Found 13 matching trials
Comparative Bioequivalence Study in Adult Patients Suffering From Chronic Myeloid Leukemia & Gastrointestinal Stromal Tumor Under Fed Conditions PHASE2 To characterize pharmacokinetic profile of test product compared to that of...
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Kailash Cancer Hospital & Research Centre
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Long Acting Buprenorphine Injection Compared to Sublingual Buprenorphine/Naloxone Films PHASE2 While substance use disorders have been found to have relapse rates on part...
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Multiple Locations
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Monthly Versus Daily Buprenorphine Formulations for Treatment of Opiate Use Disorder PHASE4 Opioid use disorder and opioid-related deaths are increasing across Canada....
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Royal Victoria Regional Health Centre
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Treatment Seeking Participants With Opioid Use Disorders Assessing Tolerability of Depot Injections of Buprenorphine PHASE3 This is a randomized, double-blind, placebo controlled, multicenter study i...
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Haleyville Clinical Research
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A Comparative Bioavailability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tamsulosin 0.4 mg Tablets, in Healthy Adult Male Subjects, Under Fed Conditions PHASE1 The aim of this study is to evaluate the bioequivalence and safety of Tamsu...
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Active Not Recruiting
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Effect of Sublingual Formulation of Dexmedetomidine HCl (BXCL501) - Alcohol Interaction Study PHASE1 The overall objective of the proposed study is to determine if Dexmedetomid...
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VA Connecticut Healthcare System
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SL-START - SubLingual Apomorphine Schemes of TitrAtion in Real-world Treatment N/A The purpose of the study is to generate real-world evidence data for the on...
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Charité - Universitätsmedizin Berlin - Sektion für Bewegungsstörungen und Neuromodulation
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ACTIV-2: A Study for Outpatients With COVID-19 PHASE2 Drug studies often look at the effect one or two drugs have on a medical co...
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Pinnacle Research Group (Site 1082), 321 E. 10th Street
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A Comparative Bioavalability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tabsulosine 0.4 mg Tablets in Healthy Adult Male Subjects, at Steady State PHASE1 The aim of this study is to evaluate the bioequivalence and safety of Tamsu...
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Active Not Recruiting
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Effect of Sublingual Formulation of Dexmedetomidine Hydrochloride (HCl) (BXCL501) - Outpatient Study PHASE1 The overall objective of the proposed study is to determine if Dexmedetomid...
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VA Connecticut Healthcare System
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