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GC Biopharma/Novel Pharma s Sanfilippo Syndrome Treatment Obtains FDA IND Clearance

GC Biopharma (006280. KS) and Novel Pharma have announced that the U.S. FDA has cleared the investigational new drug (IND) application for their jointly developed MPSIIIA (Sanfilippo Syndrome Type A) treatment, GC1130A..

United statesSouth koreaSoult ukpyolsiHeparann sulfataseSohee kimPharma sanfilippoRachel kimYelin junGc biopharma corpGreen cross corporationNovel pharma incNovel pharmaSanfilippo syndrome typeOrphan drug designationRare pediatric disease designationSyndrome type

GC Genome to Present New Clinical Data on Colorectal Cancer Detection at the ASCO Annual Meeting 2024

YONGIN, South Korea, May 7, 2024 /PRNewswire/ GC Genome Corporation, a leading diagnostics company, today announced that it will present the new clinical

San diegoUnited statesSouth koreaYelin junRachel kimSohee kimAmerican society of clinical oncologyGenece health incGc genome corporationJgc corpGc corporationClinical oncologyAnnual meetingPresentation detailsDevelopmental therapeuticsMolecularly targeted agents

GC Biopharma Presents Updates on its LSD Treatments at the WORLDSymposium 2024

GC Biopharma Presents Updates on its LSD Treatments at the WORLDSymposium 2024
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United statesSouth koreaSan diegoSouth koreanSeunghyun baekYelin junSohee kimRachel kimNobel pharmaEun chul huhGreen cross corporationChul huhLysosomal storage diseasesLysosomal diseasesMinute walk testOrphan drug designation

European Medicines Agency (EMA) Grants Orphan Drug Designation (ODD) to GC Biopharma s Treatment for Sanfilippo Syndrome (Type A)

/PRNewswire/ GC Biopharma Corp. (006280.KS) announced that the European Medicines Agency (EMA) has granted Orphan Drug Designation (ODD) to its.

South koreaYelin junRachel kimSohee kimEuropean medicines agencyGc biopharma corpPrnewswire gc biopharma corpGreen cross corporationOrphan drug designationEnzyme replacement therapySanfilippo syndromeRare pediatric diseaseNovel pharmaGc biopharmaHealth care amp hospitalsMedical pharmaceuticals

GC Biopharma Announces US FDA Approval for ALYGLO™ (Immune Globulin Intravenous, Human-stwk) 10% Liquid for Adults with Primary Humoral Immunodeficiency (PI)

/PRNewswire/ GC Biopharma Corp (006280.KS) today announces that the US Food and Drug Administration (FDA) has approved ALYGLO (immune globulin intravenous,.

United statesSouth koreaSelena perezSohee kimYelin junXia fxiaSeunghyun baekCation exchange chromatographyDrug administrationGc biopharma corpGc biopharma united states incAllergy associates of the palm beachesGreen cross corporationAllergy immunologistAllergy associatesPalm beaches