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NCT02522208 · ClinicalTrials.gov registry record · Phase 1

Pharmacodynamic and Pharmacokinetic Study of BiDil Extended-release Capsules and Commercial BiDil Tablets

A Phase 1 study, sponsored by Arbor Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
12
Enrollment target

NCT02522208: Completed Phase 1 study, sponsored by Arbor Pharmaceuticals.

NCT02522208 is a Phase 1 study that has completed, run by Arbor Pharmaceuticals. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02522208, a Phase 1 study, has completed, sponsored by Arbor Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
12 participants
Enrollment target

Study Summary

This study will investigate cardiovascular parameters using echocardiographic and pharmacokinetics during a daily dose of BiDil and BiDil Extended Release (XR) compared to a study drug free day.

Primary Outcome

assess the treatment effect of BiDil and BiDil XR on Pulmonary Artery Systolic Pressure (PASP) by Doppler echocardiography

Interventions

  • DRUG BiDil XR
  • DRUG BiDil Immediate Release (IR)

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2015-09
Est. Completion 2016-04
Phase Phase 1
Arbor Pharmaceuticals

14 total trials

What the finished NCT02522208 record still lists

NCT02522208 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).

The record links to 0 conditions, and to 2 interventions - of which BiDil XR is the first listed.

NCT02522208 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02522208 about?

NCT02522208 is a clinical study titled "Pharmacodynamic and Pharmacokinetic Study of BiDil Extended-release Capsules and Commercial BiDil Tablets". This study will investigate cardiovascular parameters using echocardiographic and pharmacokinetics during a daily dose of BiDil and BiDil Extended Release (XR) compared to a study drug free day.

What is the current status of trial NCT02522208?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2015-09. Estimated completion is 2016-04.

What interventions are being tested in trial NCT02522208?

The interventions under investigation include: BiDil XR (DRUG), BiDil Immediate Release (IR) (DRUG).

Who is sponsoring clinical trial NCT02522208?

This trial is sponsored by Arbor Pharmaceuticals, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02522208's enrollment target sits among peer trials

12 1852nd of 2000 higher than 90 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 NCT02522208, the US trial registry maintained by the National Library of Medicine. NCT02522208 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.