FDA
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The fatal monkeypox outbreak is re-emerging, are the investigational drugs proven to be ineffective?
DrugTime team will follow up on this key subject. Please stay tuned
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Celine Dion, the legendary pop diva, is waiting for a CAR-T therapy?
All our best wishes! We will continue to provide our assistance to drug discovery and development with full effort
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19款FDA批准的基因疗法
根据2024年7月12日CBER主任Peter Marks博士的演讲和公开信息准备
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秀发重回！FDA批准的「斑秃」新药，安全性怎么样？
2024年7月25日，印度第一大制药公司Sun Pharmaceutical 宣布FDA批准了Leqselvi（deuruxolitinib）一日两次8mg片剂用于治疗成人重度斑秃…
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How to Maximize the Value of Innovative Drugs When Going Global? Former FDA and EMA Experts from Parexel Reveal the Best Plan
13 seasoned experts shared rather valuable information for 4 hours
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Sarepta Therapeutics Announces Expanded US FDA Approval of ELEVIDYS to Duchenne Muscular Dystrophy Patients Ages 4 and Above
Congratulations to Sarepta Therapeutics and DMD patients!
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Day One Announces Sale of Priority Review Voucher for $108 Million
Congratulations to Day One Biopharmaceuticals!
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CAR-T Black Box Warning Controversy Again？
DrugTimes will follow this crucial matter and report timely
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FDA的“圣诞节礼物”，印度裔杰青的首个FDA批准
《我和我的药时代》| 医药版《我和我的祖国》（诚聘歌手演唱） 印象中，每年的圣诞节前夕，美国食品药品监督管理局（FDA）都会多批准几款药物，作为送给药企和患者的“圣诞…
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前线治疗获批上市！FDA批准XPOVIO®用于治疗接受过至少一线治疗的多发性骨髓瘤患者
口服XPOVIO®作为联用疗法，获批用于既往接受过至少一线治疗的多发性骨髓瘤患者，显著扩展了XPOVIO®可治疗的患者群体 口服XPOVIO®是目前唯一一种获批联合硼替佐米（每周一…
