Trial record 1 of 1 for:    Immunotherapy with hLL1-DOX
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Phase I/II Study of hLL1-DOX in Relapsed NHL and CLL

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2014 by Immunomedics, Inc.
Sponsor:
Information provided by (Responsible Party):
Immunomedics, Inc.
ClinicalTrials.gov Identifier:
NCT01585688
First received: April 23, 2012
Last updated: May 7, 2014
Last verified: May 2014
  Purpose

The primary objectives are to evaluate the safety and tolerability of hLL1-DOX, and to determine the maximum tolerated dose (MTD) regimen (in terms of a dose and its associated dosing schedule). The secondary objectives are to obtain information on efficacy, pharmacodynamics, pharmacokinetics, and immunogenicity, and to determine the optimal dose for subsequent studies.


Condition Intervention Phase
Non-Hodgkin's Lymphoma
Chronic Lymphocytic Leukemia
Drug: hLL1-DOX (IMMU-115)
Phase 1
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Phase I/II Study of Immunotherapy With hLL1-DOX in Patients With Non-Hodgkin's Lymphoma (NHL) and Chronic Lymphocytic Leukemia (CLL)

Resource links provided by NLM:


Further study details as provided by Immunomedics, Inc.:

Primary Outcome Measures:
  • Safety [ Time Frame: during treatment and the change at 4, 8 & 12 weeks after treatment ] [ Designated as safety issue: Yes ]
    Safety will be measured by physical examinations and hematology and chemistry blood tests. Cardiac safety will be done using MUGA scans or echocardiograms. These assessments will be done routinely during treatment and again 4, 8 and 12 weeks after treatment. Long term safety will be assessed every 3 months after that for up to 2 years.

  • Efficacy [ Time Frame: During treatment and the changes at 4, 8 and 12 weeks after treatment ] [ Designated as safety issue: No ]
    Efficacy will be assessed using CT scans for NHL patients and CT scans and hematology labs for CLL patients. At the beginning of a complete response a repeat bone marrow biopsy may be required. These assessments will be done 8 weeks after the start of treatment and again 10-12 weeks later at the end of treatment. The tests will be repeated at 4, 8 and 12 weeks after treatment and then every 3 months for up to 2 years.


Estimated Enrollment: 30
Study Start Date: August 2012
Estimated Study Completion Date: February 2017
Estimated Primary Completion Date: November 2016 (Final data collection date for primary outcome measure)
Intervention Details:
    Drug: hLL1-DOX (IMMU-115)
    hLL1-DOX is administered intravenously at one of 4 dose levels on days 1, 4, 8 and 11 of 21-day treatment cycles, with up to 8 cycles administered.
    Other Name: IMMU-115
Detailed Description:

Patients receive hLL1-DOX at one of 4 dose levels administered on Days 1, 4, 8 and 11 of 21-day treatment cycles which are continued in the absence of progression or unacceptable toxicity up to a total of 8 cycles. After treatment, follow-up will be done at 4, 8 and 12 weeks post-treatment and will continue to be done every 3 months for up to 2 years.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female, age ≥ 18 years
  • Able to provide signed, informed consent
  • Histologically confirmed diagnosis of recurrent B-cell non-Hodgkin's lymphoma (any histology by WHO criteria) or recurrent chronic lymphocytic leukemia (by NCI criteria) (Reference Appendix C)
  • Received at least one prior treatment with standard therapy (previous antibody therapy is acceptable)
  • Measurable disease at least one lesion ≥ 1.5 cm for NHL and ALC > 5,000 for CLL
  • Adequate performance status (≥ 70 Karnofsky scale) with an estimated life expectancy of at least 6 months

    --Documented negative hepatitis B screen, per NCCN guidelines (hepatitis B surface antigen/antibodies, core antigen/antibodies, hepatitis B e-antigen)

  • At least 12 weeks beyond stem cell transplant and 4 weeks beyond chemotherapy or immunotherapy, major surgery, other experimental treatments, or radiation therapy to the index lesions, and with all acute toxicities from prior therapy resolved to less than Grade 2 toxicity by NCI CTC version 4.0
  • Laboratory parameters:

Adequate hematology without ongoing transfusional support Hemoglobin >/= 10 g/dL Absolute neutrophil count >/= 1.5 x 10 9/L Platelets >/= 75 x 10 9/L Creatinine and bilirubin </= 1.5 x IULN AST and ALT </= 2.5 x IULN

