Trial Search Results

Safety Study to Evaluate Monoclonal Antibody KW-0761 in Subjects With Peripheral T-cell Lymphoma

This study will determine the maximum dose of KW-0761 administered intravenously that can be given safely in subjects with previously treated peripheral T-cell lymphoma (PTCL) or cutaneous T-cell lymphoma(CTCL)and will see if it is effective in treating the disease.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Kyowa Hakko Kirin Pharma, Inc.

Intervention(s):

  • Biological: KW-0761

Phase:

Phase 1/Phase 2

Eligibility


Inclusion Criteria:

   1. histologically/cytologically confirmed diagnosis of PTCL including CTCL (including MF
   and SS) but excluding ATLL.

   2. failed at least one prior systemic therapy for PTCL or CTCL.

   3. ECOG PS of <=2 at study entry.

   4. >=18 years of age.

   5. completed any prior therapy at least four weeks prior to entry; however, patients with
   rapidly progressive malignant disease may be enrolled prior to this period after
   discussion with the medical monitor.

   6. resolution of all clinically significant toxic effects of prior cancer therapy to
   grade ≤1 by the NCI-CTCAE, v.3.0 excluding the specifications required in 7 and 8
   below.

   7. adequate hematological function: absolute neutrophil count>=1,500 cells/uL and
   platelets >=100,000 cells/uL except in patients with known bone marrow involvement
   where absolute neutrophil count must be >=1,000 cells/uL and platelets >=75,000
   cells/uL.

   8. adequate hepatic function: bilirubin ≤ 1.5 times the specific institutional ULN;
   aspartate transaminase and alanine transaminase each ≤ 2.5 x ULN or ≤ 5.0 x ULN in the
   presence of known hepatic malignancy.

   9. serum creatinine ≤1.5 x ULN or a calculated creatinine clearance >60 mL/min.

10. CTCL subjects previously treated with zanolimumab are eligible provided their CD4+
   cell counts have recovered to pre-treatment levels.

11. Subjects with MF and a history of staphylococcus colonization are eligible provided
   they continue to receive stable doses of prophylactic antibiotics.

12. provided signed informed consent.

13. WOCBP must have a negative pregnancy test within 7 days of receiving study medication.

14. WOCBP must agree to use effective contraception

15. Male subjects must be willing to use an appropriate method of contraception (e.g.,
   condoms) or abstain from sexual intercourse and inform any sexual partners that they
   must also use a reliable method of contraception during the study.

Exclusion Criteria:

   1. has a significant uncontrolled intercurrent illness including, but not limited to:
   uncontrolled infection requiring antibiotics; clinically significant cardiac disease
   (class III or IV of the New York Heart Association [NYHA] classification); unstable
   angina pectoris; angioplasty, stenting, or myocardial infarction within 6 months;
   uncontrolled hypertension (systolic blood pressure >160 mm Hg, diastolic BP >100 mmHg,
   found on two consecutive measurements separated by a 1-week period) despite two
   anti-hypertensive medications; clinically significant cardiac arrhythmia; or
   uncontrolled diabetes.

   2. has known or tests positive for human immunodeficiency virus (HIV), human T-cell
   leukemia virus (HTLV-1), hepatitis B or hepatitis C.

   3. has evidence of central nervous system (CNS) metastasis.

   4. has received monoclonal antibodies within 6 weeks of study entry.

   5. is pregnant (confirmed by beta human chorionic gonadotrophin [β-HCG]) or lactating.

   6. Subjects on any immunomodulatory drug, (other than low dose corticosteroids equivalent
   to a daily dose of 10 mg of prednisone). Subjects on any immunomodulatory drug within
   4 weeks of their first dose of KW-0761 are also excluded.

   7. has a psychiatric illness, disability or social situation that would compromise the
   subject's safety or ability to provide consent, or limit his or her compliance with
   study requirements.

   8. has experienced allergic reactions to monoclonal antibodies or other therapeutic
   proteins.

   9. Subjects with active herpes simplex or herpes zoster. Subjects with a history of
   herpes zoster who have had an outbreak within the last year will also be excluded.
   Subjects on prophylaxis for herpes who started taking medication at least 30 days
   prior to study entry, should continue to take the prescribed medication for the
   duration of the study.

10. Subjects with known autoimmune diseases. Subjects with Hashimoto's thyroiditis
   controlled with medication are eligible for enrollment.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
650-498-7061
Not Recruiting