Status:
COMPLETED
Study of SGN-30 (Anti-CD30 mAb) in Patients With Primary Cutaneous Anaplastic Large Cell Lymphoma
Lead Sponsor:
Seagen Inc.
Conditions:
Large Cell Lymphoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This multi-center, phase II study will be conducted to define the toxicity profile and antitumor activity of SGN-30 in patients with pcALCL and other closely related lymphoproliferative disorders.
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Patients must have a definite diagnosis.
- Patients must be histologically confirmed CD30 positive within 3 months of enrollment
- Patients with pcALCL must have target lesions present for at least 1 month without spontaneous regression
- pcALCL patients must have failed treatment with local radiation therapy, or failed systemic therapy of a single agent
- Patients must be considered an eligible candidate for systemic therapy as determined by the investigator
- All patients must have a three week wash-out from previous treatments, unless in the opinion of the investigator it is not in the best interest of the patient, at which point the individual case must be discussed with the medical monitor prior to enrollment.
- Patients must have an ECOG performance status of \< 2 (Appendix B) and a life expectancy \> six months.
- Patients must be at least 18 years of age.
- Patients must be available for periodic blood sampling, study-related assessments, and management of toxicity at the treating institution.
- Females of childbearing potential must have a negative HCG pregnancy test result within three days of enrollment. All patients must agree to use an effective contraceptive method during the course of the study.
- Patients must give written informed consent.
- Required baseline laboratory data: Absolute neutrophil count greater than or equal to to 1,000/mm3, Platelet count greater than or equal to 75,000/mm3, Serum bilirubin less than or equal to 1.5 times ULN, Serum creatinine less than or equal to 1.5 times ULN, BUN less than or equal to 1.5 times ULN, SGOT less than or equal to 2.5 ULN, SGPT less than or equal to 2.5 ULN
- Criteria for Exclusion
- Patients with Sezary syndrome, or any type of lymphoproliferative disease other than pcALCL, T-MF or LyP
- Patients with systemic ALCL or extracutaneous involvement of cutaneous ALCL
- Patients with known active systemic viral, bacterial, or fungal infection
- Patients who are known to be HIV, Hepatitis B, or Hepatitis C positive
- Patients who have been treated previously with any anti-CD30 antibody
- Patients with a known hypersensitivity to recombinant proteins or any excipient contained in the drug formulation
- Patients with a history of other malignancies during the past five years with the exception of adequately treated basal or squamous cell skin cancer or cervical carcinoma in situ
- Patients with symptomatic cardiac disease including ventricular dysfunction, coronary artery disease, or arrhythmias
- Patients who are pregnant or breastfeeding
- Patients with any serious underlying medical condition that would impair their ability to receive or tolerate the planned treatment
- Patients with dementia or altered mental status that would preclude understanding and rendering of informed consent
Exclusion
Key Trial Info
Start Date :
September 1 2004
Trial Type :
INTERVENTIONAL
End Date :
February 1 2007
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT00099255
Start Date
September 1 2004
End Date
February 1 2007
Last Update
December 18 2014
Active Locations (13)
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1
University of Alabama at Birmingham
Birmingham, Alabama, United States, 35294
2
University of California at Los Angeles
Los Angeles, California, United States, 90095
3
Stanford University
Stanford, California, United States, 94305
4
Yale
New Haven, Connecticut, United States, 06520