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公开(公告)号:US11918628B2
公开(公告)日:2024-03-05
申请号:US18355223
申请日:2023-07-19
发明人: Kennett Sprogøe , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
CPC分类号: A61K38/29 , A61K9/0019 , A61K9/1647 , A61K47/54 , A61K47/545 , A61K47/60 , A61K47/34
摘要: The present invention relates to a controlled-release parathyroid hormone (PTH) compound in which PTH(1-34) is reversibly conjugated to a branched polyethylene glycol. The invention further relates to a pharmaceutical composition of the compound. The compound or pharmaceutical composition is useful for treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH.
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公开(公告)号:US11857603B2
公开(公告)日:2024-01-02
申请号:US18053701
申请日:2022-11-08
发明人: Kennett Sprogøe , Lars Holten-Andersen , David Brian Karpf , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
摘要: The present invention relates to a pharmaceutical composition comprising a PTH compound, wherein after subcutaneous administration the pharmacokinetic profile of the PTH compound exhibits a peak to trough ratio of less than 4 within one injection interval.
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公开(公告)号:US20230321198A1
公开(公告)日:2023-10-12
申请号:US18176372
申请日:2023-02-28
发明人: Kennett Sprogøe , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
CPC分类号: A61K38/29 , A61K9/0019 , A61K9/1647 , A61K47/60 , A61K47/34
摘要: The present invention relates to a pharmaceutical composition comprising at least one controlled-release PTII compound or a pharmaceutically acceptable salt, hydrate or solvate thereof, for use in the treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH, pharmaceutical composition comprising at least one controlled-release PTII compound or a pharmaceutically acceptable salt, hydrate or solvate thereof, for use in the treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH, wherein said pharmaceutical composition is administered no more frequent than once every 24 hours with a dosage of the controlled-release PTH compound that corresponds to no more than 70% of the molar equivalent dose of PTII 1-84 administered every 24 hours required to maintain serum calcium within normal levels over said 24 hour period in humans.
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公开(公告)号:US20240173385A1
公开(公告)日:2024-05-30
申请号:US18496727
申请日:2023-10-27
发明人: Kennett Sprogøe , Lars Holten-Andersen , David Brian Karpf , Felix Cleenmann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
摘要: The present invention relates to a pharmaceutical composition comprising a PTH compound, wherein after subcutaneous administration the pharmacokinetic profile of the PTH compound exhibits a peak to trough ratio of less than 4 within one injection interval.
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公开(公告)号:US20240123038A1
公开(公告)日:2024-04-18
申请号:US18464046
申请日:2023-09-08
发明人: Kennett Sprogøe , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
CPC分类号: A61K38/29 , A61K9/0019 , A61K47/54 , A61K47/545 , A61K47/60
摘要: The present invention relates to PTH prodrugs, pharmaceutical compositions comprising such PTH prodrugs and their uses.
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公开(公告)号:US20230248836A1
公开(公告)日:2023-08-10
申请号:US18063294
申请日:2022-12-08
发明人: Kennett Sprogøe , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
CPC分类号: A61K47/60 , A61K47/54 , A61K47/545
摘要: The present invention relates to a pharmaceutical composition comprising at least one controlled-release PTH compound or a pharmaceutically acceptable salt, hydrate or solvate thereof, for use in the treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH, pharmaceutical composition comprising at least one controlled-release PTH compound or a pharmaceutically acceptable salt, hydrate or solvate thereof, for use in the treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH, wherein said pharmaceutical composition is administered no more frequent than once every 24 hours with a dosage of the controlled-release PTH compound that corresponds to no more than 70% of the molar equivalent dose of PTH 1-84 administered every 24 hours required to maintain serum calcium within normal levels over said 24 hour period in humans.
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公开(公告)号:US20210196801A1
公开(公告)日:2021-07-01
申请号:US17055695
申请日:2019-05-17
摘要: The present invention relates to a PTH conjugate, in which a PTH moiety is reversibly conjugated to a polymeric moiety or fatty acid-based moiety, or a pharmaceutically acceptable salt thereof or a pharmaceutical composition comprising said PTH conjugate or pharmaceutically acceptable salt thereof for use in the treatment, control, delay or prevention of a disease that can be treated, controlled, delayed or prevented with PTH, wherein the starting dose ranges from from 0.8 to 4.9 nmol/day and to the respective methods of treatment.
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公开(公告)号:US20230381284A1
公开(公告)日:2023-11-30
申请号:US18355223
申请日:2023-07-19
发明人: Kennett Sprogøe , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
CPC分类号: A61K38/29 , A61K9/0019 , A61K9/1647 , A61K47/60 , A61K47/545 , A61K47/54 , A61K47/34
摘要: The present invention relates to a pharmaceutical composition comprising at least one controlled-release PTH compound or a pharmaceutically acceptable salt, hydrate or solvate thereof, for use in the treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH, pharmaceutical composition comprising at least one controlled-release PTH compound or a pharmaceutically acceptable salt, hydrate or solvate thereof, for use in the treatment, control, delay or prevention of a condition that can be treated, controlled, delayed or prevented with PTH, wherein said pharmaceutical composition is administered no more frequent than once every 24 hours with a dosage of the controlled-release PTH compound that corresponds to no more than 70% of the molar equivalent dose of PTH 1-84 administered every 24 hours required to maintain serum calcium within normal levels over said 24 hour period in humans.
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公开(公告)号:US11793861B2
公开(公告)日:2023-10-24
申请号:US18053693
申请日:2022-11-08
发明人: Kennett Sprogøe , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
CPC分类号: A61K38/29 , A61K9/0019 , A61K47/54 , A61K47/545 , A61K47/60
摘要: The present invention relates to PTH prodrugs, pharmaceutical compositions comprising such PTH prodrugs and their uses.
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公开(公告)号:US11759504B2
公开(公告)日:2023-09-19
申请号:US16337955
申请日:2017-09-28
发明人: Kennett Sprogøe , Lars Holten-Andersen , David Brian Karpf , Felix Cleemann , Guillaume Maitro , Mathias Krusch , Thomas Wegge , Joachim Zettler
摘要: The present invention relates to a pharmaceutical composition comprising a PTH compound, wherein after subcutaneous administration the pharmacokinetic profile of the PTH compound exhibits a peak to trough ratio of less than 4 within one injection interval.
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