Non Hodgkin Lymphoma Clinical Trial

Dose Ranging Trial for Pixantrone in the FND-R Variant Regimen in Indolent Non-Hodgkin’s Lymphoma

Summary

The aim of this trial is to determine the appropriate dose of pixantrone to be used in this combination and obtain data on the combination's safety and activity profile.

View Full Description

Full Description

The FND-R regimen is commonly used in the treatment of indolent Non-Hodgkin's lymphoma (NHL) and contains the chemotherapy agents mitoxantrone, fludarabine, dexamethasone (a steroid) and the monoclonal antibody rituximab. In this trial we are replacing mitoxantrone with pixantrone, an agent with a similar chemical structure (both agents are DNA intercalators). The trial is being run in patients with relapsed or refractory indolent NHL and aims to define the appropriate dose of pixantrone to be used in this combination, as well as to obtain data on pixantrone's safety and activity profile in combination with these drugs.

This trial is expected to recruit up to 30 patients in the USA. Patients will be treated with the drug combination for up to eight months and then followed closely in the four-week period after the last administration. After that, patients will receive physician check-ups every three months.

View Eligibility Criteria

Eligibility Criteria

Inclusion criteria

Patients with relapsed or refractory indolent (low-grade) NHL
Who have received 1-3 prior treatments with chemotherapy

Exclusion criteria

Patients previously treated with fludarabine
Prior treatment with rituximab (Rituxan), unless there was a complete response (CR) or partial response (PR) to that treatment
Patients known to have an allergic reaction to rituximab, or to murine proteins.

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 1

Estimated Enrollment:

30

Study ID:

NCT00060684

Recruitment Status:

Completed

Sponsor:

CTI BioPharma

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 4 Locations for this study

See Locations Near You

Arizona Clinical Research Center
Tucson Arizona, 85712, United States
Greater Baltimore Medical Center
Baltimore Maryland, 21204, United States
New Mexico Onc/Hem Consultants, Inc.
Albuquerque New Mexico, 87109, United States
MD Anderson Cancer Center
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 1

Estimated Enrollment:

30

Study ID:

NCT00060684

Recruitment Status:

Completed

Sponsor:


CTI BioPharma

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider