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Chemotherapy
Arm I: R-mabHD for Hodgkin's Lymphoma
Phase 2
Waitlist Available
Led By Prem A Nandiwada, M.D.
Research Sponsored by American Scitech International
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 six months
Awards & highlights
Study Summary
120 subjects with Hodgkin's disease will be randomly divided into two groups: Group I receiving R-mabHD and Group II receiving a combination of Adriamycin,Bleomycin,Vinblastine and Dacarbazine. R-mabHD will be given once a week for eight weeks in a row. The ABVD combination will be given once every other week for 12 treatments. The hypothesis is that intervention with R-mabHD will lead to a quicker remission of Hodgkin's disease than the intervention with a combination of ABVD.
Eligible Conditions
- Hodgkin's Lymphoma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ eighteen months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~eighteen months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
There will be a reduction in the size of the tumor after initiating treatment.
Secondary outcome measures
There will be an improvement in the general condition of the patient and it will be possible to estimate the event free survival rate.
Trial Design
2Treatment groups
Active Control
Group I: Arm I: R-mabHDActive Control1 Intervention
Anti-hodgkin disease agent
Group II: Arm II: ABVDActive Control1 Intervention
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Who is running the clinical trial?
Bristol-Myers SquibbIndustry Sponsor
2,642 Previous Clinical Trials
4,130,003 Total Patients Enrolled
American Scitech InternationalLead Sponsor
5 Previous Clinical Trials
2,690 Total Patients Enrolled
Eli Lilly and CompanyIndustry Sponsor
2,621 Previous Clinical Trials
3,216,502 Total Patients Enrolled
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