The FDA has raised safety concerns about GSK’s new drug for multiple myeloma. The agency’s questions focus on potential side effects that could impact patient safety. GSK must address these issues to move forward with the drug’s approval process. This development could delay the drug’s market entry, affecting GSK’s strategy and financial projections. The scrutiny highlights the FDA’s rigorous standards for new treatments, ensuring patient safety remains a top priority. GSK will need to provide additional data or modify the drug’s profile to meet regulatory requirements. The outcome will influence GSK’s position in the competitive oncology market.
FDA Raises Concerns on GSK Drug Safety
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