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NCT00050635 · ClinicalTrials.gov registry record · Phase 4

STOP Trial - Sandostatin LAR Depot Trial for the Optimum Prevention of Chemotherapy Induced Diarrhea

A Phase 4 study, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 4
Development phase
150
Enrollment target

NCT00050635 is a Phase 4 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 150 participants.

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The verdict

NCT00050635, a Phase 4 study, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 4
Development phase
150 participants
Enrollment target

Study Summary

Currently there is an ongoing clinical trial for patients with chemotherapy induced diarrhea. This trial is being conducted to evaluate the efficacy of two dose levels (30 mg and 40 mg) of an investigational drug in reducing the occurrence of severe (Grade 3 or 4) diarrhea during chemotherapy. Eligible patients must either have experienced NCI Common Toxicity Grade 1 - 4 chemotherapy-induced diarrhea during previous chemotherapy treatment or be experiencing Grade 1-4 chemotherapy-induced diarrhea currently. In order to participate in this clinical trial, patients must be male or female 18 years of age or older. Inclusion into this investigational drug trial is based on the protocol entry criteria and a detailed evaluation from a participating trial investigator

Interventions

  • DRUG Sandostatin LAR Depot

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2002-12
Est. Completion 2003-07
Phase Phase 4

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT00050635

The ClinicalTrials.gov registry entry for NCT00050635 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

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

NCT00050635 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00050635 about?

NCT00050635 is a clinical study titled "STOP Trial - Sandostatin LAR Depot Trial for the Optimum Prevention of Chemotherapy Induced Diarrhea". Currently there is an ongoing clinical trial for patients with chemotherapy induced diarrhea. This trial is being conducted to evaluate the efficacy of two dose levels (30 mg and 40 mg) of an investigational drug in reducing the occurrence of severe (Grade 3 or 4) diarrhea during chemotherapy. Eligi...

What is the current status of trial NCT00050635?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 150 participants. The study started on 2002-12. Estimated completion is 2003-07.

What interventions are being tested in trial NCT00050635?

The interventions under investigation include: Sandostatin LAR Depot (DRUG).

Who is sponsoring clinical trial NCT00050635?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.