Clinical Trials Directory

Trials / Terminated

TerminatedNCT00547066

Study of Veltuzumab (hA20) at Different Doses in Patients With ITP

A Phase I/II Study of Immunotherapy With Humanized Anti-CD20 Antibody, IMMU-106 (hA20), in Adult Patients With Chronic Immune Thrombocytopenic Purpura

Status
Terminated
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Gilead Sciences · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This trial will study different dose levels of hA20 (IMMU-106) to see if they are safe and effective for treating ITP.

Detailed description

The goal of current treatment guidelines for most patients with chronic adult ITP is to maintain platelet levels above 30 x 109/L. The conventional first-line therapy is corticosteroids with or without intravenous immunoglobulins, but many patients relapse when steroids are tapered. Standard therapy then is splenectomy, but patients with refractory ITP who do not respond require further therapy. Unfortunately, immunosuppressive agents or other available treatments typically produce only short-term responses. Because of the lack of medical options after first-line therapy, the target population for this first study of anti-CD20 immunotherapy with hA20 are adult patients with chronic ITP who failed at least one standard ITP therapy (i.e., received at least one standard ITP therapy and now present with platelet levels below 30 x 109/L). In autoimmune disease, rituximab as well as other anti-CD20 antibodies currently being considered for commercialization have focused on a different dosing schedule in rheumatoid arthritis, and use fixed dosages rather than variable doses based on body surface area. In addition, recent studies of these newer anti-CD20 antibodies in rheumatoid arthritis have reported that lower doses indeed appear effective when administered twice, 2 weeks apart. Based upon these considerations, patients in this study will receive hA20 twice, 2 weeks apart, and administered at one of 3 dose levels.

Conditions

Interventions

TypeNameDescription
BIOLOGICALveltuzumabhA20 will be administered intravenously in two doses over two weeks

Timeline

Start date
2007-11-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2007-10-19
Last updated
2021-08-16

Locations

8 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00547066. Inclusion in this directory is not an endorsement.