WHO ICTRP trial

Bioequivalence study of Diosmin 450 mg + Hesperidin 50 mg film-coated tablet in…

CTRI/2025/02/080636 · Clinical Trials Registry India (CTRI) · Not Recruiting

Key facts

Trial ID CTRI/2025/02/080636
Public title Bioequivalence study of Diosmin 450 mg + Hesperidin 50 mg film-coated tablet in healthy, adult human, subjects under fed conditions.
Scientific title An Open label, balanced, randomized, truncated, two treatment, two-period, two-sequence, single dose, crossover, oral bioequivalence study of Pilestop Tablet (Diosmin 450 mg + Hesperidin 50 mg film-coated tablet) by The ACME Laboratories Ltd., with Daflon 500 Tablet (Diosmin 450 mg + Hesperidin 50…
Primary sponsor The ACME Laboratories Ltd.,
Registry Clinical Trials Registry India (CTRI)
Recruitment status Not Recruiting
Study type BA/BE
Countries India
Interventions Intervention1: Pilestop Tablet (Diosmin 450 mg + Hesperidin 50 mg film-coated tablet): Name of the drug: Pilestop Tablet (Diosmin 450 mg + Hesperidin 50 mg film-coated tablet), Route of administration: Oral, Frequency: single oral dose…
Registration date Feb 17, 2025
Target size 24
Secondary IDs ICBio/013/0424, Version: 00, Dated: 29 Apr 2024
Registry page ctri.nic.in

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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