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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
Jun 11,2024
Medicilon helps Sungening Biological's first innovative drug SG1001 oral tablet obtain IND approval in China
Recently, Sungening Biological's (Sungening) first innovative drug SG1001 successfully obtained the implicit clinical trial approval from the National Medical Products Administration (Acceptance Number: CXHL2400203).
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Medicilon helps Sungening Biological's first innovative drug SG1001 oral tablet obtain IND approval in China
Jun 11,2024
Medicilon assists the world's first, Leado Pharma's IBD treatment FIC new drug IND application approved by the US FDA
On May 11, Leado Pharma (Leado) announced that the company's independently developed First-in-class new drug LD09163 tablets for treating inflammatory bowel disease has obtained IND approval from the US FDA and officially entered the clinical development stage.
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Medicilon assists the world's first, Leado Pharma's IBD treatment FIC new drug IND application approved by the US FDA
Jun 11,2024
Medicilon congratulates - Treatable and Accessible! Adult and adolescent Type A and Type B influenza! AnDiCon Bio's pill cures influenza with the new drug Madoxanavir - Phase III successful research
Medicilon, as a partner of AnDiCon, provided formulation research services for the 'pediatric version' of the anti-influenza Class 1 Madoxanavir granules for influenza, assisting in its rapid advancement in preclinical research and development processes.
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Medicilon congratulates - Treatable and Accessible! Adult and adolescent Type A and Type B influenza! AnDiCon Bio's pill cures influenza with the new drug Madoxanavir - Phase III successful research
Mar 19,2024
Medicilon assists Biotime obtain approval for its first dual-filing innovative drug in China and the United States
Shanghai Medicilon Inc. (Medicilon) provides one-stop preclinical R&D services from target to IND application for the research and development of BIOT-001, and fully empowers BIOT-001 tablets to obtain the approval in China and United States.
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Medicilon assists Biotime obtain approval for its first dual-filing innovative drug in China and the United States