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Ponezumab in mild-t...
Ponezumab in mild-to-moderate Alzheimer's disease : Randomized phase II PET-PIB study
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- Landen, Jaren W. (författare)
- Pfizer Inc. US
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- Andreasen, Niels (författare)
- Karolinska University Hospital
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- Cronenberger, Carol L. (författare)
- Pfizer Inc. US
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- Schwartz, Pamela F. (författare)
- Pfizer Inc. US
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- Börjesson-Hanson, Anne (författare)
- Sahlgrenska University Hospital
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- Östlund, Henrik (författare)
- Lund University,Lunds universitet,Klinisk minnesforskning,Forskargrupper vid Lunds universitet,Clinical Memory Research,Lund University Research Groups
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- Sattler, Catherine A. (författare)
- Pfizer Inc. US
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- Binneman, Brendon (författare)
- Pfizer Inc. US
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- Bednar, Martin M. (författare)
- Pfizer Inc. US
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Pfizer Inc US Karolinska University Hospital (creator_code:org_t)
- 2017-06-08
- 2017
- Engelska 9 s.
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Ingår i: Alzheimer's and Dementia: Translational Research and Clinical Interventions. - : Wiley. - 2352-8737. ; 3:3, s. 393-401
- Relaterad länk:
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http://dx.doi.org/10...
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https://doi.org/10.1...
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https://lup.lub.lu.s...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Introduction The safety, pharmacokinetics, and effect on peripheral and central amyloid β (Aβ) of multiple doses of ponezumab, an anti-Aβ monoclonal antibody, were characterized in subjects with mild-to-moderate Alzheimer's disease treated for 1 year. Methods Subjects were aged ≥50 years with Mini–Mental State Examination scores 16 to 26. Cohort Q was randomized to ponezumab 10 mg/kg (n = 12) or placebo (n = 6) quarterly. Cohort M was randomized to a loading dose of ponezumab 10 mg/kg or placebo, followed by monthly ponezumab 7.5 mg/kg (n = 12) or placebo (n = 6), respectively. Results Ponezumab was generally well tolerated. Plasma concentrations increased dose dependently, but cerebrospinal fluid (CSF) penetration was low. Plasma Aβ increased dose dependently with ponezumab, but CSF biomarkers, brain amyloid burden, cognition, and function were not affected. Conclusions Both ponezumab dosing schedules were generally safe and well tolerated but did not alter CSF biomarkers, brain amyloid burden, or clinical outcomes.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Neurologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Neurology (hsv//eng)
Nyckelord
- Alzheimer's disease
- Amyloid
- Anti-drug antibodies
- Antibody
- Pharmacodynamics
- Pharmacokinetics
- PIB
- Ponezumab
- Safety
- Tolerability
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
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