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NCT01159730

A Phase II, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Assess the Effect of Multiple Doses of VB-201 on Biomarkers

Completed Phase 2 Last updated 15 November 2011
What this trial tests

Phase 2 trial testing VB-201 or Placebo in Biomarker in 320 participants. Completed in 1 October 2011.

Timeline
1 October 2010
Primary endpoint
1 October 2011
1 October 2011

Quick facts

Lead sponsorVascular Biogenics Ltd. operating as VBL Therapeutics
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Enrollment320
Start date1 October 2010
Primary completion1 October 2011
Estimated completion1 October 2011
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Vascular Biogenics Ltd. operating as VBL Therapeutics — full company profile →

Who can join

Adults 18 to 75, any sex, with Biomarker. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to assess the safety and tolerability of multiple doses of VB-201 administered for 4 weeks and its efficacy on biomarkers.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Biomarker

Currently open trials in the same condition.

Other Vascular Biogenics Ltd. operating as VBL Therapeutics trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01159730.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing