Organogenesis Provides Update on Second Phase 3 ReNu® Study

Core Insights - The second Phase 3 trial of ReNu did not achieve statistical significance for its primary endpoint, but showed a numerical improvement in pain reduction compared to the first Phase 3 trial [1][2][3] - The company plans to request a pre-BLA meeting with the FDA to discuss the submission pathway for ReNu, leveraging data from both Phase 3 trials [3][6] - ReNu has received FDA Regenerative Medicine Advanced Therapy (RMAT) designation, indicating its potential to address an unmet medical need in knee osteoarthritis [3][7] Study Results - The second Phase 3 trial involved 594 patients and demonstrated a baseline pain reduction of -6.9 for ReNu compared to -6.0 in the first Phase 3 trial [1][10] - The primary endpoint assessed the difference in knee pain reduction at six months using the WOMAC pain scale, with a numerical improvement of -0.5 favoring ReNu in the second trial [2][10] - The first Phase 3 trial achieved a statistically significant improvement of -0.7 favoring ReNu [2] Market Context - Knee osteoarthritis affects over 30 million Americans and is a leading cause of disability and poor quality of life [4] - The company believes that if approved, ReNu will meet a significant unmet medical need for patients suffering from symptomatic knee osteoarthritis [4][6]