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Virus Therapy
Open Label for Breast Cancer
Phase 2
Waitlist Available
Led By Steven J Isakoff, MD PhD
Research Sponsored by Rogers Sciences Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Histologically or cytologically confirmed Stage IIIb or IV breast cancer with cutaneous metastases.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 23
Awards & highlights
Study Summary
The purpose of this Phase II study is to evaluate the efficacy and safety of Continuous Low- Irradiance Photodynamic Therapy (CLIPT) when used with Verteporfin in the treatment of cutaneous metastases of breast cancer for which no curative or significantly palliative therapy exists, including chest wall therapy.
Eligible Conditions
- Breast Cancer
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 23
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 23
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Objective Response Rate
Trial Design
1Treatment groups
Experimental Treatment
Group I: Open LabelExperimental Treatment2 Interventions
Continuous Low-Irradiance Photodynamic Therapy (CLIPT) Using Verteporfin
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Verteporfin
FDA approved
Find a Location
Who is running the clinical trial?
Rogers Sciences Inc.Lead Sponsor
3 Previous Clinical Trials
30 Total Patients Enrolled
1 Trials studying Breast Cancer
3 Patients Enrolled for Breast Cancer
Steven J Isakoff, MD PhDPrincipal InvestigatorMassachusetts General Hospital
Frequently Asked Questions
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