- Trevena Inc TRVN reported topline results from its post-approval study designed to assess the impact on cognitive function in subjects treated with Olinvyk compared to IV morphine.
- The FDA approved Olinvyk in 2020 indicated in adults for acute pain management.
- Olinvyk showed a statistically significant reduction in sedation versus IV morphine.
- Olinvyk showed a statistically significant difference or trend compared to IV morphine, despite the relatively small sample size, across a range of neurocognitive measures and motor performance.
- Other secondary outcome measures, including visual tracking and higher-order cognitive processing, did not show statistical differences between Olinvyk and IV morphine.
- No serious adverse events were observed in the study, and adverse events were generally assessed as mild.
- The company implemented a ~25% reduction in full-time employees and terminated its contract sales force agreement with Syneos to help reduce operating expenses and extend the cash runway to mid-2023.
- The company believes these decisions allow Trevena to continue to sufficiently resource its key strategic priorities of driving commercial adoption of Olinvyk and developing TRV045.
- TRV045 is being developed for acute and chronic neuropathic pain secondary to diabetic peripheral neuropathy.
- Trevena ended the June quarter with approximately $49.5 million in cash.
- Price Action: TRVN shares are up 8.61% at $0.29 during the market session on the last check Thursday.
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