CLINICAL TRIALS PROFILE FOR DAYVIGO
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All Clinical Trials for dayvigo
Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
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NCT04555733 ↗ | A Single and Multiple Dose Study of Lemborexant in Healthy Chinese Participants | Completed | Eisai Co., Ltd. | Phase 1 | 2020-10-26 | The primary objective of this study is to assess the pharmacokinetics (PK) of lemborexant and metabolites (M4, M9, and M10) in plasma in healthy Chinese participants following single and multiple oral doses of lemborexant. |
NCT04818086 ↗ | Drug-drug Interaction Study of Lemborexant as an Adjunctive Treatment for Buprenorphine/Naloxone for Opioid Use Disorder | Recruiting | National Institute on Drug Abuse (NIDA) | Phase 1/Phase 2 | 2021-05-03 | The purpose of this research study is to test the safety, tolerability, drug interactions with buprenorphine-naloxone, and effectiveness lemborexant when used to treat Opioid Use Disorder. |
NCT04818086 ↗ | Drug-drug Interaction Study of Lemborexant as an Adjunctive Treatment for Buprenorphine/Naloxone for Opioid Use Disorder | Recruiting | Virginia Commonwealth University | Phase 1/Phase 2 | 2021-05-03 | The purpose of this research study is to test the safety, tolerability, drug interactions with buprenorphine-naloxone, and effectiveness lemborexant when used to treat Opioid Use Disorder. |
NCT04890561 ↗ | A Study to Evaluate Lemborexant in Milk of Healthy Lactating Women | Completed | Eisai Inc. | Phase 1 | 2021-05-17 | The primary purpose of the study is to estimate the cumulative amount of lemborexant excreted in breast milk following a single dose administration of lemborexant 10 milligram (mg) to healthy lactating women and to estimate the relative infant dose (RID) expressed as a percent of the daily maternal dose. |
>Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
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