Application of a Novel Endpoint Staging Framework: Proof of Concept in the AMBAR Study
Background: A theoretical endpoint staging framework was previously developed and published, aligning outcomes (i.e., memory) to the stage of Alzheimer’s disease (AD) in which a given outcome is most relevant (i.e., has the greatest risk of degradation). The framework guides the selection of endpoin...
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Published in | Journal of Alzheimer's disease Vol. 98; no. 3; pp. 1079 - 1094 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London, England
SAGE Publications
02.04.2024
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Subjects | |
Online Access | Get full text |
ISSN | 1387-2877 1875-8908 |
DOI | 10.3233/JAD-231197 |
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Abstract | Background:
A theoretical endpoint staging framework was previously developed and published, aligning outcomes (i.e., memory) to the stage of Alzheimer’s disease (AD) in which a given outcome is most relevant (i.e., has the greatest risk of degradation). The framework guides the selection of endpoints measuring outcomes relevant within a target AD population. Here, a proof of concept is presented via post-hoc analyses of the Alzheimer Management by Albumin Replacement (AMBAR) Phase 2b clinical trial in patients with AD (NCT01561053, 2012).
Objective:
To evaluate whether aligning endpoints measuring cognition, function, and quality of life to hypothesized ‘target’ stages of AD yields magnitudes of treatment efficacy greater than those reported in the AMBAR full analysis set (FAS).
Methods:
Three endpoints were tested: ADAS-Cog 12, ADCS-ADL, and QoL-AD. The magnitude of treatment efficacy was hypothesized to be maximized in the target stages of mild, mild-to-moderate, and very mild AD, respectively, compared to the full analysis set (FAS) and non-target stages.
Results:
For ADAS-Cog 12, the magnitude of treatment efficacy was largest in the non-target stage (–4.0, p = 0.0760) compared to target stage and FAS. For ADCS-ADL and QoL-AD, the magnitude of treatment efficacy was largest in the target stage (14.2, p = 0.0003; 2.4, p < 0.0001, respectively) compared to non-target stage and FAS.
Conclusions:
Findings indicated that evaluating endpoints in the most relevant AD stage can increase the magnitude of the observed treatment efficacy. Evidence provides preliminary proof of concept for the endpoint staging framework. |
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AbstractList | A theoretical endpoint staging framework was previously developed and published, aligning outcomes (i.e., memory) to the stage of Alzheimer's disease (AD) in which a given outcome is most relevant (i.e., has the greatest risk of degradation). The framework guides the selection of endpoints measuring outcomes relevant within a target AD population. Here, a proof of concept is presented via post-hoc analyses of the Alzheimer Management by Albumin Replacement (AMBAR) Phase 2b clinical trial in patients with AD (NCT01561053, 2012).
To evaluate whether aligning endpoints measuring cognition, function, and quality of life to hypothesized 'target' stages of AD yields magnitudes of treatment efficacy greater than those reported in the AMBAR full analysis set (FAS).
Three endpoints were tested: ADAS-Cog 12, ADCS-ADL, and QoL-AD. The magnitude of treatment efficacy was hypothesized to be maximized in the target stages of mild, mild-to-moderate, and very mild AD, respectively, compared to the full analysis set (FAS) and non-target stages.
For ADAS-Cog 12, the magnitude of treatment efficacy was largest in the non-target stage (-4.0, p = 0.0760) compared to target stage and FAS. For ADCS-ADL and QoL-AD, the magnitude of treatment efficacy was largest in the target stage (14.2, p = 0.0003; 2.4, p < 0.0001, respectively) compared to non-target stage and FAS.
Findings indicated that evaluating endpoints in the most relevant AD stage can increase the magnitude of the observed treatment efficacy. Evidence provides preliminary proof of concept for the endpoint staging framework. Background: A theoretical endpoint staging framework was previously developed and published, aligning outcomes (i.e., memory) to the stage of Alzheimer’s disease (AD) in which a given outcome is most relevant (i.e., has the greatest risk of degradation). The framework guides the selection of endpoints measuring outcomes relevant within a target AD population. Here, a proof of concept is presented via post-hoc analyses of the Alzheimer Management by Albumin Replacement (AMBAR) Phase 2b clinical trial in patients with AD (NCT01561053, 2012). Objective: To evaluate whether aligning endpoints measuring cognition, function, and quality of life to hypothesized ‘target’ stages of AD yields magnitudes of treatment efficacy greater than those reported in the AMBAR full analysis set (FAS). Methods: Three endpoints were tested: ADAS-Cog 12, ADCS-ADL, and QoL-AD. The magnitude of treatment efficacy was hypothesized to be maximized in the target stages of mild, mild-to-moderate, and very mild AD, respectively, compared to the full analysis set (FAS) and non-target stages. Results: For ADAS-Cog 12, the magnitude of treatment efficacy was largest in the non-target stage (–4.0, p = 0.0760) compared to target stage and FAS. For ADCS-ADL and QoL-AD, the magnitude of treatment efficacy was largest in the target stage (14.2, p = 0.0003; 2.4, p < 0.0001, respectively) compared to non-target stage and FAS. Conclusions: Findings indicated that evaluating endpoints in the most relevant AD stage can increase the magnitude of the observed treatment efficacy. Evidence provides preliminary proof of concept for the endpoint staging framework. |
Author | Davis, E. Anne Gomez-Ulloa, David Lipton, Richard B. Ayasse, Nicolai D. Barnes, Frederick B. Serrano, Daniel Runken, M. Chris Podger, Lauren Stewart, Walter F. |
Author_xml | – sequence: 1 givenname: Lauren surname: Podger fullname: Podger, Lauren email: laurenpodger@gmail.com organization: Grifols SSNA – sequence: 2 givenname: Walter F. surname: Stewart fullname: Stewart, Walter F. organization: Grifols SSNA – sequence: 3 givenname: Daniel surname: Serrano fullname: Serrano, Daniel organization: Grifols SSNA – sequence: 4 givenname: Richard B. surname: Lipton fullname: Lipton, Richard B. organization: Grifols SSNA – sequence: 5 givenname: David surname: Gomez-Ulloa fullname: Gomez-Ulloa, David organization: Grifols SSNA – sequence: 6 givenname: Nicolai D. surname: Ayasse fullname: Ayasse, Nicolai D. organization: Grifols SSNA – sequence: 7 givenname: Frederick B. surname: Barnes fullname: Barnes, Frederick B. organization: Grifols SSNA – sequence: 8 givenname: E. Anne surname: Davis fullname: Davis, E. Anne organization: Grifols SSNA – sequence: 9 givenname: M. Chris surname: Runken fullname: Runken, M. Chris organization: Grifols SSNA |
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Keywords | AMBAR Alzheimer’s disease cognition endpoint staging framework outcome measures function trial endpoints quality of life |
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Snippet | Background:
A theoretical endpoint staging framework was previously developed and published, aligning outcomes (i.e., memory) to the stage of Alzheimer’s... A theoretical endpoint staging framework was previously developed and published, aligning outcomes (i.e., memory) to the stage of Alzheimer's disease (AD) in... |
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Title | Application of a Novel Endpoint Staging Framework: Proof of Concept in the AMBAR Study |
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