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ACTIVE NOT RECRUITING Phase 3

A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET

NCT05050942 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the effectiveness and safety of CAM2029 to octreotide LAR or lanreotide ATG in patients with advanced, well-differentiated GEP-NET. Patients who experience progressive disease in the randomized part of the study may proceed to an open-label extension part with intensified treatment with CAM2029.

Interventions

  • DRUG Octreotide LAR
  • DRUG CAM2029
  • DRUG Lanreotide ATG

Study Locations (20)

Texas

  • Texas Oncology - Austin — Austin
  • Texas Oncology - Dallas — Dallas
  • Texas Oncology - Denton North — Denton
  • The University of Texas - MD Anderson Cancer Center — Houston
  • Texas Oncology - McAllen — McAllen
  • Texas Oncology - San Antonio Northeast — San Antonio

New York

  • Memorial Sloan-Kettering Cancer Center — New York
  • The Mount Sinai Hospital — The Bronx
  • White Plains Hospital - Center for Cancer Care — White Plains

Florida

  • Mayo Clinic Hospital - Florida — Jacksonville
  • Anderson Family Cancer Institute — Jupiter

Arizona

  • Mayo Clinic Cancer Center (MCCC) - Phoenix — Phoenix

California

  • UCLA Ahmanson Biological Imaging Center — Santa Monica

Colorado

  • Rocky Mountain Cancer Centers - Denver - Midtown — Denver

Kentucky

  • University of Kentucky (UK) - Markey Cancer Center — Lexington

Louisiana

  • East Jefferson General Hospital — Metairie

Trial Details

FieldValue
Enrollment Target 332 participants
Start Date 2021-10-22
Est. Completion 2028-07
Phase Phase 3

Sponsor

Camurus AB

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05050942

The ClinicalTrials.gov registry entry for NCT05050942 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 332 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Camurus AB, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Gastro-enteropancreatic Neuroendocrine Tumor appearing as the primary indexed condition, and to 3 interventions — of which Octreotide LAR is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05050942 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Texas, New York, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05050942 about?

NCT05050942 is a clinical study titled "A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET". The purpose of this study is to compare the effectiveness and safety of CAM2029 to octreotide LAR or lanreotide ATG in patients with advanced, well-differentiated GEP-NET. Patients who experience progressive disease in the randomized part of the study may proceed to an open-label extension part with...

What is the current status of trial NCT05050942?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 332 participants. The study started on 2021-10-22. Estimated completion is 2028-07.

What conditions does trial NCT05050942 study?

This clinical trial studies the following conditions: Gastro-enteropancreatic Neuroendocrine Tumor. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05050942?

The interventions under investigation include: Octreotide LAR (DRUG), CAM2029 (DRUG), Lanreotide ATG (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05050942?

This trial is sponsored by Camurus AB, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05050942 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial