Study of SGN-30 (Antibody) in Patients With Refractory or Recurrent Anaplastic Large Cell Lymphoma

• Status: Completed
• Trial end date: 2006-12-01
• Target enrollment: 0
• Participant gender: All

Summary

To investigate safety and antitumor activity of SGN-30 in patients with Hodgkin's Disease and anaplastic large cell lymphoma (ALCL).

As of March 22, 2005, interim analysis of the Hodgkin's Disease (HD) arm has been completed per the statistical plan in the protocol. SG030-0003 is now closed to further recruitment of HD patients.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Seagen Inc.; Seattle Genetics, Inc.
• Treatments: Antibodies; Antibodies, Monoclonal; Brentuximab Vedotin

Criteria

Inclusion Criteria:

• Patients must have refractory or recurrent HD or refractory or recurrent ALCL.

• Patients must have histologically confirmed CD30+ HD or ALCL.

• Patients must have bidimensional measurable disease on physical examination or radiologic evaluation.

• Patients must have failed systemic chemotherapy either as initial therapy for advanced disease or as salvage therapy after initial radiotherapy for early stage disease.

• Patients may have received no more than four treatments (radiation, chemotherapy, and/or biologics) prior to enrollment.

• Patients may have received no more than one stem cell transplantation.

• Patients who have undergone stem cell transplantation must have received at least one therapy post-transplantation. Patients who have not had stem cell transplantation must be considered ineligible or refuse treatment by stem cell transplantation.

• Patients must have completed radiotherapy and/or chemotherapy at least four weeks prior to enrollment. Any prior treatment with nitrogen mustard agents, melphalan, or BCNU must have been completed at least six weeks prior to enrollment.

• Patients must have an ECOG performance status of ≤ 2 and a life expectancy > three 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 β-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. A copy of the signed informed consent form will be retained in the patient's chart.

• Patients must meet baseline lab data requirements.

Exclusion Criteria:

• Patients with primary cutaneous ALCL

• Patients who have been treated previously with any anti-CD30 antibody

• Patients who have received any mAb unless a recent serum testing reveals no antibody titer and no evidence of human anti-murine antibodies (HAMA) or human anti-chimeric antibodies (HACA) in the peripheral circulation

• Patients receiving any investigational biological agent within eight weeks of enrollment or any other investigational agent within four weeks of enrollment

• 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 known active viral, bacterial, or systemic fungal infection; patients who are known to be HIV, Hepatitis B, or Hepatitis C positive.

• Patients with symptomatic cardiac disease including ventricular dysfunction, coronary artery disease, or arrhythmias

• Patients with symptomatic brain metastases requiring treatment

• 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