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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 weeks
Treatment ~ Varies
Follow Up ~up to 28 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 28 days for reporting.

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 more

Trial 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

Find a Location

Who is running the clinical trial?

Vaxiion TherapeuticsLead Sponsor
1 Previous Clinical Trials
32 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~1 spots leftby Apr 2025