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Completed

NCT Number: NCT00142181

Phase II Study of Campath-1H Antibody to Treat Waldenstrom's Macroglobulinemia

The purpose of this study is to determine the safety and effects (good or bad) of Campath-1H antibody in the treatment of lymphoplasmacytic lymphoma.

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Key information

About this study

  • Patients will receive 3 test doses of Campath-1H (3mg, 10mg, 30mg). If the patient tolerates these three test doses, then they will receive a total of 6 weeks of Campath-1H therapy three times a week.
  • After the patient receives the first 6 weeks of therapy at the 30mg therapeutic dose they will be re-assessed by blood testing. If it is determined that their disease has progressed in the period of time while the patient was on Campath-1H, the patient will be removed from the study.
  • If it is determined that the patient has achieved a complete remission after 6 weeks of Campath-1H treatment a bone marrow biopsy will be performed to confirm complete remission and the patient will not receive any additional treatment but will be followed for a period of 2 years.
  • If the disease has remained stable or partial response has been achieved the patient will enter the second phase of therapy in which they will receive an additional 6 weeks of Campath-1H therapy. The patient will then be reassessed as described above.
  • No additional therapy (as part of this study) will be performed after a 12 week course of Campath-1H.
  • While the patient is on Campath-1H blood test will be performed at 3-6 month intervals over a period extending for 2 years following the last treatment. Bone marrow biopsies and/or aspirations will be conducted as necessary.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of lymphoplasmacytic lymphoma including patients with Waldenstrom's macroglobulinemia
  • Adequate organ function: ANC > 500/ul; PLT > 25,000/ul; serum creatinine < 2.5; serum total bilirubin and SGOT < 2.5 times the upper normal limit.
  • Age greater than 18 years
  • Life expectancy of 6 months or greater
  • ECOG performance status of 0-2

Exclusion criteria

  • Chemotherapy, steroid therapy, or radiation therapy within 21 days of study entry.
  • Prior Campath-1H or monoclonal antibody therapy within 3 months of study entry.
  • Pregnant women
  • Serious co-morbid disease, uncontrolled bacterial, fungal, or viral infection.

Treatment and study plan

Campath-1H

Drug

Participant will receive three test doses of Campath-1H (3, 10, and 30mg). If this is tolerated then they will receive Campath-IH three times a week for 6 weeks.

Primary outcomes

  1. To determine the effectiveness of Campath-1H in treating patients with Waldenstrom's macroglobulinemia.

    Time frame: 2 years

Secondary outcomes

  1. To determine the safety of Campath-1H.

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Dana-Farber Cancer Institute

Other

Collaborators

  • Arizona Oncology Associates
  • Bayer
  • Beth Israel Deaconess Medical Center
  • Brigham and Women's Hospital
  • Massachusetts General Hospital
  • Northwestern University
  • University of California, Los Angeles

Registry information

Official study title

Phase II Study of Campath-1H in Patients With Lymphoplasmacytic Lymphoma (Waldenstrom's Macroglobulinemia)

Important dates

Study start
2003
Primary completion
2005
Study completion
2008
First posted
Sep 2, 2005
Registry last updated
Dec 21, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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