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Phase 2
18 Years
75 Years
Open (Enrolling)
Multiple Myeloma, Non-hodgkin's Lymphoma, Hodgkin's Disease

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Trial Information

Inclusion Criteria:

- Male or female 18 to 75 years of age inclusive;

- Patients with confirmed pathology diagnosis of MM, NHL or HD;

- Potential candidate for autologous stem cell transplantation at Investigator's

- 4 weeks since last cycle of chemotherapy prior to the study drug administration;

- Total dose of melphalan received 200 mg in the most recent chemotherapy treatment;

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;

- Recovered from all acute toxic effects of prior chemotherapy at Investigator's

- White blood cell (WBC) count 3.0 x 109/L on screening laboratory assessments;

- Absolute neutrophil count 1.5 x 109/L on screening laboratory assessments;

- Platelet count 100 x 109/L on screening laboratory assessments;

- Serum creatinine 2.2 mg/dL on screening laboratory assessments;

- Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and total bilirubin
< 2 x upper limit of normal (ULN) on screening laboratory assessments;

- Negative for human immunodeficiency virus (HIV);

- Adequate cardiac and pulmonary function to undergo leukapheresis at Investigator's

- For females, one of the following criteria must be fulfilled:

1. At least one year post-menopausal, or

2. Surgically sterile, or

3. Willing to use a double-barrier method [intrauterine device (IUD) plus condom,
spermicidal gel plus condom] of contraception from study Day 1 until 28 days
after the last dose of TG-0054;

- Males must be willing to use a reliable form of contraception (use of a condom or a
partner fulfilling the above criteria) from study Day 1 until 28 days after the last
dose of TG-0054;

- Able to provide the signed informed consent.

Exclusion Criteria:

- Received radiation therapy to the pelvis;

- Received > 6 cycles of lenalidomide;

- Evidence of bone marrow involvement of lymphoma in NHL patients;

- Failed previous stem cell collection [failed to collect 2 x 106 CD34+ cells/kg within
4 leukapheresis sessions after receiving granulocyte colony-stimulating factor

- Patients who have undergone previous stem cell transplantation procedure;

- Received G-CSF within 2 weeks prior to the study drug administration;

- History of other cancer within the past 5 years excluding MM, NHL, HD, basal cell or
squamous cell carcinoma of the skin;

- History of other hematologic disorders including bleeding or thromboembolic disease
being treated with anti-coagulant;

- History of poor and uncontrollable cardiovascular or pulmonary disease such as
myocardial infarction, cardiac arrhythmias, transient ischemic attack, stroke or
Chronic Obstructive Pulmonary Disease (COPD) patients hospitalized more than two
times a year due to underlying disease;

- Diagnosis of sickle cell anemia or documented sickle cell trait;

- Patients with proliferative retinopathy;

- Uncontrollable malignancy with MM, NHL or HD, or carcinomatous meningitis, at
Investigator's discretion;

- Any infection required antibiotic treatment or unexplained fever above 38 °C within 3
days prior to dosing;

- Pregnant or breast-feeding;

- Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for
treatment of either a psychiatric or physical (e.g., infectious disease) illness must
not be enrolled into this study;

- Received any other investigational drug within 1 month before entering the study;

- Received prior treatment with TG-0054 but withdrew early from this study.

Type of Study:


Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

To determine the total number of HSCs collected within four leukapheresis sessions after TG-0054 (3.14 mg/kg) alone or in combination with G-CSF mobilization in patients with Multiple Myeloma, Non-Hodgkin Lymphoma or Hodgkin Disease

Outcome Time Frame:

1 week

Safety Issue:


Principal Investigator

Michael W. Schuster, M.D.

Investigator Role:

Principal Investigator

Investigator Affiliation:

Stony Brook University Hospital


United States: Food and Drug Administration

Study ID:




Start Date:

December 2011

Completion Date:

December 2013

Related Keywords:

  • Multiple Myeloma
  • Non-Hodgkin's Lymphoma
  • Hodgkin's Disease
  • Hodgkin Disease
  • Lymphoma
  • Lymphoma, Non-Hodgkin
  • Multiple Myeloma
  • Neoplasms, Plasma Cell



Stony Brook University Hospital Stony Brook, New York  11794-8174