-Adequate cardiac function (MUGA scan or 2-D ECHO with LVEF ≥ 55%, EKG with no medically relevant arrhythmia uncontrolled on medications)

Exclusion Criteria:

  • -Pregnant or lactating women. Women of childbearing potential must have a negative pregnancy test. Pregnancy testing is not required for post-menopausal or surgically sterilized women.
  • Women of childbearing potential and fertile men who are not practicing or who are unwilling to practice birth control while enrolled in the study until at least 12 weeks after the last milatuzumab infusion
  • Prior therapy with other human or humanized monoclonal antibodies, unless HAHA tested and negative
  • Prior treatment with trastuzumab
  • Bulky disease by CT, defined as any single mass > 10 cm in its greatest diameter
  • Known HIV positive or active hepatitis B or C, or presence of hepatitis B surface antigens or presence of hepatitis C antibody
  • New York Heart Classification III or IV heart disease (see Appendix G). Other severe cardiovascular or cardiopulmonary disease, including COPD
  • Baseline BNP > 2 x IULN
  • Patients with uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities will be excluded
  • Patients with recent (≤ 6 months) cardiac angina, difficult to control congestive heart failure, uncontrolled hypertension, or difficult to control cardiac arrhythmias will be excluded
  • Known autoimmune disease or presence of autoimmune phenomena
  • At least 7 days beyond any infection requiring intravenous antibiotic use (Oral antibiotics may be administered prophylactically as clinically indicated)
  • Systemic corticosteroids within 2 weeks, except low dose regimens (prednisone, ≤ 20 mg/day, or equivalent) which may continue if unchanged
  • Substance abuse or other concurrent medical or psychiatric conditions that, in the Investigator's opinion, could confound study interpretation or affect the patient's ability to tolerate or complete the study
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01585688

Contacts
Contact: Anne Johnson, RN 973-605-8200 ajohnson@immunomedics.com
Contact: Jon Rojo 973-605-8200 jrojo@immunomedics.com

Locations
United States, Delaware
Helen F. Graham Cancer Center Recruiting
Newark, Delaware, United States, 19713
Contact: Kathy Combs, RN       kcombs@christianacare.org   
Principal Investigator: Michael Guarino, MD         
United States, Florida
MD Anderson Cancer Center Orlando Recruiting
Orlando, Florida, United States, 32806
Contact: Casey Kulscar, RN       casey.kulscar@orlandohealth.com   
Principal Investigator: Julio Hajdenberg, MD         
United States, Indiana
IU Health Goshen Center for Cancer Care Recruiting
Goshen, Indiana, United States, 46526
Contact: Tracy Thorne       tthorne@iuhealth.org   
Principal Investigator: Alexander Starodub, MD         
United States, Massachusetts
UMass Memorial Cancer Center of Excellence Recruiting
Worcester, Massachusetts, United States, 01605
Contact: Volkan Cetin       volkan.cetin@umassmemorial.org   
Principal Investigator: Andrew Evens, DO         
United States, New Jersey
John Theurer Cancer Center Hackensack University Medical Center Recruiting
Hackensack, New Jersey, United States, 07601
Contact: Kara Yannotti, RN       kyannotti@hackensackumc.org   
Principal Investigator: Andre Goy, MD         
United States, Texas
U.T. MD Anderson Cancer Center Houston Recruiting
Houston, Texas, United States, 77030
Contact: Linda Claret, RN       lcclaret@mdanderson.org   
Principal Investigator: Felipe Samaniego, MD         
Sponsors and Collaborators
Immunomedics, Inc.
  More Information

No publications provided

Responsible Party: Immunomedics, Inc.
ClinicalTrials.gov Identifier: NCT01585688     History of Changes
Other Study ID Numbers: IM-T-hLL1-DOX-02
Study First Received: April 23, 2012
Last Updated: May 7, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Immunomedics, Inc.:
NHL
CLL

Additional relevant MeSH terms:
Leukemia
Leukemia, Lymphocytic, Chronic, B-Cell
Leukemia, Lymphoid
Lymphoma
Lymphoma, Non-Hodgkin
Immune System Diseases
Immunoproliferative Disorders
Leukemia, B-Cell
Lymphatic Diseases
Lymphoproliferative Disorders
Neoplasms
Neoplasms by Histologic Type

ClinicalTrials.gov processed this record on October 29, 2014