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Generon Received US FDA Clearance to Initiate

Generon Received US FDA Clearance to Initiate Phase IIa Study With F-652, a First-in-Class Biologic, to Treat Patients With Acute GvHD

Generon Received US FDA Clearance to Initiate Phase IIa Study With F-652, a First-in-Class Biologic, to Treat Patients With Acute GvHD

バイオテクノロジーヘルスケア幹細胞腫瘍学臨床試験製薬　 TimeLine: a First-in-Class Biologic Generon Received US FDA Clearance to Initiate to Treat Patients With Acute GvHD

2015年05月04日