Reported Saturday, Nuvation Bio Announces Pooled Data From TRUST-I And TRUST-II Studies, Highlighting Taletrectinib's Best-In-Class Potential For Advanced ROS1-Positive NSCLC
Portfolio Pulse from Benzinga Newsdesk
Nuvation Bio announced promising pooled data from TRUST-I and TRUST-II studies for taletrectinib, showing significant tumor shrinkage in advanced ROS1-positive NSCLC patients. The drug demonstrated durable responses, prolonged progression-free survival, and a favorable safety profile. Nuvation Bio plans to submit a New Drug Application to the FDA in Q4 2024.
September 16, 2024 | 8:51 am
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POSITIVE IMPACT
Nuvation Bio's taletrectinib shows strong potential in treating advanced ROS1-positive NSCLC, with high tumor shrinkage rates and durable responses. The company plans to submit an NDA to the FDA in Q4 2024, which could significantly impact its stock price.
The positive results from the TRUST-I and TRUST-II studies highlight taletrectinib's efficacy and safety, which are critical for FDA approval. The planned NDA submission in Q4 2024 is a significant milestone that could lead to market approval, potentially boosting Nuvation Bio's stock price.
CONFIDENCE 95
IMPORTANCE 90
RELEVANCE 100