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Study of the Glutaminase Inhibitor CB-839 in Solid Tumors

Brief Summary

Many tumor cells, in contrast to normal cells, have been shown to require the amino acid glutamine to produce energy for growth and survival. To exploit the dependence of tumors on glutamine, CB-839, a potent and selective inhibitor of the first enzyme in glutamine utilization, glutaminase, will be tested in this Phase 1 study in patients with solid tumors.

This study is an open-label Phase 1 evaluation of CB-839 in patients with advanced solid tumors. The study will be conducted in 2 parts. Part 1 is a dose escalation study enrolling patients with locally-advanced, metastatic and/or refractory solid tumors to receive CB-839 capsules orally twice or three times daily.

In Part 2, patients with each of the following diseases will be enrolled: A) Triple-Negative Breast Cancer, B) Non-Small Cell Lung Cancer (adenocarcinoma), C) Renal Cell Cancer, D) Mesothelioma, E) Fumarate hydratase (FH)-deficient tumors, F) Succinate dehydrogenase (SDH)-deficient gastrointestinal stromal tumors (GIST), G) SDH-deficient non-GIST tumors, H) tumors harboring mutations in isocitrate dehydrogenase-1 (IDH1) or IDH2, and I) cMyc mutation tumors.

As an extension of Parts 1 & 2, patients will be treated with CB-839 in combination with standard chemotherapy. Combination groups include: Pac-CB, CBE, CB-Erl, CBD, and CB-Cabo. Pac-CB: patients with locally-advanced or metastatic TNBC will be treated with paclitaxel and CB-839. CBE: patients with advanced clear cell RCC or papillary RCC will be treated with everolimus in combination with CB-839. CB-Erl: patients with advanced NSCLC lacking the T790M EGFR mutation will be treated with erlotinib and CB-839. CBD: patients with NSCLC harboring KRAS mutation will be treated with docetaxel and CB-839. CB-Cabo: patients with histologically confirmed diagnosis of locally-advanced, inoperable or metastatic RCC treated with cabozantinib in combination with CB-839.

All patients will be assessed for safety, pharmacokinetics (plasma concentration of drug), pharmacodynamics (inhibition of glutaminase), biomarkers (biochemical markers that may predict responsiveness in later studies), and tumor response.

Tracking Information
First Received DateFebruary 14, 2014
Last Changed DateAugust 18, 2016
Start DateFebruary 2014
Anticipated Primary Completion DateJune 2017
Primary Outcome Measures

Safety and tolerability of CB-839: Incidence of adverse events [Time Frame: Every 21 days from study start until disease progression or unacceptable toxicity, assessed for an expected average of 6 months]

Secondary Outcome Measures

Pharmacokinetics: Area under the Curve (AUC) of CB-839 concentration in blood [Time Frame: Study Days 1, 15, and 22]

Pharmacodynamics: % inhibition of glutaminase in blood [Time Frame: Study Days 1 and 15]

Clinical activity: Change in tumor volume from baseline [Time Frame: Every 9 weeks until disease progression or unacceptable toxicity, assessed for an expected average of 6 months]

Descriptive Information
PhasePhase 1
Study TypeInterventional
Condition
  • Solid Tumors
  • Triple-Negative Breast Cancer
  • Non Small Cell Lung Cancer
  • Renal Cell Carcinoma
  • Mesothelioma
  • Fumarate Hydratase (FH)-Deficient Tumors
  • Succinate Dehydrogenase (SDH)-Deficient Gastrointestinal Stromal Tumors (GIST)
  • Succinate Dehydrogenase (SDH)-Deficient Non-gastrointestinal Stromal Tumors
  • Tumors Harboring Isocitrate Dehydrogenase-1 (IDH1) and IDH2 Mutations
  • Tumors Harboring Amplifications in the cMyc Gene
Intervention
  • Drug: CB-839
  • Drug: Pac-CB
  • Drug: CBE
  • Drug: CB-Erl
  • Drug: CBD
  • Drug: CB-Cabo
Study Arms / Comparison Groups6 / 0
Recruitment Information
Recruitment StatusRecruiting
Anticipated Enrollment205
GenderAll
Ages18 Years - N/A
Accepts Healthy VolunteersNo
Contact Clinical Administrator
Email: clinicaltrials@calithera.com
Eligibility Criteria

Inclusion criteria

- Advanced malignancy that is relapsed and/or refractory to all available therapies that will confer clinical benefit. Newly diagnosed patients who refuse standard treatment regimens are also eligible

- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1

- Life Expectancy of at least 3 months

- Adequate hepatic, renal, cardiac, and hematologic function

- Measurable disease by RECIST criteria

- Ability to provide written informed consent in accordance with federal, local, and institutional guidelines

Exclusion Criteria

- Any other current or previous malignancy

- Chemotherapy, radiation therapy, hormonal therapy, immunotherapy or biological therapy, or investigational agent within 21 days

- Unable to receive medications oral medications

- Major surgery within 28 days before Cycle 1 Day 1

- Active infection requiring within 2 weeks prior to first dose of study drug

- Patients who have HIV, Hepatitis A, B or C or CMV reactivation

- Significant neurotoxicity/neuropathy (Grade 3 or higher) within 14 days of first dose of study drug

- Conditions that could interfere with treatment or protocol-related procedures

Administrative Information
NCTIDNCT02071862
Responsible Party,
SponsorCalithera Biosciences, Inc
Verification DateAugust 2016
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