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NCT00958841 · ClinicalTrials.gov registry record · Phase 2

Study of Pasireotide in Patients With Rare Tumors of Neuroendocrine Origin

A Phase 2 study, sponsored by Novartis Pharmaceuticals.

Terminated
Registry status
Phase 2
Development phase
118
Enrollment target

NCT00958841: Clinical Trial Phase 2 study, sponsored by Novartis Pharmaceuticals.

NCT00958841 is a Phase 2 study that was terminated before completion, run by Novartis Pharmaceuticals. The registered enrollment target is 118 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (11% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00958841, a Phase 2 study, was terminated before completion, sponsored by Novartis Pharmaceuticals.

TERMINATED
Registry status
Phase 2
Development phase
118 participants
Enrollment target

Study Summary

This study will assess the effectiveness and safety of pasireotide long-acting release in patients who have rare tumors of neuroendocrine origin.

Primary Outcome

The primary efficacy endpoint was defined as the percentage of responders at Month 6 among pooled PNET patients (insulinoma, gastrinoma, VIPoma, and glucagonoma). A responder was defined as a patient who either attained normalization or had a greater than 50% reduction from baseline of the level of the primary biochemical tumor marker at Month 6 (M6). Four insulinoma pts were excluded from analysis because of unavailability of normal ranges for the associated primary biochemical tumor marker (in

Interventions

  • DRUG pasireotide LAR

Trial Details

FieldValue
Enrollment Target 118 participants
Start Date 2009-09
Est. Completion 2015-06
Phase Phase 2
Novartis Pharmaceuticals

1,375 total trials

Why NCT00958841 stopped before completion

NCT00958841 is an interventional study that assigns participants to a tested intervention. The registered 118 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (11% lower).

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

NCT00958841 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00958841 about?

NCT00958841 is a clinical study titled "Study of Pasireotide in Patients With Rare Tumors of Neuroendocrine Origin". This study will assess the effectiveness and safety of pasireotide long-acting release in patients who have rare tumors of neuroendocrine origin.

What is the current status of trial NCT00958841?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 118 participants. The study started on 2009-09. Estimated completion is 2015-06.

What interventions are being tested in trial NCT00958841?

The interventions under investigation include: pasireotide LAR (DRUG).

Who is sponsoring clinical trial NCT00958841?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00958841's enrollment target sits among peer trials

118 618th of 2000 higher than 1,378 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00958841, the US trial registry maintained by the National Library of Medicine. NCT00958841 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.