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GC Biopharma scores FDA nod for immunoglobulin therapy Alyglo

South Korea’s GC Biopharma Corp. has gained U.S. FDA approval for its immune-deficiency plasma drug, Alyglo (immune globulin intravenous, human-stwk; IVIG-SN 10%), five months after refiling its BLA, five months after refiling its BLA and before its PDUFA date of Jan. 13, 2024.

Global Biobetters Market is projected to reach US$ 99 2 Bn by the year 2029 at a 8 3% CAGR | Lower Dosage Frequency to drive market expansion |

Global Biobetters Market is projected to reach US$ 99 2 Bn by the year 2029 at a 8 3% CAGR | Lower Dosage Frequency to drive market expansion |
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Antithrombin Market Report 2023: Growing Active Pharmaceutical Ingredient Industry Bolsters Sector Expansion | Grifols

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