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Terminated Phase 1 Interventional

Dose-escalation Study of Quarfloxin in Patients With Advanced Solid Tumors or Lymphomas

ClinicalTrials.gov ID: NCT00955292

Public ClinicalTrials.gov record NCT00955292. 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 May 8, 2026, 8:08 AM 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 I, Multicenter, Open-label, Dose-Escalation, Safety, Pharmacokinetic and Pharmacodynamic Study of Quarfloxin Administered Intravenously Weekly for Three Weeks of a Four Week Cycle in Patients With Advanced Solid Tumors or Lymphomas

Study identification

NCT ID
NCT00955292
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Cylene Pharmaceuticals
Industry
Enrollment
12 participants

Conditions and interventions

Interventions

  • Quarfloxin Drug

Drug

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
Jun 30, 2007
Primary completion
Mar 31, 2008
Completion
Nov 30, 2008
Last update posted
Aug 9, 2009

2007 – 2008

United States locations

U.S. sites
2
U.S. states
2
U.S. cities
2
Facility City State ZIP Site status
Not listed Scottsdale Arizona
Not listed San Antonio Texas

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 NCT00955292, 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 Aug 9, 2009 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00955292 live on ClinicalTrials.gov.

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