-
1.
公开(公告)号:EP4440546A1
公开(公告)日:2024-10-09
申请号:EP22847214.8
申请日:2022-12-04
Applicant: Incyte Corporation
Inventor: MODEPALLI, Naresh , SHETH, Trupti , BROWN, Marc , EVANS, Charles , FIDGE, James , GUIDALI, Florencia , MCINTOSH, Tecashanell , COFRE, Vanessa
IPC: A61K9/00 , A61K9/107 , A61K9/113 , A61K9/70 , A61K47/10 , A61K47/18 , A61K31/4155 , A61K31/519 , A61P17/00 , A61P17/06 , A61P17/10 , A61P17/12 , A61P17/14
CPC classification number: A61K9/0014 , A61K47/18 , A61K9/7015 , A61K9/107 , A61K47/10 , A61K31/519 , A61P17/00 , A61P17/06 , A61P17/10 , A61P17/12 , A61P17/14 , A61K9/0017 , A61K9/113
-
公开(公告)号:EP4431528A1
公开(公告)日:2024-09-18
申请号:EP21961862.6
申请日:2021-10-29
Applicant: Longbio Pharma (Suzhou) Co., Ltd.
Inventor: SUN, Nai-Chau , SUN, Chow-Rou-Yun , MA, Haili , LIU, Yunhua , YANG, Hongzhou , GUO, Ruowen , GAO, Qi , LIU, Heng
CPC classification number: A61K39/00 , A61K39/395 , A61K47/18 , A61P11/06 , A61P37/08 , C07K16/28 , C07K16/42 , C12N15/63
Abstract: The present application relates to an antigen binding protein comprising at least one CDR of a heavy chain variable region and at least one CDR of a light chain variable region, wherein said heavy chain variable region comprises an amino acid sequence as set forth in any one of SEQ ID NOs: 73 or 74, and the light chain variable region comprises an amino acid sequence as set forth in any one of SEQ ID NOs: 75 or 76.
-
公开(公告)号:EP4426347A1
公开(公告)日:2024-09-11
申请号:EP22814311.1
申请日:2022-11-04
Applicant: AstraZeneca UK Limited
Inventor: SCHMELZER, Albert , PATEL, Sajal , MEDINA, Annette , GALLEGOS, Austin
IPC: A61K39/395 , A61K31/00
CPC classification number: A61K39/39591 , A61K47/26 , A61K47/18 , A61K9/0019 , A61P37/00
-
公开(公告)号:EP4424313A1
公开(公告)日:2024-09-04
申请号:EP22887110.9
申请日:2022-10-27
Applicant: CHUGAI SEIYAKU KABUSHIKI KAISHA
Inventor: KANOH Takeo , TAKAHASHI Shodai , MAEDA Yuki , HASHIMOTO Shota
IPC: A61K31/5377 , A61K9/10 , A61K47/02 , A61K47/12 , A61K47/18 , A61K47/20 , A61K47/22 , A61K47/26 , A61K47/36 , A61K47/38 , A61K47/46 , A61P35/00 , A61P43/00
CPC classification number: A61P43/00 , A61K47/20 , A61K47/22 , A61K31/5377 , A61K9/10 , A61K47/02 , A61K47/46 , A61K47/12 , A61P35/00 , A61K47/26 , A61K47/36 , A61K47/38 , A61K47/18
Abstract: The present invention relates to a syrup containing alectinib or a salt thereof. The present invention provides a syrup containing alectinib or a salt thereof, which is a poorly water-soluble agent, and having improved fluidity and/or palatability. The syrup of the present invention has a plasma concentration profile equivalent to or greater than, or is biologically equivalent to, a capsule containing the same amount of alectinib or a salt thereof as the syrup, or has an enhanced oral bioavailability compared to a capsule containing the same amount of alectinib or a salt thereof as the syrup.
