Bioequivalency Study of Montelukast 10 mg Tablets Under Fasted Conditions
NCT01659931 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 34
Last updated 2018-01-23
Summary
The objective of this study was to prove the bioequivalence of Montelukast Tablet under fasted conditions
Conditions
Interventions
- DRUG
-
Montelukast
10 mg Tablet
- DRUG
-
Singulair
10 mg Tablet
Sponsors & Collaborators
-
Roxane Laboratories
lead INDUSTRY
Principal Investigators
-
Alan K Copa, PharmD · PRACS Institute, Ltd.
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2008-02-29
- Primary Completion
- 2008-02-29
- Completion
- 2008-02-29
Countries
- United States
Study Locations
More Related Trials
-
Bioequivalence of GW483100 10 Milligram (mg) Tablets in Healthy Subjects Under Fasting Conditions
NCT02658422 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Torrent Pharmaceutical Ltd.'s Montelukast Sodium 10mg Tablet Under Fed Conditions
NCT01928069 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Montelukast Sodium Oral Granules 4mg Under Fed Condition
NCT01691469 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Montelukast Sodium Oral Thin Film and Chewable Tablet in Fasted Healthy Volunteers
NCT05528198 ·Status: COMPLETED ·Phase: NA
-
Bioequivalence Study of Montelukast Sodium Chewable Tablets 4mg and 5mg Under Fed Condition
NCT01674517 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Montelukast Sodium Chewable Tablets 4mg and 5mg Under Fasting Condition
NCT01674504 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Montelukast Sodium Tablets 10mg Under Fed Condition
NCT01671722 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Bioavailability Study of Two Montelukast Sodium (GW483100) 5 Milligrams (mg) Chewable Tablets and One Reference Montelukast Sodium 5 mg Chewable Tablet in Healthy Adult Subjects
NCT02322671 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalency Study of Meloxicam Tablets Under Fasting Conditions
NCT00618163 ·Status: COMPLETED ·Phase: NA
-
Bioequivalence Study for Desloratadine OD Tablets 5 mg Under Fasting Condition
NCT01506050 ·Status: COMPLETED ·Phase: PHASE1
-
Bio Equivalence Study of Torrent Pharmaceutical Ltd's Rosuvastatin Calcium Tablets Under Fasting Condition.
NCT02962310 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Desloratadine and Pseudoephedrine Sulfate Extended-release Tablets Under Fasting Conditions
NCT01373138 ·Status: COMPLETED ·Phase: PHASE1
-
A Relative Bioavailability Study of Ramipril 10 mg Capsules Under Fed Conditions
NCT00864162 ·Status: COMPLETED ·Phase: PHASE1
-
Ramipril 10 mg Capsule in Healthy Subjects Under Fasting Conditions
NCT00828321 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalency Study of Amlodipine Tablets Under Fasting Conditions
NCT00602017 ·Status: COMPLETED ·Phase: NA
-
A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Fasting Conditions
NCT00864279 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Bilastine Tablets in Healthy Chinese Subjects
NCT06098261 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1
-
Bioequivalence Study on Loratadine Orally Disintegrating Tablets 10 mg Under Fasting Conditions
NCT00776217 ·Status: COMPLETED ·Phase: NA
-
A Study to Assess the Bioequivalence of Xisimin (Loratadine) Tablets Under Fasting and Fed Conditions in Healthy Participants Compared With Clarityne Tablets
NCT03196531 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalence Study of Cetirizine Hydrochloride 10mg Tablets Under Fasting Conditions
NCT00776139 ·Status: COMPLETED ·Phase: NA
-
Bioequivalency Study of Losartan Potassium 100 mg Tablet Under Fasted Conditions
NCT01216852 ·Status: COMPLETED ·Phase: NA
-
Anastrozole 1 mg Tablets Under Fasting Conditions
NCT01182181 ·Status: COMPLETED ·Phase: PHASE1
-
Bioequivalency Study of Ramipril 10 mg Capsules Under Fasting Conditions
NCT00702091 ·Status: COMPLETED ·Phase: NA
-
A Relative Bioavailability Study of Ramipril 10 mg Capsules Under Fasting Conditions
NCT00864448 ·Status: COMPLETED ·Phase: PHASE1
-
A Manufacturing Transfer Study Comparing the Bioequivalence of a Single Oral Dose of Claritin-D 12-Hour Extended Release Tablet From 2 Different Manufacturers Under Fasted Conditions in Healthy Adult Subjects
NCT03517930 ·Status: COMPLETED ·Phase: PHASE1