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NCT02078648 · ClinicalTrials.gov registry record · Phase 1

Safety and Efficacy Study of SL-701, a Glioma-Associated Antigen Vaccine To Treat Recurrent Glioblastoma Multiforme

A Phase 1 study, sponsored by Stemline Therapeutics.

Completed
Registry status
Phase 1
Development phase
74
Enrollment target

NCT02078648: Completed Phase 1 study, sponsored by Stemline Therapeutics.

NCT02078648 is a Phase 1 study that has completed, run by Stemline Therapeutics. The registered enrollment target is 74 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02078648, a Phase 1 study, has completed, sponsored by Stemline Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
74 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety and efficacy of SL-701 as a treatment for recurrent glioblastoma multiform (GBM).

Primary Outcome

RLT included any events that occurred anytime through the first 12 doses of study treatment that were considered possibly, probably, or definitely related to investigational therapy and ranged from Grade ≥3 bronchospasm or Grade 2 bronchospasm that did not resolve within 24 hours despite appropriate medical treatment to cerebral edema associated with severe clinical manifestations (Grade 4) that were considered related to study therapy by the investigator.

Interventions

  • DRUG Bevacizumab
  • DRUG Imiquimod
  • DRUG SL-701; poly-ICLC (polyinosinic-polycytidylic acid stabilized with polylysine and carboxymethyl cellulose)
  • DRUG SL-701 + GM-CSF

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2014-05
Est. Completion 2018-01-22
Phase Phase 1
Stemline Therapeutics

17 total trials

What the finished NCT02078648 record still lists

NCT02078648 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% higher).

The record links to 0 conditions, and to 4 interventions - of which Bevacizumab is the first listed.

NCT02078648 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02078648 about?

NCT02078648 is a clinical study titled "Safety and Efficacy Study of SL-701, a Glioma-Associated Antigen Vaccine To Treat Recurrent Glioblastoma Multiforme". The purpose of this study is to determine the safety and efficacy of SL-701 as a treatment for recurrent glioblastoma multiform (GBM).

What is the current status of trial NCT02078648?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 74 participants. The study started on 2014-05. Estimated completion is 2018-01-22.

What interventions are being tested in trial NCT02078648?

The interventions under investigation include: Bevacizumab (DRUG), Imiquimod (DRUG), SL-701; poly-ICLC (polyinosinic-polycytidylic acid stabilized with polylysine and carboxymethyl cellulose) (DRUG), SL-701 + GM-CSF (DRUG).

Who is sponsoring clinical trial NCT02078648?

This trial is sponsored by Stemline Therapeutics, which has 17 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02078648's enrollment target sits among peer trials

74 725th of 2000 higher than 1,269 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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Source: ClinicalTrials.gov NCT02078648, the US trial registry maintained by the National Library of Medicine. NCT02078648 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.