Pemafibrate Dosing Regimens
    2.
    发明申请

    公开(公告)号:US20220296588A1

    公开(公告)日:2022-09-22

    申请号:US17708706

    申请日:2022-03-30

    IPC分类号: A61K31/496 A61K38/13

    摘要: To provide a medicament for safely treating a patient in need of treatment with pemafibrate, a salt thereof, or a solvate of any of these (hereinafter also referred to as pemafibrate therapy).
    A medicament for treating a patient in need of pemafibrate therapy, the medicament comprising the step of avoiding or suspending concomitant use of pemafibrate, a salt thereof, or a solvate of any of these as an active ingredient in order to suppress an increase in plasma concentration of pemafibrate when the treatment is combined with a medicament containing an OATP1B inhibitor, or the step of reducing the dose of pemafibrate, a salt thereof, or a solvate of any of these.

    Pharmaceutical preparation
    4.
    发明授权

    公开(公告)号:US11419855B2

    公开(公告)日:2022-08-23

    申请号:US16627058

    申请日:2018-06-29

    摘要: Provided is a novel technique for improving storage stability of a pharmaceutical composition containing pemafibrate, a salt thereof or a solvate thereof and a cellulose species. A pharmaceutical preparation obtained by storing a pharmaceutical composition containing the following components (A) and (B) in a tight package: (A) pemafibrate, a salt thereof or a solvate thereof; and (B) a cellulose species.

    Pemafibrate Dosing Regimens
    5.
    发明申请

    公开(公告)号:US20220257627A1

    公开(公告)日:2022-08-18

    申请号:US17708740

    申请日:2022-03-30

    摘要: To provide a medicament for safely treating a patient in need of treatment with pemafibrate, a salt thereof, or a solvate of any of these (hereinafter also referred to as pemafibrate therapy).
    A medicament for treating a patient in need of pemafibrate therapy, the medicament comprising the step of avoiding or suspending concomitant use of pemafibrate, a salt thereof, or a solvate of any of these as an active ingredient in order to suppress an increase in plasma concentration of pemafibrate when the treatment is combined with a medicament containing an OATP1B inhibitor, or the step of reducing the dose of pemafibrate, a salt thereof, or a solvate of any of these.

    Method for dynamic evaluation of tear fluid layer and device therefor

    公开(公告)号:US11369264B2

    公开(公告)日:2022-06-28

    申请号:US16637210

    申请日:2018-08-09

    摘要: A method for dynamically evaluating a tear fluid layer using an interference fringe image of the tear fluid layer composed of a plurality of consecutive frames, and includes: an image creation step of creating at least one break detection image of a first break detection image, a second break detection image, a third break detection image, and a fourth break detection image, which are images for detecting a breaking site of the tear fluid layer; a determination step of determining whether the break detection image created by the image creation step corresponds to a predetermined breakup pattern; a tally step of tallying the determination results determined by the determination step; and an evaluation step of evaluating, on the basis of a tallied result by the tally step, a breakup pattern of the interference fringe image of the tear fluid layer.

    Pharmaceutical composition
    7.
    发明授权

    公开(公告)号:US11344535B2

    公开(公告)日:2022-05-31

    申请号:US16627061

    申请日:2018-06-29

    摘要: Provided is a pharmaceutical composition containing pemafibrate, a salt thereof or a solvate thereof and having excellent storage stability. The pharmaceutical composition is provided to contain pemafibrate, a salt thereof or a solvate thereof, wherein a pH value of a solution produced by dissolving or dispersing the pharmaceutical composition in water is 7 or more.

    Method and device for evaluating tear fluid state

    公开(公告)号:US11266308B2

    公开(公告)日:2022-03-08

    申请号:US16306398

    申请日:2017-05-29

    发明人: Katsumi Yabusaki

    摘要: Provided are a method and a device for evaluating a tear fluid to objectively evaluate and determine the severity of dry eye or the like. Color information is acquired in a predetermined region of a tear fluid interference fringe image, a numerical value representing a color diversity is calculated from the color information acquired, and the numerical value representing the color diversity thus calculated is used as an index for evaluating a tear fluid state.

    Intraocular lens and manufacturing method thereof

    公开(公告)号:US11020219B2

    公开(公告)日:2021-06-01

    申请号:US16424051

    申请日:2019-05-28

    发明人: Asaki Suzaki

    摘要: Provided is an intraocular lens having a novel structure with high utility which is easy to adapt to patients, and can improve quality of vision (QOV). In an intraocular lens, an optical characteristic is set rotationally symmetric around an optical axis, and a spherical aberration of a size corresponding to a coma aberration remaining in a patient's eye after extraction of a human lens of the eye is set.