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Completed Phase 2 Interventional

Quarfloxin in Patients With Low to Intermediate Grade Neuroendocrine Carcinoma

ClinicalTrials.gov ID: NCT00780663

Public ClinicalTrials.gov record NCT00780663. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 6:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multi-Center, Open Label Study Evaluating the Efficacy and Safety of Quarfloxin in Patients With Low to Intermediate Grade Neuroendocrine Carcinoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 2, open-label, multicenter, efficacy and safety study of quarfloxin in patients with low or intermediate grade neuroendocrine cancer. The purpose of this study is to evaluate the rate of clinical benefit response to quarfloxin treatment including the reduction in secretory symptoms of flushing and/or diarrhea or the reduction quantifiable hormones or other biochemical tumor markers.

Study identification

NCT ID
NCT00780663
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cylene Pharmaceuticals
Industry
Enrollment
25 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2008 (Type not available)
Primary completion
Mar 2010 (Actual)
Completion
Mar 2010 (Actual)
Last update posted
Jun 15, 2011

2008 – 2010

United States locations

U.S. sites
13
U.S. states
6
U.S. cities
13
Facility City State ZIP Site status
Birmingham Hematology and Oncology Birmingham Alabama — —
Rocky Mountain Cancer Centers Denver Colorado 80218 —
Front Range Cancer Specialists Fort Collins Colorado — —
Not listed Ocala Florida 34471 —
Southern New Mexico Cancer Center Las Cruces New Mexico — —
Texas Oncology Amarillo Texas — —
Texas Oncology Dallas Texas 75246 —
El Paso Cancer Treatment Center El Paso Texas — —
Cancer Care Centers of South Texas Kerrville Texas — —
UT Health Science Center San Antonio Texas 78229 —
Tyler Cancer Center Tyler Texas 75702 —
Virginia Mason Medical Center Seattle Washington 98101 —
Northwest Cancer Specialists Vancouver Washington 98684 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00780663, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 15, 2011 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00780663 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →