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NCT00884715 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics, Efficacy and Safety of an Octreotide Implant in Patients With Carcinoid Syndrome

A Phase 1 study, sponsored by Endo USA Inc., a Keenova Therapeutics Company.

Terminated
Registry status
Phase 1
Development phase
10
Enrollment target

NCT00884715: Clinical Trial Phase 1 study, sponsored by Endo USA Inc., a Keenova Therapeutics Company.

NCT00884715 is a Phase 1 study that was terminated before completion, run by Endo USA Inc., a Keenova Therapeutics Company. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00884715, a Phase 1 study, was terminated before completion, sponsored by Endo USA Inc., a Keenova Therapeutics Company.

TERMINATED
Registry status
Phase 1
Development phase
10 participants
Enrollment target

Study Summary

Evaluate the pharmacokinetics, safety and efficacy of an octreotide implant for the treatment of the symptoms of carcinoid syndrome.

Interventions

  • DRUG Octreotide

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2009-07
Est. Completion 2011-12
Phase Phase 1

Why NCT00884715 stopped before completion

NCT00884715 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

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

NCT00884715 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00884715 about?

NCT00884715 is a clinical study titled "Pharmacokinetics, Efficacy and Safety of an Octreotide Implant in Patients With Carcinoid Syndrome". Evaluate the pharmacokinetics, safety and efficacy of an octreotide implant for the treatment of the symptoms of carcinoid syndrome.

What is the current status of trial NCT00884715?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2009-07. Estimated completion is 2011-12.

What interventions are being tested in trial NCT00884715?

The interventions under investigation include: Octreotide (DRUG).

Who is sponsoring clinical trial NCT00884715?

This trial is sponsored by Endo USA Inc., a Keenova Therapeutics Company, which has 61 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00884715's enrollment target sits among peer trials

10 1913th of 2000 higher than 46 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 NCT00884715, the US trial registry maintained by the National Library of Medicine. NCT00884715 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.