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Metformin and Simvastatin Treatment for Bladder Cancer

Phase 2
Waitlist Available
Led By Jonathan Izawa, MD
Research Sponsored by London Health Sciences Centre
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 the participant will be followed for the duration of the pre-surgical preparation period. this is expected to be fewer than 12 weeks
Awards & highlights
Approved for 20 Other Conditions
No Placebo-Only Group
All Individual Drugs Already Approved

Summary

A single arm, single center window of opportunity trial of using a combination of metformin and simvastatin as a neoadjuvant treatment for patients with invasive bladder cancer who are to undergo cystectomy. The study will assess the feasibility of conducting window of opportunity trials in invasive bladder cancer the drug combination's affects on a variety of important clinicopathologic variables. The goal is to enroll 44 patients within 18 months. An interim analysis will be conducted at 12 months, and the study will be prematurely closed if fewer than 10 patients have been enrolled at that time. Patients will be administered 850mg of metformin twice daily along with 20mg of Simvastatin. Patients will be enrolled following the formal diagnosis of invasive bladder cancer or at first visit following referral to the London Health Sciences Center (LHSC). Patient's will receive metformin and simvastatin from the time of enrollment until the night prior to their operation in the absence of safety or tolerability concerns.

Eligible Conditions
  • Bladder Cancer

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~the participant will be followed for the duration of the pre-surgical preparation period. this is expected to be fewer than 12 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and the participant will be followed for the duration of the pre-surgical preparation period. this is expected to be fewer than 12 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Bladder tumor proliferation rate
Feasibility of performing neoadjuvant window of opportunity trials using drugs with potential bioactivity against invasive bladder cancer
Secondary study objectives
Impact of Metformin and Simvastatin therapy on the signalling pathways involved in invasive urothelial carcinoma.
Level of apoptosis observed in tumor cells of patients who undergo Metformin and Simvastatin therapy before cystectomy.
Toxicity in patients who participate in the treatment regimen of Metformin and Simvastatin therapy

Awards & Highlights

Approved for 20 Other Conditions
This treatment demonstrated efficacy for 20 other conditions.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Metformin and Simvastatin TreatmentExperimental Treatment2 Interventions
Patients in this group will receive 850 mg of Metformin and 20 mg of Simvastatin daily from the time they are enrolled in the study until the day before their surgery (approximately 12 weeks), in the absence of any safety or tolerability concerns.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Simvastatin
FDA approved
Metformin
FDA approved

Find a Location

Who is running the clinical trial?

London Health Sciences CentreLead Sponsor
146 Previous Clinical Trials
52,310 Total Patients Enrolled
Jonathan Izawa, MDPrincipal InvestigatorLondon Health Sciences Centre
1 Previous Clinical Trials
300 Total Patients Enrolled
~4 spots leftby Nov 2025