Eisai and Purdue Report Result of Lemborexant in P-III SUNRISE 2 Study for Insomnia in Adults
Shots:
- The P-III SUNRISE 2 study involves assessing of Lemborexant (5mg-10mg) vs PBO in 949 patients with insomnia disorder- characterized by difficulty in falling asleep/staying asleep aged 18 to 88yrs.
- P-III SUNRISE 2 study results: reductions in sleep onset latency (sSOL) (-21.81- -28.21 vs -11.43 min); improvement in sSE (14.19%- 14.31% vs 9.64%); reduction in subjective wake after sleep onset (sWASO) (-46.75- -41.95 vs -29.28 min); presented at Sleep Research Society’s on 14 Feb- 2019
- Lemborexant is an orexin neurotransmitter targeted for faster falling asleep with longer period of time with its NDA filled with the US FDA for insomnia on 27 Dec-2018 and is evaluated in P-II for sleep-wake rhythm disorder and mild to moderate Alzheimer's dementia
Click here to read the full press release
This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com