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NCT01313065 · ClinicalTrials.gov registry record · Phase 1
Evaluation of Safety, Tolerability, PK & PD of Intravenous VX15/2503 in Patients With Advanced Solid Tumors
A Phase 1 study, sponsored by Vaccinex.
- Completed
- Registry status
- Phase 1
- Development phase
- 42
- Enrollment target
NCT01313065: Completed Phase 1 study, sponsored by Vaccinex.
NCT01313065 is a Phase 1 study that has completed, run by Vaccinex. The registered enrollment target is 42 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01313065, a Phase 1 study, has completed, sponsored by Vaccinex.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 42 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety and tolerability of IV administration of VX15/2503 in patients with advanced solid tumors. The escalation part of the study will determine the maximum tolerated dose (MTD).
Primary Outcome
Subject incidence of treatment-emergent adverse events
Interventions
- DRUG VX15/2503
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 42 participants |
| Start Date | 2011-01 |
| Est. Completion | 2014-06 |
| Phase | Phase 1 |
What the finished NCT01313065 record still lists
NCT01313065 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (30% lower).
The record links to 0 conditions, and to 1 intervention - of which VX15/2503 is the first listed.
NCT01313065 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01313065 about?
NCT01313065 is a clinical study titled "Evaluation of Safety, Tolerability, PK & PD of Intravenous VX15/2503 in Patients With Advanced Solid Tumors". The purpose of this study is to evaluate the safety and tolerability of IV administration of VX15/2503 in patients with advanced solid tumors. The escalation part of the study will determine the maximum tolerated dose (MTD).
What is the current status of trial NCT01313065?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 42 participants. The study started on 2011-01. Estimated completion is 2014-06.
What interventions are being tested in trial NCT01313065?
The interventions under investigation include: VX15/2503 (DRUG).
Who is sponsoring clinical trial NCT01313065?
This trial is sponsored by Vaccinex, which has 7 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01313065's enrollment target sits among peer trials
42 1105th of 2000 higher than 876 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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