FDA Bristol Myers Squibb's Application For Subcutaneous Nivolumab (Nivolumab And Hyaluronidase), With Prescription Drug User Fee Act Goal Date Of February 28, 2025
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The FDA has accepted Bristol Myers Squibb's application for a subcutaneous form of Nivolumab, combined with Hyaluronidase, setting a Prescription Drug User Fee Act goal date of February 28, 2025.

May 06, 2024 | 11:01 am
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Bristol Myers Squibb's new drug application for a subcutaneous form of Nivolumab has been accepted by the FDA, with a review goal date set for February 28, 2025.
The acceptance of Bristol Myers Squibb's application by the FDA is a positive development, indicating progress in the drug's approval process. This could potentially lead to a new treatment option in the market, enhancing the company's product portfolio and possibly boosting investor confidence. The setting of a Prescription Drug User Fee Act goal date provides a clear timeline for the review process, which is generally viewed positively by the market.
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IMPORTANCE 90
RELEVANCE 100