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NCT01506791 · ClinicalTrials.gov registry record · Phase 1

Bioequivalence Study of Desloratadine and Pseudoephedrine Extended-release Tablets Under Fed Conditions

A Phase 1 study, sponsored by Dr. Reddy's Laboratories Limited.

Completed
Registry status
Phase 1
Development phase
44
Enrollment target

NCT01506791: Completed Phase 1 study, sponsored by Dr. Reddy's Laboratories Limited.

NCT01506791 is a Phase 1 study that has completed, run by Dr. Reddy's Laboratories Limited. The registered enrollment target is 44 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01506791, a Phase 1 study, has completed, sponsored by Dr. Reddy's Laboratories Limited.

COMPLETED
Registry status
Phase 1
Development phase
44 participants
Enrollment target

Study Summary

This is an open label, randomised, 2-way crossover, comparative bioequivalence study.

Interventions

  • DRUG Desloratadine and pseudoephedrine

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2006-04
Est. Completion 2006-04
Phase Phase 1
Dr. Reddy's Laboratories Limited

52 total trials

What the finished NCT01506791 record still lists

NCT01506791 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower).

The record links to 0 conditions, and to 1 intervention - of which Desloratadine and pseudoephedrine is the first listed.

NCT01506791 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01506791 about?

NCT01506791 is a clinical study titled "Bioequivalence Study of Desloratadine and Pseudoephedrine Extended-release Tablets Under Fed Conditions". This is an open label, randomised, 2-way crossover, comparative bioequivalence study.

What is the current status of trial NCT01506791?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2006-04. Estimated completion is 2006-04.

What interventions are being tested in trial NCT01506791?

The interventions under investigation include: Desloratadine and pseudoephedrine (DRUG).

Who is sponsoring clinical trial NCT01506791?

This trial is sponsored by Dr. Reddy's Laboratories Limited, which has 52 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01506791's enrollment target sits among peer trials

44 1086th of 2000 higher than 901 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01506791, the US trial registry maintained by the National Library of Medicine. NCT01506791 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.