Safety Study on AdCD40L Gene Therapy for Bladder Cancer

NCT00891748 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2010-01-18

No results posted yet for this study

Summary

The study objective is to evaluate the feasibility of three instillations of immunostimulating gene therapy (AdCD40L) in patients with urinary bladder cancer. Tolerance, toxicity and immunological parameters will be evaluated during and post treatment.

Conditions

Interventions

GENETIC

AdCD40L

Adenovirus vector serotype 5, E1/E3 deletion with human CD40L gene driven by RSV promoter

Sponsors & Collaborators

  • Uppsala University Hospital

    collaborator OTHER
  • Uppsala University

    lead OTHER

Principal Investigators

  • Per-Uno Malmstrom, MD PhD · Uppsala University Hospital, Uppsala, Sweden

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2009-10-31
Completion
2009-10-31

Countries

  • Sweden

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00891748 on ClinicalTrials.gov