-
公开(公告)号:EP4395815A1
公开(公告)日:2024-07-10
申请号:EP22863830.0
申请日:2022-09-02
Applicant: Dr. Reddy's Laboratories Limited
Inventor: JAYARAMAN, Murali , K GOUD, Saisharan , ASHOK NANKAR, Sunil , NANATH, Maya , SIGIREDDI, Indra Kumar , AGGARWAL, Lovisha , KALIGATLA, Sireesha Goswamy , MARIKANTY, Ravi Kumar , S, Abirami , SIVALANKA, Giridhar , PENMETSA, Ravi Kiranmai , LABALA, Suman , INGALE, Mahesh , SARKAR, Puja , DESAI, Mayur Vijay , KIRAVE, Prathibha Chandrashekhar , SHINDE, Chetan Govindrao
CPC classification number: C07K2317/2120130101 , C07K2317/7620130101 , C07K2317/9420130101 , C07K16/2818 , A61K39/39591 , A61K47/18 , A61K47/12 , A61K47/26 , A61K47/183 , A61K9/08
-
公开(公告)号:EP4339212A3
公开(公告)日:2024-06-19
申请号:EP23206430.3
申请日:2010-07-28
Applicant: F. Hoffmann-La Roche AG
Inventor: ADLER, Michael , GRAUSCHOPF, Ulla , MAHLER, Hanns-Christian , STAUCH, Oliver Boris
IPC: A61K9/00 , A61K9/19 , A61K38/47 , A61K39/395 , A61K47/18 , A61K47/20 , A61K47/26 , A61K47/42 , A61P35/00 , A61P35/04 , C07K16/32
CPC classification number: A61K9/19 , A61K39/39591 , A61K47/18 , A61K47/183 , A61K47/26 , A61K47/42 , C07K16/32 , A61K9/0019 , A61K38/47 , C12Y302/01035 , A61K47/20 , A61P35/00 , A61P35/04
Abstract: The present invention relates to a highly concentrated, stable pharmaceutical formulation of a pharmaceutically active anti-HER2 antibody, such as e.g. Trastuzumab (HERCEPIN™), Pertuzumab or T-DM1, or a mixture of such antibody molecules for subcutaneous injection. In particular, the present invention relates to formulations comprising, in addition to a suitable amount of the anti-HER2 antibody, an effective amount of at least one hyaluronidase enzyme as a combined formulation or for use in form of a co-formulation. The said formulations comprise additionally at least one buffering agent, such as e.g. a histidine buffer, a stabilizer or a mixture of two or more stabilizers (e.g. a saccharide, such as e.g. α,α-trehalose dihydrate or sucrose, and optionally methionine as a second stabilizer), a nonionic surfactant and an effective amount of at least one hyaluronidase enzyme. Methods for preparing such formulations and their uses thereof are also provided.
