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| Sponsor: | Genmab |
|---|---|
| Information provided by: | Genmab |
| ClinicalTrials.gov Identifier: | NCT00092274 |
Purpose
The purpose of this trial is to determine the safety and efficacy of HuMax-CD20 as a treatment for Follicular Lymphoma (FL).
| Condition | Intervention | Phase |
|---|---|---|
|
Lymphoma, Follicular |
Drug: HuMax-CD20 |
Phase I Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Dose Comparison, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | An Open-Label, International, Multicenter, Dose Escalating, Phase I/II Study of HuMax-CD20 in Patients With Relapsed or Refractory Follicular Lymphoma Grade I-II |
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Received the following treatments within 4 weeks prior to entering this study:
Contacts and Locations
More Information
| Study ID Numbers: | Hx-CD20-001 |
| Study First Received: | September 22, 2004 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00092274 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Follicular Lymphoma Non Hodgkin´s Lymphoma |
|
Lymphatic Diseases Neoplasms Immunoproliferative Disorders Neoplasms by Histologic Type Immune System Diseases |
Lymphoma, Follicular Lymphoma, Non-Hodgkin Lymphoproliferative Disorders Lymphoma |