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Safety and Tolerability Study of RAD001 and LBH589 in All Solid Tumors With Enrichment for EBV Driven Tumors

Primary Purpose

Nasopharyngeal Carcinoma, Lymphomas, Any EBV+ Solid Tumour

Status
Unknown status
Phase
Phase 1
Locations
Singapore
Study Type
Interventional
Intervention
LBH589 and RAD001
Sponsored by
National Cancer Centre, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Nasopharyngeal Carcinoma, Lymphomas, Any EBV+ Solid Tumour focused on measuring Nasopharyngeal carcinoma, antiangiogenesis, HDACi, mTOR, Phase Ib

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  1. Patients with histologically or cytologically confirmed solid malignancy or lymphoma that is metastatic or unresectable, and for which standard curative or palliative measures do not exist or are no longer effective.

    For enrichment and dose expansion phase only:

    Only patients with EBV-related tumors, including all nasopharyngeal carcinoma, as well as tumors known to be EBV-related which include (but are not limited to) gastric carcinoma (10-15%), lymphoma. These tumors (NPC excluded) should have:

    i)EBER in situ hybridisation on paraffin samples/ circulating tumor cells; or ii)Elevated pre-treatment serum EBV viral titres

  2. Patients who have had prior treatment with mTOR inhibitors and HDAC inhibitors will be allowed ONLY in the dose escalation phase
  3. Age ≥ 21 years old.
  4. Performance status of ≤ 2 (ECOG scale).
  5. Target lesion on spiral CT or MRI scan must have at least one diameter > 1 cm (on conventional CT scan the indicator lesion must have at least one diameter > 2 cm) (for dose expansion).
  6. Adequate bone marrow reserve: absolute granulocyte count > 1 x 109/L, hemoglobin > 8 g/dL and platelet count >100,000/dL.
  7. Adequate hepatic function (serum total bilirubin level < 1.5 x ULN; alanine transaminase (ALT) and aspartate transaminase (AST) less than 3 times ULN.
  8. Adequate renal function (creatinine < 1.5 times ULN).
  9. Normal ECG at baseline - with no significant conduction abnormalities and a QTc ≤ 450.
  10. Left Ventricular Ejection Fraction ≥ 50% as assessed by MUGA scan or echocardiography at screening.
  11. No concurrent use of investigational antineoplastic therapy.
  12. No medical problems severe enough to prevent compliance with the study requirements
  13. Negative pregnancy test (urinary β-HCG) at screening (applicable to women of child bearing potential who are sexually active).
  14. Subjects must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study.

Exclusion Criteria:

  1. Known brain metastases (locally advanced NPC with direct extension to central nervous system is permissible).
  2. Chemotherapy (in the case of nitrosoureas and mitomycin C within 6 weeks), radiotherapy, immunotherapy within 4 weeks before study drug administration.
  3. Patients receiving chronic immunosuppressive treatment with high dose corticosteroids (tailing doses or low doses are acceptable) or another immunosuppressive agent;
  4. Patients with uncontrolled diabetes (fasting glucose > 2x ULN);
  5. History of uncontrolled heart disease (unstable angina, congestive heart failure, myocardial infarction within preceding 12 months, clinically significant rhythm or conduction abnormality such as second and third degree heart block, congenital long QT syndrome, obligate use of a cardiac pacemaker. Patients with QTc at screening > 450 ms.
  6. Subjects taking medications known to have a risk of causing causing QTc prolongation and Torsades de Pointes (risk group 1 as indicated on webpage: http://www.torsades.org).
  7. Patients who will need valproic acid for any medical condition during the study or within 5 days prior to the first panobinostat treatment.
  8. Patients with impairment of GI function or GI disease that may significantly alter panobinostat absorption.
  9. Patients with unresolved diarrhea of grade 2 and above.
  10. Patients with a known history of Hepatitis B, C and HIV seropositivity.
  11. Patients with an active bleeding diathesis;
  12. Subjects with Grade ≥ 2 neuropathy at baseline.
  13. For patients undergoing magnetic resonance imaging (MRI) studies (including DCE-MRI, BOLD-MRI and DWI-MRI) in the expansion cohort:

    1. Contraindications to MRI, e.g. contraindicated metal implants
    2. Patients with poor antecubital fossa venous access.

