Study of GO-203-2C Given Intravenously in Patients With Advanced Solid Tumors Including Lymphomas

Completed · Phase 1

Conditions studied: Solid Tumors

In brief

This clinical trial is about testing GO-203-2c, which is a newly discovered compound that binds to an oncoprotein (a cancer causing protein) called MUC1 (which is over-expressed in many cancers). By binding to MUC1, GO-203-2c eventually causes tumor cell death in laboratory studies. This study is being done to: * Test the safety of GO-203-2c and see what effects (good and bad) it has on you and your cancer * Find the highest dose of GO-203-2c that can be given without causing bad side effects * Examine how much GO-203-2c is in the blood at certain times after it is given and how quickly the body gets rid of it * Observe whether there is any effect of GO-203-2c on the size and activity of cancer in your body

Key facts

Study ID

NCT01279603

Run by

Genus Oncology, LLC

People needed

23

Starts

2011-01-01

Expected to finish

2013-05-01

Last updated by the study team

2014-09-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically confirmed solid tumors or lymphomas
• Tumor progression observed after receiving standard/approved systemic chemotherapy and/or immunotherapy including monoclonal antibodies, or when there is no approved or effective therapy
• One or more measureable tumors by radiological evaluation
• Karnofsky performance ≥ 70%
• Life expectancy of ≥ 3 months
• Age ≥ 18 years
• Signed, written IRB-approved informed consent
• Negative pregnancy test (if female)
• Adequate liver function:
• Bilirubin less than or equal to 1.5 x upper limit of normal (ULN)
• AST (SGOT), ALT (SGPT) and Alkaline phosphatase less than or equal to 2.5 x ULN (if liver metastases are present, then less than or equal to 5 x ULN is allowed)
• Adequate renal function:
• Serum creatinine within normal limits, OR calculated creatinine clearance ≥ 60 mL/min/1.73 m2 for patients with serum creatinine above institutional ULN.
• Corrected serum calcium ≥ lower limit of the institutional normal range (LLN)
• Serum phosphorus level ≥ LLN
• Adequate hematologic function:
• Absolute Neutrophil Count ≥ 1500 cells/mm3
• Platelet count ≥ 100,000 (cells/mm3)
• Hemoglobin ≥ 9 g/dL
• Urinalysis:
• No clinically significant abnormalities
• Adequate coagulation function:
• PT ≤ 1.25 x ULN
• PTT ≤ 1.25 x ULN
• For men and women of child-producing potential, agreement to use effective contraceptive methods during the study

You may not qualify if…

• New York Heart Association Class III or IV, cardiac disease, myocardial infarction within the past 6 months, unstable arrhythmia, or evidence of ischemia on ECG
• Active, uncontrolled bacterial, viral, or fungal infections requiring systemic therapy
• Pregnant or nursing women. NOTE: Women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; or abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect that she is pregnant while participating in this study, she should inform her treating physician immediately.
• Major surgery within 4 weeks prior to Day 1, or not fully recovered by Day 1
• Minor surgery within 2 weeks prior to Day 1, or not fully recovered by Day 1
• Treatment with radiation therapy within 4 weeks prior to Day 1.
• Received systemic chemotherapy or monoclonal antibody or other immunotherapy within 4 weeks prior to Day 1 (exceptions: 6 weeks for nitrosourea, mitomycin C, or any agent with a known treatment effect > 4 weeks' duration), or not fully recovered from any side effects from previous therapy by Day 1
• History of allergic reactions attributed to excipients or chemical products used in the final GO-203-2c drug formulation
• Known infection with HIV, hepatitis B, or hepatitis C.
• Subjects with risk factors for gastrointestinal perforation or pulmonary hemorrhage (e.g. unresected luminal intestinal cancers; abdominal carcinomatosis within 3 months before the first dose of study drug, abdominal fistula, acute diverticulitis, peptic ulcer disease, irritable bowel syndrome, Crohn's disease, pulmonary hemorrhage, hemoptysis, or tuberculosis)
• Currently receiving or having received treatment with any other investigational agent within 4 weeks prior to Day 1, or not fully recovered from toxicities of prior treatment by Day 1
• Serious and/or poorly controlled non-malignant disease (including but not limited to, ongoing or active infection, hydronephrosis, hypertension, diabetes, or other conditions) that could compromise protocol objectives in the opinion of the Investigator and/or the sponsor. Patients with such conditions should be discussed with the Medical Monitor prior to enrollment. All medical conditions must be NCI CTCAE Grade 1 or lower at baseline.
• Unwillingness or inability to comply with requirements of this protocol

Where it is running

• TGen Clinical Research Service — Scottsdale, Arizona, United States
• Cedars-Sinai Medical Center — Los Angeles, California, United States
• Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
• University of Texas Health Science Center San Antonio — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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