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HomeClient CenterMedicilon SupportIND 100
IND 100 Publications
Dec 09,2024
Medicilon Supports Partner Luye Pharma's LY09607 Clinical Trial Approval
Medicilon is proud to have supported Luye Pharmaceutical Co., Ltd. ("Luye Pharma") in securing clinical trial approval for LY09607, a new drug aimed at improving post-operative pain management.
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Medicilon Supports Partner Luye Pharma's LY09607 Clinical Trial Approval
Dec 09,2024
Medicilon Supports Jemincare's JMX-2002 Liposome Injection Clinical Trial Approval
Medicilon has been instrumental in advancing JMX-2002's development, providing comprehensive preclinical support through its specialized liposome drug development platform. This platform covers lipid synthesis, liposome preparation, formulation screening, safety evaluation, pharmacokinetics, and regulatory support, helping to optimize the drug's efficacy and safety profile.
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Medicilon Supports Jemincare's JMX-2002 Liposome Injection Clinical Trial Approval
Dec 03,2024
Medicilon Supports Partner Jemincare in Securing Clinical Approval for JM045 Sustained-Release Microspheres
Recently, JM045 sustained-release microspheres, independently developed by the Institute of Innovative Pharmaceuticals under Jemincare Pharmaceutical Group, received clinical trial approval. Medicilon provided pharmacokinetic studies and GLP-compliant safety evaluations for this development.
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Medicilon Supports Partner Jemincare in Securing Clinical Approval for JM045 Sustained-Release Microspheres
Nov 27,2024
Medicilon Partners with Hengrui Pharmaceuticals to Secure Clinical Approval for siRNA Drug HRS-9563
​HRS-9563, an innovative siRNA Class I drug developed by Shengdi Pharmaceuticals Co., Ltd., a subsidiary of Jiangsu Hengrui Pharmaceuticals Co., Ltd., has received clinical trial approval.
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Medicilon Partners with Hengrui Pharmaceuticals to Secure Clinical Approval for siRNA Drug HRS-9563
Oct 08,2024
Medicilon assists its partner Yayo Biotech in obtaining FDA approval for the IND application of the "YY2201 Tablets," a Class 1 new drug for advanced tumor
On September 14, Yayo Biotech received an FDA IND clinical approval (IND173030) for its independently developed Class 1 innovative drug, ATR kinase inhibitor YY2201 tablets. Medicilon, as a partner of Yayo Biotech, provided comprehensive R&D services for the development of YY2201 tablets.
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Medicilon assists its partner Yayo Biotech in obtaining FDA approval for the IND application of the "YY2201 Tablets," a Class 1 new drug for advanced tumor
Sep 18,2024
Medicilon congratulates Genfleet Therapeutics on the approval and launch of their KRAS G12C inhibitor, Fuzerelisib.
Recently, Genfleet Therapeutics launched its KRAS G12C inhibitor, Dabote® (Fuzerelisib Tablets, GFH925/IBI351). Shanghai Medicilon Inc. (Medicilon) leveraged its well-established pharmacokinetics research platform to provide early-stage animal pharmacokinetic services for Fuzerelisib.
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Medicilon congratulates Genfleet Therapeutics on the approval and launch of their KRAS G12C inhibitor, Fuzerelisib.
Sep 18,2024
Value repeatedly verified! Medicilon congratulates its partner, EpimAb Biotherapeutics, on the overseas authorization of their BCMA×CD3 bispecific antibody EMB-06
On September 4th, EpimAb Biotherapeutics (EpimAb) announced that it has reached a licensing agreement with Vignette Bio, Inc. (Vignette Bio) regarding EpimAb's BCMA-targeted T-cell engager (TCE) molecule, EMB-06. As a partner of EpimAb, Shanghai Medicilon Inc. (Medicilon) congratulates EpimAb on the licensing of its BCMA×CD3 bispecific antibody EMB-06 for international markets.
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Value repeatedly verified! Medicilon congratulates its partner, EpimAb Biotherapeutics, on the overseas authorization of their BCMA×CD3 bispecific antibody EMB-06
Sep 10,2024
Medicilon supports its partner Jingye Medicine & Chemical Co in obtaining approval for the market launch of its gadopentetate chemical raw material
Recently, Suzhou Jingye Medicine & Chemical Co., Ltd. (Jingye) successfully obtained the "Approval Notice for the Market Launch of Chemical Raw Materials" (Notice No. 2024YS00864) issued by the National Medical Products Administration (NMPA) for its gadopentetate chemical raw material.
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Medicilon supports its partner Jingye Medicine & Chemical Co in obtaining approval for the market launch of its gadopentetate chemical raw material
Jun 19,2024
Medicilon helps Keye Life's new drug targeting RNA helicase obtain dual approval in China and the United States
Medicilon provided efficacy studies and safety evaluation services that comply with both Chinese GLP and U.S. GLP standards for KY1, facilitating its successful dual IND approval in both China and the United States.
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Medicilon helps Keye Life's new drug targeting RNA helicase obtain dual approval in China and the United States
Jun 14,2024
Medicilon assists Insilico Medicine in obtaining approval for MAT2A inhibitor in both China and the United States
Recently, ISM3412, a class 1 new drug developed by InSilico Medicine Cayman TopCo (Insilico Medicine), received implied approval for clinical trials in China. As a strategic partner of Insilico Medicine, Medicilon provided preclinical research services for ISM3412, including pharmacokinetics and safety evaluation tests​.
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Medicilon assists Insilico Medicine in obtaining approval for MAT2A inhibitor in both China and the United States
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Email: marketing@medicilon.com

  

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