-
公开(公告)号:EP4331681A3
公开(公告)日:2024-05-22
申请号:EP24150035.4
申请日:2019-03-14
Applicant: Kabushiki Kaisha Toshiba
Inventor: ISHIHARA, Mitsuko , AKAHOSHI, Eiichi , NAITO, Katsuyuki , NOZAKI, Emi , SARUWATARI, Saeko
IPC: A61P43/00
CPC classification number: A61K31/7088 , A61K31/7105 , A61K31/711 , A61K45/00 , A61K47/24 , A61K47/18 , A61K47/22 , A61K48/00 , A61P43/00 , C07C229/24 , C07D233/02 , C07D243/08 , C07D251/04 , C07D295/15 , C07D295/13 , C07D211/14 , C07D241/04 , A61K9/1272
Abstract: The present embodiment provides a method for delivering activators to cells, wherein said activator containing lipid particles are brought into contact with the cells,
where a compound represented by the formula (1):
Q-CHR2 (1)
wherein
Q is represented by the following formula (1-Q):
RQ12N-(CRQ22)q1-NRQ1-(CRQ22)q2-* (1-Q)
wherein
each RQ1 is independently an alkyl,
each RQ2 is independently hydrogen or an alkyl,
any two of RQ1s and RQ2s may link together to form a nitrogen-containing alicyclic ring,
q1 is an integer of 1 to 4,
q2 is an integer of 0 to 4, and
the mark * indicates the position bonding to -CHR2; and
each R is independently an aliphatic group of C12 to C24;
wherein said R is represented by the following formula (1-R):
-LR1-C(=O)-O-LR2 (1-R)
where
LR1 is alkylene and
LR2 is represented by the following formula (1-R2):
-CH2-CH=CH-(CH2)r2-H (1-R2)
where r2 is an integer of 1 to 10.-
公开(公告)号:EP4360652A2
公开(公告)日:2024-05-01
申请号:EP24160547.6
申请日:2017-11-03
Applicant: Takeda Pharmaceutical Company Limited
Inventor: FIEDLER, Christian , FRITSCHER, Eva , HASSLACHER, Meinhard , MITTERGRADNEGGER, Dominik , TABISH, Tanvir
IPC: A61K47/26
CPC classification number: A61K31/195 , A61K35/76 , A61P7/00 , A61K9/0019 , A61K9/19 , A61K47/183 , A61K47/22 , A61K47/26 , A61K47/02 , A61K47/18 , C12N15/86
Abstract: Adeno-associated liquid and lyophilized pharmaceutical compositions are provided herein. In exemplary aspects, the pharmaceutical compositions comprise about 5 mM to about 25 mM L-histidine, about 0 mM to about 150 mM sodium chloride, about 0.001 % (w/v) to about 0.01 % (w/v) polysorbate 80 (PS80), and about 1 % to about 10% (w/v) sucrose, trehalose, or combination thereof to AAV. In exemplary aspects, the pharmaceutical compositions further comprise glycine or mannitol. Methods of preparing a pharmaceutical composition comprising AAV, methods of treating a bleeding disorder in a subject, and methods of storing AAV compositions are also provided.
-
公开(公告)号:EP4360622A1
公开(公告)日:2024-05-01
申请号:EP22827682.0
申请日:2022-06-24
Applicant: Shanghai Aurora Biotechnology Co., Ltd.
Inventor: CHEN, Zhixiang , CHEN, Bangyin , LIU, Shuang , GUO, Zhen , FU, Jun , WANG, Tingting , YING, Shuhuan
IPC: A61K9/08 , A61K31/407 , A61K47/18 , A61P29/00
CPC classification number: A61P29/00 , A61K47/40 , A61K47/02 , A61K47/12 , A61K47/26 , A61K31/407 , A61K47/18 , A61K9/08
Abstract: A ketorolac liquid composition, a preparation method therefor, and an application thereof. Provided is a ketorolac liquid composition, comprising the following components: ketorolac tromethamine, a stabilizer, a buffer, an osmotic pressure regulator, and a pH regulator; the ketorolac liquid composition does not contain ethanol; a concentration of ketorolac tromethamine is 0.15 mmol/L-160.00 mmol/L, and the concentration refers to a ratio of a molar amount of the ketorolac tromethamine to a volume of the ketorolac liquid composition. The ketorolac liquid composition does not contain an organic solvent, has stable physical and chemical properties, has less in-vivo irritation, has a lower adverse reactions, is safer and more convenient, can improve medication compliance of patients and the convenience of clinical administration, and has good market prospects.
-
公开(公告)号:EP4056234B1
公开(公告)日:2024-04-17
申请号:EP21162437.4
申请日:2021-03-12
CPC classification number: A61K9/0043 , A61K9/006 , A61K47/20 , A61K47/18 , A61K9/08 , A61K9/007 , A61K33/30 , A61P31/14 , A61Q11/00 , A61K31/20 , A61K31/185 , A61K8/44 , A61K8/447 , A61K8/463 , A61K2800/59620130101
-
-
-
-
-
-
-
-
-