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Pharmacokinetic and Pharmacodynamic Effects of a ?-Secretase Modulator, PF-06648671, on CSF Amyloid-? Peptides in Randomized Phase I Studies.


ABSTRACT: ?-Secretase modulators (GSMs) represent a promising therapy for Alzheimer's disease by reducing pathogenic amyloid-? (A?) peptide production. Three phase I studies (NCT02316756, NCT02407353, and NCT02440100) investigated the safety/tolerability, pharmacokinetics (PKs), and pharmacodynamics (PDs) of the oral GSM, PF-06648671. A PK/PD indirect-response model was developed (using biomarker data) to simultaneously characterize differential effects of PF-06648671 on multiple A? species in cerebrospinal fluid (CSF). Healthy subjects (n = 120) received single doses or multiple-ascending doses of PF-06648671/placebo for 14 days. No serious adverse events occurred; severe adverse eventswere deemed not drug related. PF-06648671 decreased A?42 and A?40 concentrations in CSF, with greater effects on A?42, and increased A?37 and A?38 levels, particularly A?37. No significant change in total A? was observed. The PK/PD model well described the tendency of observed CSF A? data and the steady-state effects of PF-06648671, supporting its use for predicting central A? effects and optimal dose selection for GSMs in future trials.

SUBMITTER: Ahn JE 

PROVIDER: S-EPMC6977340 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Pharmacokinetic and Pharmacodynamic Effects of a γ-Secretase Modulator, PF-06648671, on CSF Amyloid-β Peptides in Randomized Phase I Studies.

Ahn Jae Eun JE   Carrieri Charles C   Dela Cruz Fernando F   Fullerton Terence T   Hajos-Korcsok Eva E   He Ping P   Kantaridis Constantino C   Leurent Claire C   Liu Richann R   Mancuso Jessica J   Mendes da Costa Laure L   Qiu Ruolun R  

Clinical pharmacology and therapeutics 20190911 1


γ-Secretase modulators (GSMs) represent a promising therapy for Alzheimer's disease by reducing pathogenic amyloid-β (Aβ) peptide production. Three phase I studies (NCT02316756, NCT02407353, and NCT02440100) investigated the safety/tolerability, pharmacokinetics (PKs), and pharmacodynamics (PDs) of the oral GSM, PF-06648671. A PK/PD indirect-response model was developed (using biomarker data) to simultaneously characterize differential effects of PF-06648671 on multiple Aβ species in cerebrospin  ...[more]

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