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NCT01794793 · ClinicalTrials.gov registry record · Phase 4

Study to Allow Access to Pasireotide for Patients Benefiting From Pasireotide Treatment in Novartis-sponsored Studies

A Phase 4 study, sponsored by Recordati Group.

Completed
Registry status
Phase 4
Development phase
337
Enrollment target

NCT01794793: Completed Phase 4 study, sponsored by Recordati Group.

NCT01794793 is a Phase 4 study that has completed, run by Recordati Group. The registered enrollment target is 337 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01794793, a Phase 4 study, has completed, sponsored by Recordati Group.

COMPLETED
Registry status
Phase 4
Development phase
337 participants
Enrollment target

Study Summary

The purpose of this study is to allow continued use of pasireotide in patients who are on pasireotide treatment in a Novartis-sponsored study and are benefiting from the treatment as judged by the investigator.

Primary Outcome

Collect long term safety data, i.e. SAEs and AEs. SAES will be reviewed and reported as part of the regular pharmacovigilance activities.

Interventions

  • DRUG Cabergoline
  • DRUG Pasireotide
  • DRUG Pasireotide LAR

Trial Details

FieldValue
Enrollment Target 337 participants
Start Date 2013-06-10
Est. Completion 2023-07-25
Phase Phase 4
Recordati Group

11 total trials

What the finished NCT01794793 record still lists

NCT01794793 is an interventional study that assigns participants to a tested intervention. The registered 337 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (35% lower).

The record links to 0 conditions, and to 3 interventions - of which Cabergoline is the first listed.

NCT01794793 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01794793 about?

NCT01794793 is a clinical study titled "Study to Allow Access to Pasireotide for Patients Benefiting From Pasireotide Treatment in Novartis-sponsored Studies". The purpose of this study is to allow continued use of pasireotide in patients who are on pasireotide treatment in a Novartis-sponsored study and are benefiting from the treatment as judged by the investigator.

What is the current status of trial NCT01794793?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 337 participants. The study started on 2013-06-10. Estimated completion is 2023-07-25.

What interventions are being tested in trial NCT01794793?

The interventions under investigation include: Cabergoline (DRUG), Pasireotide (DRUG), Pasireotide LAR (DRUG).

Who is sponsoring clinical trial NCT01794793?

This trial is sponsored by Recordati Group, which has 11 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01794793's enrollment target sits among peer trials

337 250th of 2000 higher than 1,751 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT01794793, the US trial registry maintained by the National Library of Medicine. NCT01794793 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.