if Fda approved what will happen
If the FDA approves Lomecel-B for Alzheimer's disease, several significant outcomes can be expected:
1. **Market Launch**: Lomecel-B would become available for prescription, providing a new treatment option for patients with mild Alzheimer's disease, potentially impacting the estimated $15.9 billion Alzheimer's treatment market by 2030[1].
2. **Increased Stock Value**: Approval could lead to a substantial increase in Longeveron's stock price, as seen with previous FDA approvals in the biotech sector, reflecting investor confidence and market potential[3].
3. **Further Research and Development**: Approval may facilitate additional studies to explore Lomecel-B's efficacy in other indications, such as aging-related frailty and hypoplastic left heart syndrome, leveraging its regenerative properties[2][3].
4. **Regulatory Scrutiny**: Post-approval, Longeveron would face ongoing regulatory requirements and monitoring to ensure continued safety and efficacy of Lomecel-B in the market[3].
5. **Impact on Patients**: Successful treatment could improve cognitive function and quality of life for patients, addressing an urgent need in Alzheimer’s care[2].