Study Comparing R-mabHD and a Combination of ABVD in Hodgkin's Disease

Hodgkin's Disease Clinical Trial

Official title:

A Phase II Open Label, Multicenter, Randomized, Parallel Study Comparing the Efficacy of R-mabHD Alone and a Combination of Adriamycin, Bleomycin, Vinblastine and Dacarbazine (ABVD)in Treating Patients With Hodgkin's Disease.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT00797472
• Other study ID #: ASI-HDII 1108
• Status: Not yet recruiting
• Phase: Phase 2
• First received: November 24, 2008
• Last updated: July 19, 2011
• Start date: July 2011
• Est. completion date: April 2014

Study information

• Verified date: July 2011
• Source: American Scitech International
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial 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.

Description:

The primary objective is to compare the efficacy of R-mabHD with a combination therapy of Adriamycin, Bleomycin,Vinblastine and Dacarbazine (ABVD) in bringing about remission of Hodgkin's lymphoma and reduction in tumor size.

Primary Study Endpoint: Primary efficacy criterion is percentage of patients achieving a functional score of 1.

Efficacy evaluation is based on assessment of functional score. At the end of six months, a functional assessment of the tumor will be undertaken to record the score as follows:

Score 1: >/= 50% reduction in size of tumor Score 2: < 50% reduction in size of tumor.

Secondary Study Endpoint: Additional secondary endpoint is the average time to achieve 50% reduction in size of tumor.

120 subjects with Hodgkin's Disease will be divided randomly into two groups. 60 subjects (Group I)will receive R-mabHD by intravenous infusion in a dose of 375mg/m2 once a week for eight weeks in a row. The other half (Group II) will receive a combination of intravenous Adriamycin, Bleomycin, Vinblastine and Dacarbazine every other week for 12 treatments. Enrollment period will be three years and subjects from both genders will be accepted. Subjects should be between the ages of 18 and 65. No healthy volunteers will be accepted. Females who are nursing babies or are pregnant will be excluded from the study. Subjects will be evaluated every month for the first six months and then at one year and then at eighteen months after the baseline visit one.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 120
• Est. completion date: April 2014
• Est. primary completion date: April 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Must sign an informed consent form

2. Must have histologically proven diagnosis of Hodgkin's lymphoma

3. Both genders and age between 18 and 65

4. Must have adequate bone marrow reserve (ANC.1500/mm3, Platelet>50,000/mm3)

5. Must have bidimensionally measureable disease

6. LVEF >50% by echocardiogram

7. Serum creatinine upto one fold

8. Serum bilirubin upto one fold

9. Hepatitis B surface antigen negative

10. Hodgkin's Disease patients who relapse after radiation therapy alone or surgical treatment alone or both,or previously untreated patients with stage II bulky, III and IV.

Exclusion Criteria:

1. HIV positive

2. Pregnant women and women of child bearing age who are not practising adequate contraception

3. Severe pulmonary disease including COPD and asthma

4. Evidence of other malignancy except superficial nonmelanoma skin carcinoma or carcinoma in situ of the cervix

5. Nursing mothers

6. Uncontrolled active infection

7. concurrent prednisone or other systemic steroid therapy

8. Less than 4 weeks since prior radiotherapy

9. Less than 30 days since prior investigational therapy.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Hodgkin Disease
• Hodgkin's Disease

Intervention

Drug:
• R-mabHD
An intravenous infusion containing R-mabHD 375mg/m2 will be administered over a period of 3 to 8 hours every week for eight weeks in a row.
• ABVD
A combination of Adriamycin, Bleomycin, Vinblastine and Dacarbazine (ABVD) will be given intravenously over a period of 3 hours every other week for 12 treatments.

Locations

Country	Name	City	State
United States	Raritan Bay Medical Center	Englishtown	New Jersey

Sponsors (3)

Lead Sponsor	Collaborator
American Scitech International	Bristol-Myers Squibb, ImClone LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	There will be a reduction in the size of the tumor after initiating treatment.		Six months	Yes
Secondary	There will be an improvement in the general condition of the patient and it will be possible to estimate the event free survival rate.		Eighteen months	Yes