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Clinical Research Directory

Browse clinical research sites, groups, and studies.

5 clinical studies listed.

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Bioequivalance

Tundra lists 5 Bioequivalance clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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COMPLETED

NCT07763899

Clinical Study to Determine Bioequivalence Between Two Oral Medications of Sitagliptin/Metformin in Prolonged-release Tablets With 50 mg/1000 mg in Healthy Subjects, Fast Study.

Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x2, two treatments, two periods, two sequences controlled clinical study.

Gender: All

Ages: 18 Years - 55 Years

Updated: 2026-08-14

1 state

Bioequivalance
COMPLETED

NCT07763964

Clinical Study to Determine Bioequivalence Between Two Oral Medications of Sitagliptin/Metformin in Prolonged-release Tablets With 100 mg/1000 mg in Healthy Subjects, Fed Study.

Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x2, two treatments, two periods, two sequences controlled clinical study

Gender: All

Ages: 18 Years - 55 Years

Updated: 2026-08-14

Bioequivalance
COMPLETED

NCT07763951

Clinical Study to Determine Bioequivalence Between Two Oral Medications of Sitagliptin/Metformin in Prolonged-release Tablets With 100 mg/1000 mg in Healthy Subjects, Fast Study.

Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x2, two treatments, two periods, two sequences controlled clinical study

Gender: All

Ages: 18 Years - 55 Years

Updated: 2026-08-14

1 state

Bioequivalance
COMPLETED

NCT07698275

Clinical Study to Determine Bioequivalence of Oral Tamsulosin Products as 0.4 mg Prolonged-release Tablets in Male Subjects Under Fasted Conditions

Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x4, replicated, two treatments, four periods, two sequences controlled clinical study

Gender: MALE

Ages: 18 Years - 55 Years

Updated: 2026-07-13

1 state

Bioequivalance
COMPLETED

NCT07624357

Bioequivalence Study of Vortioxetine in 20 mg Coated Tablets in Healthy Subjects Under Fasting Conditions

Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x2, two treatments, two periods, two sequences controlled clinical study

Gender: All

Ages: 18 Years - 55 Years

Updated: 2026-06-03

1 state

Bioequivalance