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NCT01106508 · ClinicalTrials.gov registry record · Phase 1
A Dose Finding and Safety Study of Oral LEQ506 in Patients With Advanced Solid Tumors
A Phase 1 study, sponsored by Novartis Pharmaceuticals.
- Completed
- Registry status
- Phase 1
- Development phase
- 57
- Enrollment target
NCT01106508: Completed Phase 1 study, sponsored by Novartis Pharmaceuticals.
NCT01106508 is a Phase 1 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 57 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01106508, a Phase 1 study, has completed, sponsored by Novartis Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 57 participants
- Enrollment target
Study Summary
This first-in-human dose-escalation study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics of LEQ506 given orally on a daily dosing schedule in patients with advanced solid tumors.
Interventions
- DRUG LEQ506
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 57 participants |
| Start Date | 2010-10 |
| Est. Completion | 2015-06 |
| Phase | Phase 1 |
What the finished NCT01106508 record still lists
NCT01106508 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 57 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 1 intervention - of which LEQ506 is the first listed.
NCT01106508 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01106508 about?
NCT01106508 is a clinical study titled "A Dose Finding and Safety Study of Oral LEQ506 in Patients With Advanced Solid Tumors". This first-in-human dose-escalation study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics of LEQ506 given orally on a daily dosing schedule in patients with advanced solid tumors.
What is the current status of trial NCT01106508?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 57 participants. The study started on 2010-10. Estimated completion is 2015-06.
What interventions are being tested in trial NCT01106508?
The interventions under investigation include: LEQ506 (DRUG).
Who is sponsoring clinical trial NCT01106508?
This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01106508's enrollment target sits among peer trials
57 901st of 2000 higher than 1,099 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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