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Cell Therapy

1 for Cardiomyopathy (CAuSMIc II Trial)

Phase 2
Waitlist Available
Research Sponsored by Mytogen, Inc.
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 12 months
Awards & highlights

CAuSMIc II Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of injecting myoblasts (grown from your own skeletal muscle), using a catheter device, directly into the damaged heart muscle for treatment of severe heart failure.

Eligible Conditions
  • Cardiomyopathy

CAuSMIc II Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 12 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Kansas City Cardiomyopathy Questionnaire
Secondary outcome measures
Cardiovascular mortality

CAuSMIc II Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: 1Experimental Treatment1 Intervention
myoblast
Group II: 2Placebo Group1 Intervention
sham injection procedure

Find a Location

Who is running the clinical trial?

Mytogen, Inc.Lead Sponsor

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Study to Assess the Efficacy and Safety of Transplanting Autologous Skeletal Myoblasts, Into Infarcted Heart, Using an Catheter Delivery System
2008. "Study to Assess the Efficacy and Safety of Transplanting Autologous Skeletal Myoblasts, Into Infarcted Heart, Using an Catheter Delivery System". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT00626314.
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