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NCT00955292 · ClinicalTrials.gov registry record · Phase 1
Dose-escalation Study of Quarfloxin in Patients With Advanced Solid Tumors or Lymphomas
A Phase 1 study, sponsored by Cylene Pharmaceuticals.
- Terminated
- Registry status
- Phase 1
- Development phase
- 12
- Enrollment target
NCT00955292: Clinical Trial Phase 1 study, sponsored by Cylene Pharmaceuticals.
NCT00955292 is a Phase 1 study that was terminated before completion, run by Cylene Pharmaceuticals. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00955292, a Phase 1 study, was terminated before completion, sponsored by Cylene Pharmaceuticals.
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 12 participants
- Enrollment target
Study Summary
This phase 1 study of quarfloxin (CX-3543) is designed to test the safety, tolerability, and highest safe dose of this drug when administered intravenously weekly for three weeks of a four week cycle in patients with advanced solid tumors.
Interventions
- DRUG Quarfloxin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2007-07 |
| Est. Completion | 2008-12 |
| Phase | Phase 1 |
Why NCT00955292 stopped before completion
NCT00955292 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).
The record links to 0 conditions, and to 1 intervention - of which Quarfloxin is the first listed.
NCT00955292 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00955292 about?
NCT00955292 is a clinical study titled "Dose-escalation Study of Quarfloxin in Patients With Advanced Solid Tumors or Lymphomas". This phase 1 study of quarfloxin (CX-3543) is designed to test the safety, tolerability, and highest safe dose of this drug when administered intravenously weekly for three weeks of a four week cycle in patients with advanced solid tumors.
What is the current status of trial NCT00955292?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2007-07. Estimated completion is 2008-12.
What interventions are being tested in trial NCT00955292?
The interventions under investigation include: Quarfloxin (DRUG).
Who is sponsoring clinical trial NCT00955292?
This trial is sponsored by Cylene Pharmaceuticals, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00955292's enrollment target sits among peer trials
12 1852nd of 2000 higher than 90 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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