CLINICAL TRIALS PROFILE FOR SB-649868
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Clinical Trials for SB-649868
| Trial ID | Title | Status | Sponsor | Phase | Summary |
|---|---|---|---|---|---|
| NCT00426816 ↗ | To Evaluate The Effects Of SB-649868 (10, 30 Mg And 60 Mg) On Subjects With Primary Insomnia | Completed | GlaxoSmithKline | Phase 2 | This study to evaluate the effects of SB-649868 (10, 30 mg and 60 mg) on sleep continuity, PSG sleep recordings, subjective sleep assessment, and daytime cognitive function in subjects with primary insomnia |
| NCT00440323 ↗ | Disturbed Sleep Model Study. | Completed | GlaxoSmithKline | Phase 1 | Subjects will be screened within 28 days. Each treatment session will consist of 2 PSG nights, study drug administration and noise model is conducted on second night. |
| NCT00495274 ↗ | Bioequivalence and Food Effect Study in Healthy Volunteers | Completed | GlaxoSmithKline | Phase 1 | The purpose of this study is to select the formulation with the optimal pharmacokinetic profile for an hypnotic drug to further develop in the market. |
| NCT00495729 ↗ | 15-Day Repeated-Dose Study With SB-649868 And Its Interaction With CYP3A4 Isoenzyme In Healthy Male Subjects. | Completed | GlaxoSmithKline | Phase 1 | Subjects will be screened within 28 days, Simvastatin dose and single SB-649868 dose 10 and 7 days prior to repeat dosing respectively, 15 days SB-649868 repeat dosing with safety and cognition function tests. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Summary |
Clinical Trial Conditions for SB-649868
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Clinical Trial Locations for SB-649868
Clinical Trial Progress for SB-649868
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Clinical Trial Sponsors for SB-649868
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