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A Study to Investigate the Safety and Efficacy of AT13387, Alone or in Combination With Imatinib, in Patients With GIST

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Astex Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT01294202
First received: February 10, 2011
Last updated: May 6, 2014
Last verified: April 2014

February 10, 2011
May 6, 2014
March 2011
May 2014   (final data collection date for primary outcome measure)
Rate of reduction/stabilisation of tumour size at 4 months according to Response Evaluation Criteria In Solid Tumors (RECIST) version 1.1 criteria [ Time Frame: 4 months ] [ Designated as safety issue: No ]
Rate of reduction/stabilisation of tumour size at 4 months according to RECIST version 1.1 criteria [ Time Frame: 4 months ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT01294202 on ClinicalTrials.gov Archive Site
  • Rate of reduction/stabilisation of tumour size at 6 months (6-month 'disease control rate' [DCR]), determined according to RECIST version 1.1 criteria. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Progression-free survival at 6 months, and estimated proportion of patients surviving at 6 months. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Objective responses, using RECIST version 1.1 criteria [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Changes in pharmacodynamic biomarkers assessed in tumour biopsies and plasma samples, and changes in tumour metabolism by Fludeoxyglucose - Positron emission tomography scans (FDG-PET). [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Relationships between KIT and PDGRFA tumour mutational status, changes in tumour dimensions, and exploratory pharmacodynamic biomarkers. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Pharmacokinetic profile of AT13387 given in combination with imatinib. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Treatment emergent adverse events, classified by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 4.03. [ Time Frame: 6 months ] [ Designated as safety issue: Yes ]
  • Rate of reduction/stabilisation of tumour size at 6 months (6-month 'disease control rate' [DCR]), determined according to RECIST version 1.1 criteria. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Progression-free survival at 6 months, and estimated proportion of patients surviving at 6 months. [ Time Frame: 6 months ] [ Designated as safety issue: No ]
  • Objective responses, using RECIST version 1.1 criteria [ Designated as safety issue: No ]
  • Changes in pharmacodynamic biomarkers assessed in tumour biopsies and plasma samples, and changes in tumour metabolism by FDG-PET scans [ Designated as safety issue: No ]
  • Relationships between KIT and PDGRFA tumour mutational status, changes in tumour dimensions, and exploratory pharmacodynamic biomarkers. [ Designated as safety issue: No ]
  • Pharmacokinetic profile of AT13387 given in combination with imatinib. [ Designated as safety issue: No ]
  • Treatment emergent adverse events, classified by NCI CTCAE version 4.03. [ Designated as safety issue: Yes ]
Not Provided
Not Provided
 
A Study to Investigate the Safety and Efficacy of AT13387, Alone or in Combination With Imatinib, in Patients With GIST
An Open-Label, Randomised, Multi-Centre, Phase II Study to Investigate the Safety and Efficacy of AT13387, Either as Monotherapy or in Combination With Imatinib, in Patients With Unresectable and/or Metastatic Malignant GIST Whose Tumour Has Progressed Following Treatment With a Maximum of Three Tyrosine Kinase Inhibitors

The purpose of this study is to investigate if an investigational drug called AT13387 is active against Gastrointestinal Stromal Tumor (GIST) that is resistant to other treatments, and to understand more about the safety of AT13387.

Most subjects in the study will receive AT13387 along with another drug called imatinib (Gleevec). Imatinib is a standard (approved) drug for treating patients with GIST. Some patients may receive AT13387 on its own. As a result, we shall begin to understand the effects of AT13387 given on its own and when combined with imatinib.We shall also find out more about the side-effects of AT13387, and more about how the body breaks down (metabolizes) AT13387.

The study consists of 3 parts: Part 1 is a dose escalation phase, Part 2 is a dose expansion phase and Part 3 is either a further dose expansion phase or a randomised phase in which half the patients receive AT13387 monotherapy and half continue to receive AT13387 in combination with imatinib.

All patients will receive AT13387 given by intravenous infusion on Days 1, 8, and 15 of a 28-day cycle. Most patients will also receive imatinib 400 mg by mouth every day.

Patients will have tumour imaging at baseline, and at 2, 4 and 6 months, and then at 2 month intervals until cycle 12, and then 3-monthly thereafter.

Blood samples will be taken to measure plasma drug levels of AT13387 given in combination with imatinib

Interventional
Phase 2
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Gastrointestinal Stromal Tumor (GIST)
Drug: AT13387 and Imatinib

In part 1 pts will receive AT13387 in combination with imatinib. Up to 5 possible dose levels of AT13387 could be evaluated in combination with imatinib 400 mg daily: 120 mg/m2, 150 mg/m2, 180 mg/m2, 220 mg/m2 and 260 mg/m2. AT13387 IV (in the vein) on day 1, 8 and 15 of each 28 day cycle, until progression or unacceptable toxicity develops, in order to establish the recommended phase II combination dose, which will be used in part 2 and/or part 3 of the study.

