Overview

Study of Motexafin Gadolinium for the Treatment of Non-Hodgkin's Lymphoma

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
The primary purpose of this study is to find out if motexafin gadolinium may be an effective treatment for patients with non-Hodgkin's lymphoma (NHL). Secondly, the safety and side effects of motexafin gadolinium will be evaluated.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Pharmacyclics LLC.
Treatments:
Motexafin gadolinium
Criteria
Inclusion Criteria:

- ≥ 18 years old

- Refractory or relapsed indolent NHL. Eligible WHO histologies include follicular NHL
(Grades 1, 2, and 3); marginal zone nodal; marginal zone splenic; and
mucosa-associated lymphoid tissue (MALT) types

- Failed ≥ 1 previous regimens, one of which must have contained rituximab as either a
single agent or in combination with chemotherapy

- ECOG performance status score either 0 or 1

- Willing and able to provide written informed consent

Exclusion Criteria:

Laboratory values of:

- Platelet count < 50,000/µL

- AST or ALT > 2 x the upper limit of normal (ULN)

- Total bilirubin > 2 x ULN

- Creatinine > 2.0 mg/dL

and

- Greater than three prior regimens (where a regimen is defined as a treatment for NHL
given after disease progression)

- Uncontrolled hypertension

- Known history of porphyria, G6PD deficiency, HIV