A Phase 1 Trial of CBL0137 in Patients With Metastatic or Unresectable Advanced Solid Neoplasm

Completed · Phase 1

Conditions studied: Solid Tumors, Glioblastoma

In brief

This is an open-label, multi-center, sequential groups, dose-escalation study of CBL0137 administered intravenously in participants with metastatic or unresectable advanced solid malignancies.

Key facts

Study ID

NCT01905228

Run by

Incuron

People needed

83

Starts

2013-07-01

Expected to finish

2019-06-01

Last updated by the study team

2020-12-10

Who can join

Age: 15 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients must have histological or cytological evidence of a solid neoplasm
• Patients enrolled in the expansion cohort must have at least one measureable lesion as defined by the RECIST 1.1 criteria for patients with systemic tumors or the RANO criteria for patients with gliomas;
• Patients with a systemic tumor must:
• have metastatic or unresectable advanced solid tumors that have recurred or progressed following standard therapy or
• no longer be candidates for standard therapy or
• have tumors for which there is no standard therapy
• Patients with a glioma must:
• have Grade III (anaplastic astrocytoma, anaplastic oligodendroglioma, anaplastic oligoastrocytoma) disease, Grade IV (glioblastoma) disease, or diffuse intrinsic pontine glioma (DIPG) and;
• have received prior therapy including radiation and drug therapy and;
• have documented recurrent disease as defined in the RANO criteria;
• Patients must be ambulatory and have an ECOG Performance Score of 0 or 1;
• Patients or their legal representative must be able to provide written informed consent;
• Patients must have adequate bone marrow reserve as evidenced by:
• White Blood Cell Count (WBC) > 3,000/µL
• Absolute Neutrophil Count (ANC) > 1,500/µL
• Platelet count (PLT) > 75,000/µL
• Hemoglobin (HGB) > 8.0 gm/dL (patients may be transfused to achieve this HGB level);
• Patients must have adequate hepatic function as evidenced by:
• Serum AST/ALT < 3X the upper limit of normal (ULN) for the reference lab (< 5X the ULN for patients with known hepatic metastases)
• Serum bilirubin < 1.5 x the ULN for the reference lab;

You may not qualify if…

• Patients with active infection or with a fever > 38.50 C within 3 days of the first scheduled day of dosing;
• Patients with symptomatic CNS metastases who have not undergone surgery and/or radiotherapy and/or who are not neurologically stable;
• Patients with known hypersensitivity to any of the components of CBL0137;
• Patients who are receiving concurrent anticancer therapy;
• Patients receiving enzyme-inducing antiepileptic agents within 14 days prior to the start of study therapy;
• Males with mean QTcF values of > 450 msec and females with QTcF values of > 470 msec following 3 ECGs conducted 5 minutes apart from each other; patients who are known to have congenital prolonged QT syndromes; or patients who are on medications known to cause prolonged QT intervals on ECG;
• Please speak with the PI for the complete Inclusion/Exclusion listing.

Where it is running

• Roswell Park Cancer Institute — Buffalo, New York, United States
• University Hospital of Cleveland — Cleveland, Ohio, United States
• Cleveland Clinic — Cleveland, Ohio, United States
• CTRC at The University of Texas Healh Science Center at San Antonio — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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