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New Data on Phase 1 Proposed Biosimilar Gan & Lee Insulins Aspart (GL-ASP), Lispro (GL-LIS), and Glargine (GL-GLA) Presented at the American Diabetes Association s 81st Scientific Sessions

New Data on Phase 1 Proposed Biosimilar Gan & Lee Insulins Aspart (GL-ASP), Lispro (GL-LIS), and Glargine (GL-GLA) Presented at the American Diabetes Association s 81st Scientific Sessions
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United statesKostenloser wertpapierhandelTim heiseEric zijlstraJia luGina antonucciScientific sessions of the american diabetes associationPrnewswire gan lee pharmaceuticals co ltdClinical sciencesScientific sessionsAmerican diabetes associationExecutive directorGanlee fineஒன்றுபட்டது மாநிலங்களில்ஜியா லுஜினா அன்டோனூசி

Gan & Lee receives EMA orphan drug designation for Phase I drug [ ] | Comunicati stampa CataniaOggi

06 aprile 2021 13:40 Fonte: Adnkronos #salute-e-benessere - BEIJING, and BRIDGEWATER, N.J., April 6, 2021 /PRNewswire/ Gan & Lee Pharmaceuticals Co., Ltd. (hereinafter referred to as Gan & Lee, stock code: 603087.SH), a global biopharmaceutical company, today announced that the European Medicine Agency (EMA) Committee for Orphan Medicinal Products granted orphan drug designation for the investigational compound GLR2007, for the treatment of glioma. Glioma is a broad term describing neuroepithelial tumors originating from glial cells of the central nervous system, including astrocytic tumors such as glioblastomas (GBM). GBM is one of the most aggressive primary brain tumors and has median survival of 12 to 15 months, despite advances in surgery, chemotherapy, and radiation therapy1. Gan & Lee s current clinical development program for GLR2007, a cyclin-dependent kinase 4/6 (CDK 4/6) inhibitor, is investigating the treatment of advanced solid tumors which has the potential

Gina antonucciMichelle mazuranicHead of global medical affairsCommittee for orphan medicinal productsGan lee pharmaceuticals co ltdEuropean unionHealth technology assessmentsEuropean commissionEuropean medicine agencyOrphan medicinal productsGlobal medical affairsOrphan medicinalGanlee fineஜினா அன்டோனூசிதலை ஆஃப் உலகளாவிய மருத்துவ வாழ்க்கைத்தொழில்கள்குழு க்கு ஆர்ஃபந் மருத்துவ ப்ராடக்ட்ஸ்

Gan & Lee receives EMA orphan drug designation for Phase I drug candidate GLR2007 for the treatment of glioma

Gan & Lee receives EMA orphan drug designation for Phase I drug candidate GLR2007 for the treatment of glioma USA - English Share this article Share this article BEIJING and BRIDGEWATER, N.J., April 6, 2021 /PRNewswire/ Gan & Lee Pharmaceuticals Co., Ltd. (hereinafter referred to as Gan & Lee, stock code: 603087.SH), a global biopharmaceutical company, today announced that the European Medicine Agency (EMA) Committee for Orphan Medicinal Products granted orphan drug designation for the investigational compound GLR2007, for the treatment of glioma. Glioma is a broad term describing neuroepithelial tumors originating from glial cells of the central nervous system, including astrocytic tumors such as glioblastomas (GBM). GBM is one of the most aggressive primary brain tumors and has median survival of 12 to 15 months, despite advances in surgery, chemotherapy, and radiation therapy

Gina antonucciMichelle mazuranicHead of global medical affairsCommittee for orphan medicinal productsGan lee pharmaceuticals co ltdEuropean unionHealth technology assessmentsEuropean commissionEuropean medicine agencyOrphan medicinal productsGlobal medical affairsOrphan medicinalGanlee fineஜினா அன்டோனூசிதலை ஆஃப் உலகளாவிய மருத்துவ வாழ்க்கைத்தொழில்கள்குழு க்கு ஆர்ஃபந் மருத்துவ ப்ராடக்ட்ஸ்