information through the child nodes to the central node; and display summary information about the clinical trial based on the propagated information. - View Dependent Claims (12, 13, 14, 15, 16, 17, 18, 19, 20)
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21. A system, comprising:
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a non-transitory computer-readable medium; and a processor in communication with the non-transitory computer readable medium configured to; display a graphical user interface on one or more display screens, the graphical user interface providing a graphical representation of at least a portion of a clinical trial and comprising a plurality of graphical nodes, the plurality of graphical nodes comprising; a central node; one or more first child nodes directly connected to the central node, each of the child nodes representing aspects of the clinical trial; one or more second child nodes, each of the one or more second child nodes directly connected to one of a first child node or a second child node and indirectly connected to the central node, each of the second child nodes representing a sub-node of the respective directly connected node, and wherein at least one of the first or second child nodes is associated with an editor configured to enable modification of one or more parameters associated with the respective first or second child node; access a database to retrieve information associated with the clinical trial; retrieve information from the database, the information associated with the first child nodes and the second child nodes; propagate the information through the child nodes to the central node; and display summary information about the clinical trial based on the propagated information.
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Specification