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NCT00710125 · ClinicalTrials.gov registry record · Phase 1
Safety Study of GPX-150 in Patients With Solid Tumors
A Phase 1 study, sponsored by Gem Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 27
- Enrollment target
NCT00710125: Completed Phase 1 study, sponsored by Gem Pharmaceuticals.
NCT00710125 is a Phase 1 study that has completed, run by Gem Pharmaceuticals. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00710125, a Phase 1 study, has completed, sponsored by Gem Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 27 participants
- Enrollment target
Study Summary
This is a Phase 1 safety and dose escalation study to define the maximum tolerated dose (MTD) and identify the dose limiting toxicities (DLT) following IV administration of GPX-150 once every 3 weeks. Escalating doses starting at the dose of 14 mg/m2 and increasing to the dose of 265 mg/m2 will be administered IV once every 3 weeks for up to 8 cycles of treatment. Patients who have previously received an anthracycline are limited to 4 cycles of treatment.
Interventions
- DRUG GPX-150 for Injection
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 27 participants |
| Start Date | 2008-01 |
| Est. Completion | 2013-10 |
| Phase | Phase 1 |
What the finished NCT00710125 record still lists
NCT00710125 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).
The record links to 0 conditions, and to 1 intervention - of which GPX-150 for Injection is the first listed.
NCT00710125 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00710125 about?
NCT00710125 is a clinical study titled "Safety Study of GPX-150 in Patients With Solid Tumors". This is a Phase 1 safety and dose escalation study to define the maximum tolerated dose (MTD) and identify the dose limiting toxicities (DLT) following IV administration of GPX-150 once every 3 weeks. Escalating doses starting at the dose of 14 mg/m2 and increasing to the dose of 265 mg/m2 will be a...
What is the current status of trial NCT00710125?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2008-01. Estimated completion is 2013-10.
What interventions are being tested in trial NCT00710125?
The interventions under investigation include: GPX-150 for Injection (DRUG).
Who is sponsoring clinical trial NCT00710125?
This trial is sponsored by Gem Pharmaceuticals, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00710125's enrollment target sits among peer trials
27 1463rd of 2000 higher than 519 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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