Sites / Locations

  • National Cancer Center Singapore

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

LBH589-RAD001

Arm Description

LBH589-RAD001, single arm dose finding study

Outcomes

Primary Outcome Measures

Safety and tolerability
Patients will be followed closely for toxicities in the first cycle where they would have weekly consultations visit. After the first cycle, consultation visits will be once every 2 weeks or once a month depending on how well the patient is tolerating the treatment. The following safety assesments will be done on every visit; Vital signs and physical examination Haematology and blood chemistry Cardiac monitoring EBV DNA titre (for patients with EBV Driven tumors recording of adverse events and serious adverse events.

Secondary Outcome Measures

Tumor response
Tumor response will be evaluated at the end of every 8-weeks of treatment. Treatment will continue until one of the following occur; disease progression, unacceptable toxicity, death, or withdrawal from study. Best response (according to RECIST), as well as progression free survival will be reported.

Full Information

First Posted
April 21, 2011
Last Updated
April 22, 2018
Sponsor
National Cancer Centre, Singapore
Collaborators
Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT01341834
Brief Title
Safety and Tolerability Study of RAD001 and LBH589 in All Solid Tumors With Enrichment for EBV Driven Tumors
Official Title
A Safety and Tolerability Study of RAD001 (mTOR Inhibitor) in Combination With Two Dosing Schedules of LBH589B (Histone Deacetylase Inhibitor) in Solid Tumors/ Lymphomas With Enrichment for EBV-Driven Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 2010 (Actual)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Cancer Centre, Singapore
Collaborators
Novartis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is: To determine the optimal recommended phase II dose of two investigational study drugs, LBH589 and RAD001, given in combination in all solid tumors (With enrichment for EBV-Driven tumors). To determine the pharmacokinetic profile of RAD001 in combination with two schedules of LBH589. To assess the preliminary anti-tumor activity of RAD001 and LBH589. This study will also be exploring the hypothesis that HDACi and mTOR inhibitors abrogate the effects of key viral proteins, and switch the virus from a latent proliferative phase to a lytic phase. Immunologic correlates will also be examined to ascertain T-cell subpopulations and expression of HLA class molecules. DCE-MRI will be subsequently employed in dose expansion to examine antiangiogenic effects.
Detailed Description
Dose escalation phase 1B of the study will evaluate the safety and tolerability of RAD001 in combination with LBH589 in all solid tumors, lymphomas; and enriched for EBV driven tumors. The phase 2 component will be a single arm, non-randomized study restricted to nasopharyngeal carinoma only (endemic type). A "3+3" dose escalation design will be adopted. Patients will start taking LBH589 three times a week and will have a run in period of one week, followed by continous administration of RAD001 from week 2. Pharmacokinetic assessments will be done on day 1 of LBH589 administration and day 1 of concurrent administration of LBH589 + RAD001. ON day 31, there will be a one week drug holiday. This is done to explore the eliminaition kinetics from steady state,as well as the durability of target modulation. AEs of patients will be monitored closely. In the event of grade 3/4 toxicity, the cohort will be expanded to 6. Dose escalation of LBH589/RAD001 may proceed until the maximum tolerated dose (MTD)is reached. Once the MTD is established, an expasion cohort comprising 20 EBV driven tumors will open at two different LBH589 dose schedules. Treatment will be continued until progression of disease, unacceptable toxcity, or discontinuation criterion is met.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nasopharyngeal Carcinoma, Lymphomas, Any EBV+ Solid Tumour
Keywords
Nasopharyngeal carcinoma, antiangiogenesis, HDACi, mTOR, Phase Ib

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
49 (Actual)

