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CTTI

Clinical Trials Transformation Initiative

Study Design

Diuretic Comparison Project Case Example: Learning from an Integrated Health System

Posted on December 14, 2022February 5, 2025 by Hannah Faulkner

Diuretic Comparison Project Case Example: Learning from an Integrated Health System

Posted in Data Collecting and Reporting, Fully Integrated, Innovative Trials, Resources, Site Planning, Study Design, Study Operations, Trials in Clinical Practice, Trials in Clinical Practice

I-SPY Trial Case Example: Using an Embedded Trial to Identify New Treatments for Breast Cancer

Posted on December 14, 2022February 5, 2025 by Hannah Faulkner

I-SPY Trial Case Example: Using an Embedded Trial to Identify New Treatments for Breast Cancer

Posted in Data Collecting and Reporting, Fully Integrated, Innovative Trials, Resources, Site Planning, Study Design, Study Operations, Trials in Clinical Practice, Trials in Clinical Practice

RECOVERY Trial Case Example: Using an Embedded Trial to Identify Treatments for COVID-19

Posted on December 14, 2022February 5, 2025 by Hannah Faulkner

RECOVERY Trial Case Example: Using an Embedded Trial to Identify Treatments for COVID-19

Posted in Data Collecting and Reporting, Fully Integrated, Innovative Trials, Resources, Site Planning, Study Design, Study Operations, Trials in Clinical Practice, Trials in Clinical Practice

Embedding Clinical Trial Elements into Clinical Practice

Posted on December 14, 2022February 5, 2025 by Hannah Faulkner

Embedding Clinical Trial Elements into Clinical Practice

Posted in Data Collecting and Reporting, Fully Integrated, Innovative Trials, Recommendations, Site Planning, Study Design, Study Operations, Trials in Clinical Practice, Trials in Clinical Practice

Mobilizing the Clinical Trial Ecosystem to Drive Adoption of Master Protocols

Posted on September 9, 2022February 6, 2025 by Hannah Faulkner

Mobilizing the Clinical Trial Ecosystem to Drive Adoption of Master Protocols

Posted in Innovative Trials, Master Protocol Studies, Master Protocols, Publications, Related: Master Protocol Studies, Study Design, Study Operations

Accelerating eConsent Adoption During COVID-19

Posted on August 10, 2022February 21, 2025 by Hannah Faulkner

Accelerating eConsent Adoption During COVID-19

Posted in Access to Clinical Trials, Case Studies, COVID 19, COVID-19, Decentralized Trials, Ensuring Quality, Innovative Trials, Patient Engagement, Planning Decentralized Trials, Regulatory Submissions + Approvals, Site Planning, Study Design, Study Operations

CTTI Considerations for Advancing the Use of Digital Technologies for Data Capture & Improved Clinical Trials

Posted on June 9, 2022February 11, 2025 by Hannah Faulkner

CTTI Considerations for Advancing the Use of Digital Technologies for Data Capture & Improved Clinical Trials

Posted in Data Collecting and Reporting, Digital Health Technologies, Innovative Trials, Managing Data, Managing Data, Resources, Selecting and Testing Digital Health Technology, Study Design, Study Operations

Regulatory Engagement Opportunities when Developing Digitally Derived Endpoints

Posted on April 6, 2022February 5, 2025 by Hannah Faulkner

Regulatory Engagement Opportunities when Developing Digitally Derived Endpoints

Posted in Developing Novel Endpoints, Innovative Trials, Interacting with Regulators, Interacting with Regulators, Leveraging All Data, Regulatory Submissions + Approvals, Resources, Study Design

Question Bank for Identifying Meaningful Outcome Measures

Posted on April 5, 2022January 31, 2025 by Hannah Faulkner

Question Bank for Identifying Meaningful Outcome Measures

Posted in Developing Novel Endpoints, Innovative Trials, Leveraging All Data, Novel Endpoints, Regulatory Submissions + Approvals, Resources, Study Design, Study Operations

Preparing a Digitally-derived Endpoint for Key Endpoint Use

Posted on April 5, 2022January 31, 2025 by Hannah Faulkner

Preparing a Digitally-derived Endpoint for Key Endpoint Use

Posted in Developing Novel Endpoints, Innovative Trials, Leveraging All Data, Novel Endpoints, Regulatory Submissions + Approvals, Resources, Study Design, Study Operations

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