FDA Has Assigned A Standard Review And A Prescription Drug User Fee Act Action Date Of June 16, 2024 For Geron's New Drug Application For Imetelstat For Transfusion-dependent Anemia In Patients With Lower-risk Myelodysplastic Syndromes
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The FDA has assigned a standard review and a Prescription Drug User Fee Act action date of June 16, 2024, for Geron's new drug application for Imetelstat for transfusion-dependent anemia in patients with lower-risk myelodysplastic syndromes. The FDA also plans to hold an advisory committee meeting as part of the NDA review.
August 22, 2023 | 12:03 pm
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Geron's new drug application for Imetelstat has been assigned a review date by the FDA. This could potentially impact the company's stock in the short term.
The FDA's decision to assign a review date for Geron's new drug application is a significant step in the drug approval process. This news could potentially lead to increased investor confidence in Geron, which could positively impact the company's stock price in the short term.
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