In part 2 an additional 6-9pts will be treated.

In part 3, provided that sufficient evidence of anti-tumour effect was observed in part 2 (disease stabilisation or reduction in tumour dimensions by RECIST), then an additional 12pts will be treated with AT13387 in combination with imatinib. Alternatively, if combination treatment is found to have excellent efficacy the randomised phase of the study may start so that 12 pts receive AT13387 on its own (monotherapy) and 12 pts receive AT13387 in combination with imatinib.

Other Name: Gleevec
Experimental: AT13387 and imatinib
AT13387 administered on days 1, 8 and 15, imatinib administered daily
Intervention: Drug: AT13387 and Imatinib
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
36
August 2014
May 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Ability to understand the risks of the study and to provide signed and dated informed consent and authorization to use protected health information (in accordance with national and local subject privacy regulations).
  • Age 18 years or older.
  • Unresectable and/or metastatic malignant GIST with objective progression of disease following treatment with a maximum of 3 tyrosine kinase inhibitors (TKIs) including imatinib. To clarify, it is the number of TKIs - up to a maximum of three agents, including imatinib - that is the criterion for entry, not the number of prior courses of TKI treatment.
  • Measurable disease.
  • ECOG performance status 0 or 1.
  • Negative blood or urine pregnancy test (within 7 days prior to commencing treatment), or documented evidence of surgical sterility, or natural or treatment-induced post-menopausal status with last menses >1 year ago.
  • Willing to provide a tissue block or unstained slides of archived tumour for central pathology review and genotyping, or a full pathology report and results of genotyping of a previous tumour sample, or willing to undergo a new tumour biopsy for central pathology review and genotyping during the screening period of the study (prior to dosing)

Exclusion Criteria:

  • Pregnancy or lactation (women of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to commencing treatment ). Male and female patients of childbearing potential must use appropriate birth control (abstinence, barrier methods, oral contraceptives and/or intrauterine devices) during the entire duration of the study, or the patient must be surgically sterile (with documentation in the patient's medical records).
  • Impaired liver function, as evidenced by prior liver segmentectomy or hemi-hepatectomy; or alanine or aspartate aminotransferase (ALAT/ASAT) >2.5x ULN; or alkaline phosphatase >2.0x ULN; or bilirubin >2.0x ULN.
  • Abnormal clotting, as evidenced by PT or PTT >1.5x ULN, or therapeutic/prophylactic anticoagulation.
  • Renal impairment, defined as either serum creatinine higher than the institution ULN,or estimated creatinine clearance lower than LLN (i.e. patients should have both normal serum creatinine, and normal estimated creatinine clearance)
  • Impaired marrow function, defined as haemoglobin <9.0 g/dL, neutrophils <1.5 x10^9/L, or platelets <100 x10^9/L. Patients may receive a blood transfusion for anaemia to allow entry to the study but should not be transfusion-dependent.
  • Left ventricular ejection fraction <50% on echocardiography or MUGA scan.
  • Known metastases of the central nervous system.
  • Prior anticancer therapies including tyrosine kinase inhibitors (other than imatinib) not completed within 2 weeks or 5 half-lives of the agent (including known active metabolites) prior to treatment with study drug. Patients receiving imatinib should continue to receive imatinib (400 mg daily) throughout the screening period.
  • Clinically important intolerance or safety concerns with prior use of imatinib 400 mg daily.
  • Prior treatment with an HSP90 inhibitor.
  • Major surgery within 14 days prior to treatment with study drug, or failure to recover from the effects of such surgery.
  • Wide field radiotherapy within 4 weeks prior to treatment with study drug, limited field radiation within 2 weeks, or failure to recover from such therapies.
  • History of an ischaemic cardiac event or unstable cardiac disease within 3 months of study entry.
  • QTc >450 ms using Fredericia's correction.
  • Previous malignancy, except for basal cell and squamous cell skin carcinomas or carcinoma of the uterine cervix, unless treated with curative intent more than 2 years prior to study entry.
  • Evidence of severe or uncontrolled systemic medical conditions which make it undesirable for the patient to take part in the study, or which could jeopardize protocol compliance. Patients with multiple comorbidities and/or requiring multiple concomitant medications (especially conditions/medications which may impair renal function or predispose to renal impairment) should be discussed with the Astex Medical Monitor at the discretion of the Investigator before enrollment.
  • Prior history of infection with HIV, or known active hepatitis B or C viral infection (active screening for viral infections is not required for study entry).
  • Significant visual impairment such that in the opinion of the investigator, further minor deterioration would have unacceptable consequences (eg. loss of ability to drive or live at home.
  • The Safety Monitoring Committee may add other specific exclusion criteria to enhance the safety of the patients based on emerging safety data.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01294202
AT13387/0002
No
Astex Pharmaceuticals
Astex Pharmaceuticals
Not Provided
Principal Investigator: George D Demetri, MD Dana-Farber Cancer Institute
Astex Pharmaceuticals
April 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP