The purpose of the study is to investigate the safety of the investigational agent, cirmtuzumab. Cirmtuzumab is a monoclonal antibody drug designed to attach to a protein, called ROR1, on the surface of chronic lymphocytic leukemia (CLL) cells to block cell growth and survival. ROR1 is rarely expressed on healthy cells so the idea is to preferentially get rid of the cancer cells. Although there is evidence in laboratory animals that cirmtuzumab can decrease the number of CLL cells, the investigators do not know if this will work in humans. This drug will be given to humans for the first time in this study. Therefore, the goal of this study is to see if cirmtuzumab is safe and tolerated in study participants.

This is a first in human, open-label single institution, Phase I dose escalation study of in patients with relapsed or refractory CLL. Treatment cycle (14 days) will consist of cirmtuzumab administered intravenously on a bi-weekly (every two weeks) schedule for a total of 4 doses. Eight dose cohorts (of 3 to 6 patients in size) plus an expansion cohort of 6 patients are planned. In the first 4 dose cohorts, there is intra-patient dose escalation to monitor for acute toxicities, such as tumor lysis syndrome.

A cycle may be repeated every 14 days if the patient has at least stable disease by clinical examination (or interim response assessment) and has again met hematologic, renal, and hepatic laboratory parameters as defined in the eligibility section, and is without ongoing Grade 3 non-hematologic or Grade 4 hematologic toxicities attributable to cirmtuzumab. The total duration of study drug administration is 4 cycles. Each cycle consists of clinical and laboratory evaluation on Day 1 and safety assessments on Days 3 and 8.

INCLUSION CRITERIA:

• Clinical and phenotypic verification of B cell CLL and measurable disease. Immunophenotyping of the leukemic cells must demonstrate a monoclonal B cell population with immunophenotype consistent with CLL.

• Relapsed or refractory disease, defined by failure to achieve a partial response within 6 months of initiation of therapy, or a 50% increase of baseline disease measurements after achieving a clinical response.

• Not amenable to approved therapies.

• Prior Therapy: Must have progressed after purine-analog or alkylator based therapy, or be considered inappropriate for chemo-immunotherapy due to one of the following:

  • Del 17p, which is associated with poor response to chemo-immunotherapy, or
  • Age greater than 70, or
  • Age greater than 65 with one of the following:
  • Grade ≥ 3 neutropenia, anemia, or thrombocytopenia attributable to cumulative myelotoxicity from prior administration of cytotoxic agents (as documented by bone marrow biopsy obtained since last prior therapy), or
  • Clinically apparent autoimmune cytopenia which may be exacerbated by fludarabine therapy, or
  • Estimated creatinine clearance (eCCr) <70 mL/min (as determined by the Cockcroft-Gault method), or
  • Eastern Cooperative Oncology Group (ECOG) performance status greater than 0.

• Has recovered from the toxic effects of prior therapy to their clinical baseline.

• Women of childbearing potential must agree not to become pregnant for the duration of the study. Both men and women must agree to use a barrier method of contraception for the duration of the study and until 10 weeks after the final dose of cirmtuzumab.

• Subjects must have at least one of the following indications for treatment:

  • Symptomatic or progressive splenomegaly;
  • Symptomatic lymph nodes, nodal clusters, or progressive lymphadenopathy;
  • Progressive anemia (hemoglobin ≤ 11 g/dL);
  • Progressive thrombocytopenia (platelets ≤ 100 x 10^9/L);
  • Weight loss > 10% body weight over the preceding 6 month period;
  • Fatigue attributable to CLL;
  • Fever or night sweats for > 2 weeks without evidence of infection;
  • Progressive lymphocytosis with an increase of > 50% over a 2-month period or an anticipated doubling time of less than 12 months.

• Subjects must have an ECOG performance status of 0-2.

• Adequate hematologic function

• Adequate renal function

• Adequate hepatic function

• Adequate coagulation tests

EXCLUSION CRITERIA:

• Pregnant or breast-feeding women will not be entered on this study due to risks of fetal and teratogenic adverse events as seen in animal/human studies.

• Patients who are currently receiving another investigational agent are excluded.

• Patients who have had chemotherapy (e.g., purine analogues, alkylating agents), immunotherapy, radiation therapy, or participation in any investigational drug treatment within 4 weeks of initiation of UC-961 or at any time during the study.

• Patients who have had prior (within 8 weeks of initiation of UC-961) or concurrent antibody therapy directed against CLL (i.e., Rituxan® and Campath®).

• Current infection requiring parenteral antibiotics.

• Active infection with HIV, hepatitis B virus (HBV), or hepatitis C virus (HCV).

• Concurrent malignancy or prior malignancy within the previous 3 years (other than completely resected carcinoma in situ, prostate cancer, or localized non-melanoma skin cancer).

• Known central nervous system (CNS) involvement by malignancy.

• Untreated autoimmunity such as autoimmune hemolytic anemia, or immune thrombocytopenia.

• Uncompensated hypothyroidism (defined as thyroid-stimulating hormone (TSH) greater than 2x upper limit of normal not treated with replacement hormone).

• Presence of more than 55% pro-lymphocytes in peripheral blood. Patients with Richter's transformation are not excluded.

• Insufficient recovery from surgical-related trauma or wound healing.

• Impaired cardiac function including any of the following:

  • Myocardial infarction within 6 months of starting study drug;
  • A past medical history of clinically significant ECG abnormalities, including QTc 481 milliseconds or greater;
  • Other clinically significant heart disease (e.g., congestive heart failure, uncontrolled hypertension, history of labile hypertension, or history of poor compliance with an antihypertensive regimen).

Twenty-seven subjects were treated with cirmtuzumab and are included in the primary outcome analysis. One subject was enrolled into the trial twice; first in Cohort 1 and then again in Cohort 4 and is counted twice for the baseline characteristics.

Adverse events collected from the start of the first infusion of cirmtuzumab to the last subject's final visit in long-term follow-up (on average 3 years 8 months)

Note that some patients elected to enroll in extension study (ClinicalTrails.gov record #NCT02860676) and therefor the cut-off date for some may be the date patient was first treated on extension protocol. Timeframe for this result therefore difficult to reconcile as asked to report here.

Note no deaths observed during the timeframe of the study observation period.

Some patients enrolled in extension study (#NCT02860676)& cut-off date for AE observation may be date patient was first treated on extension, therefor AE Timeframe period difficult to reconcile. 0 deaths observed during study observation period.