Bioequivalence Between WE 941 OD and Brotizolam (Lendormin®) in Healthy Adult Males
NCT02218658 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2014-08-18
Summary
The bioequivalence of WE 941 OD tablets prepared in oral disintegrating tablet form taken without water and brotizolam conventional tablets (Lendormin® tablets) taken with water, was evaluated in healthy adult male subjects (open-labelled, 2-way cross-over study)
Conditions
- Healthy
Interventions
- DRUG
-
WE941 OD tablets
- DRUG
-
Brotizolam
Sponsors & Collaborators
- lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 20 Years
- Max Age
- 35 Years
- Sex
- MALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2000-07-31
- Primary Completion
- 2000-08-31
More Related Trials
-
Bioequivalence Study Comparing Two Formulations of Escitalopram
NCT01395433 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Two Octreotide Microsphere Formulations in Healthy Volunteers
NCT06254235 ·Status: COMPLETED ·Phase: PHASE1
-
To Test Bioequivalence Between Two Tablet Formulations in the Treatment of Allergy
NCT01322282 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Of A Test Alprazolam Sublingual Formulation Compared To A Commercial Sublingual Formulation
NCT00877955 ·Status: WITHDRAWN ·Phase: PHASE1
-
Relative Bioavailability of 2 Oral Formulations of Nintedanib
NCT02572752 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence of the New Formulation of WAL 801 CL Dry Syrup Compared to the Conventional Formulation of WAL 801 CL Dry Syrup in Healthy Male Volunteers
NCT02260050 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence of Alprazolam Sublingual vs Oral Tablets
NCT00860119 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Dose in Healthy Subjects Under Fed Conditions
NCT01190761 ·Status: COMPLETED ·Phase: PHASE1
-
A Bioequivalence Study of CT-L02 Compared to Co-administration (CTL0201 and CTL0202) in Healthy Volunteers
NCT07128654 ·Status: COMPLETED ·Phase: PHASE1
-
The Bioequivalence Study of Lamotrigine Dispersible/Chewable Tablets 100mg Compared With Compressed Tablet 100 mg
NCT02064465 ·Status: COMPLETED ·Phase: PHASE1
-
Fasting Study of Levothyroxine Sodium Tablets 300 μg to Levothroid® Tablets 300 μg
NCT00648700 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Escitalopram Tablets 10 mg
NCT01745601 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Bosentan 125 mg Tablets Immediate Release (IR) Versus Tracleer® 125 mg Tablets IR In Healthy Subjects
NCT04101370 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence of a New and a Commercial Alprazolam Sublingual Formulation
NCT01285505 ·Status: WITHDRAWN ·Phase: PHASE1
-
Bioequivalence Study of Clonazepam 2 Mg Tablets
NCT06834503 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
A Study to Demonstrate the Bioequivalence of Lacosamide Tablets and Dry Syrup in Healthy Male Japanese Subjects
NCT02972125 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Torrent Pharmaceutical Ltd.'s Olanzapine Orally Disintegrating 5mg Tablets Under Fed Condition
NCT01996501 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate the Bioequivalence of Lacosamide Tablet (200mg) and Syrup (10mg/ml) in Healthy Chinese Male Subjects
NCT03086382 ·Status: COMPLETED ·Phase: PHASE1
-
A Bioequivalence Study Of 4 Mg Fesoterodine Extended-Release Tablets (Toviaz™) In Healthy Subjects
NCT00902187 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Test of "Dong-a Bepotastine Besilate Tab" and "Twolion Tab"
NCT03932435 ·Status: COMPLETED ·Phase: NA
-
A Bioequivalence Study Of A New Alprazolam Dropped Formulation Versus Alprazolam Tablets
NCT01322867 ·Status: COMPLETED ·Phase: PHASE4
-
Fasting Study of Levothyroxine Sodium Tablets 300 μg to Synthroid® Tablets 300 μg
NCT00647855 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Brexpiprazole Orally Disintegrating Tablets (ODT) 2mg
NCT03902574 ·Status: COMPLETED ·Phase: PHASE1
-
Trial to Evaluate Bioequivalence of LCB01-0371 in Different Batches
NCT04939779 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Sotalol, Tablets, 160 mg (Pharmtechnology LLC, Belarus), and Sotalex ®, Tablets, 160 mg (Bristol-Myers Squibb GmbH & Co. KGaA, Germany), in Healthy Volunteers Under Fasting Conditions
NCT03799536 ·Status: COMPLETED ·Phase: PHASE1