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Virus Therapy
VAX014 for Bladder Cancer
Phase 1
Waitlist Available
Research Sponsored by Vaxiion Therapeutics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 28 days
Awards & highlights
Study Summary
This trial is testing a new cancer treatment, called VAX014, to see if it is safe and effective for patients with low-grade bladder cancer.
Eligible Conditions
- Bladder Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 28 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 28 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Incidence of Treatment-Emergence Adverse Events (Safety and Tolerability)
Maximum tolerated dose (MTD) of VAX014
Secondary outcome measures
Anti-Drug Antibodies (Immunogenicity)
Area Under Curve (AUC)
Clearance (Cl)
+7 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: VAX014Experimental Treatment1 Intervention
Intravesical VAX014 (dose: 3.33x10^10 - 9.0x10^11 recombinant bacterial minicells (rBMCs)), given once per week for Weeks 1-6
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
VAX014
2019
Completed Phase 1
~10
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Who is running the clinical trial?
Vaxiion TherapeuticsLead Sponsor
1 Previous Clinical Trials
32 Total Patients Enrolled
Frequently Asked Questions
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