8. Arms, Groups, and Interventions

Arm Title
LBH589-RAD001
Arm Type
Experimental
Arm Description
LBH589-RAD001, single arm dose finding study
Intervention Type
Drug
Intervention Name(s)
LBH589 and RAD001
Intervention Description
Dose escalation of LBH589 tablets (5 and 10 mg) and RAD001 tablets (2.5, 5 mg and 10mg)
Primary Outcome Measure Information:
Title
Safety and tolerability
Description
Patients will be followed closely for toxicities in the first cycle where they would have weekly consultations visit. After the first cycle, consultation visits will be once every 2 weeks or once a month depending on how well the patient is tolerating the treatment. The following safety assesments will be done on every visit; Vital signs and physical examination Haematology and blood chemistry Cardiac monitoring EBV DNA titre (for patients with EBV Driven tumors recording of adverse events and serious adverse events.
Time Frame
Weekly evaluation for the first 5 weeks (DLT period), and continued follow up until patients come off trial due to toxicity or progressive disease
Secondary Outcome Measure Information:
Title
Tumor response
Description
Tumor response will be evaluated at the end of every 8-weeks of treatment. Treatment will continue until one of the following occur; disease progression, unacceptable toxicity, death, or withdrawal from study. Best response (according to RECIST), as well as progression free survival will be reported.
Time Frame
Every 2 months until disease progression or withdrawal from study - average of 6 - 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Patients with histologically or cytologically confirmed solid malignancy or lymphoma that is metastatic or unresectable, and for which standard curative or palliative measures do not exist or are no longer effective. For enrichment and dose expansion phase only: Only patients with EBV-related tumors, including all nasopharyngeal carcinoma, as well as tumors known to be EBV-related which include (but are not limited to) gastric carcinoma (10-15%), lymphoma. These tumors (NPC excluded) should have: i)EBER in situ hybridisation on paraffin samples/ circulating tumor cells; or ii)Elevated pre-treatment serum EBV viral titres Patients who have had prior treatment with mTOR inhibitors and HDAC inhibitors will be allowed ONLY in the dose escalation phase Age ≥ 21 years old. Performance status of ≤ 2 (ECOG scale). Target lesion on spiral CT or MRI scan must have at least one diameter > 1 cm (on conventional CT scan the indicator lesion must have at least one diameter > 2 cm) (for dose expansion). Adequate bone marrow reserve: absolute granulocyte count > 1 x 109/L, hemoglobin > 8 g/dL and platelet count >100,000/dL. Adequate hepatic function (serum total bilirubin level < 1.5 x ULN; alanine transaminase (ALT) and aspartate transaminase (AST) less than 3 times ULN. Adequate renal function (creatinine < 1.5 times ULN). Normal ECG at baseline - with no significant conduction abnormalities and a QTc ≤ 450. Left Ventricular Ejection Fraction ≥ 50% as assessed by MUGA scan or echocardiography at screening. No concurrent use of investigational antineoplastic therapy. No medical problems severe enough to prevent compliance with the study requirements Negative pregnancy test (urinary β-HCG) at screening (applicable to women of child bearing potential who are sexually active). Subjects must have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study. Exclusion Criteria: Known brain metastases (locally advanced NPC with direct extension to central nervous system is permissible). Chemotherapy (in the case of nitrosoureas and mitomycin C within 6 weeks), radiotherapy, immunotherapy within 4 weeks before study drug administration. Patients receiving chronic immunosuppressive treatment with high dose corticosteroids (tailing doses or low doses are acceptable) or another immunosuppressive agent; Patients with uncontrolled diabetes (fasting glucose > 2x ULN); History of uncontrolled heart disease (unstable angina, congestive heart failure, myocardial infarction within preceding 12 months, clinically significant rhythm or conduction abnormality such as second and third degree heart block, congenital long QT syndrome, obligate use of a cardiac pacemaker. Patients with QTc at screening > 450 ms. Subjects taking medications known to have a risk of causing causing QTc prolongation and Torsades de Pointes (risk group 1 as indicated on webpage: http://www.torsades.org). Patients who will need valproic acid for any medical condition during the study or within 5 days prior to the first panobinostat treatment. Patients with impairment of GI function or GI disease that may significantly alter panobinostat absorption. Patients with unresolved diarrhea of grade 2 and above. Patients with a known history of Hepatitis B, C and HIV seropositivity. Patients with an active bleeding diathesis; Subjects with Grade ≥ 2 neuropathy at baseline. For patients undergoing magnetic resonance imaging (MRI) studies (including DCE-MRI, BOLD-MRI and DWI-MRI) in the expansion cohort: Contraindications to MRI, e.g. contraindicated metal implants Patients with poor antecubital fossa venous access.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel Tan Shao Weng
Organizational Affiliation
National Cancer Center Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Cancer Center Singapore
City
Singapore
ZIP/Postal Code
169690
Country
Singapore

12. IPD Sharing Statement

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Safety and Tolerability Study of RAD001 and LBH589 in All Solid Tumors With Enrichment for EBV Driven Tumors

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