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Study of VAL-083 in Patients With MGMT Unmethylated, Bevacizumab-naive Recurrent Glioblastoma

This study is currently recruiting participants.
Verified October 2017 by DelMar Pharmaceuticals, Inc.
Sponsor:
ClinicalTrials.gov Identifier:
NCT02717962
First Posted: March 24, 2016
Last Update Posted: October 20, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
DelMar Pharmaceuticals, Inc.
March 16, 2016
March 24, 2016
October 20, 2017
January 20, 2017
September 2020   (Final data collection date for primary outcome measure)
Overall Survival [ Time Frame: Every 30 days from randomization until patient death or for at least 9 months, whichever occurs earlier ]
Length of time from start of treatment (Day 1) until patient death
Overall Survival [ Time Frame: 9 months ]
Complete list of historical versions of study NCT02717962 on ClinicalTrials.gov Archive Site
  • Estimate Progression-free Survival [ Time Frame: Every 30 days from randomization until disease progression or patient death, whichever occurs earlier, for at least 9 months ]
    Time from start of treatment (Day 1) until to the first occurrence of progression or patient death, whichever occurs first
  • Estimate Median Progression-Free Survival [ Time Frame: Every 30 days from randomization until disease progression or patient death, whichever occurs earlier, for at least 9 months ]
    The median length of time from start of treatment (Day 1) until to the first occurrence of progression or patient death, whichever occurs first
  • Estimate Median Overall Survival [ Time Frame: Every 30 days from randomization until patient death or for at least 9 months, whichever occurs earlier ]
    The median length of time from start of treatment (Day 1) until patient death
  • Estimate Overall Response Rate [ Time Frame: Every 42 days from randomization to achievement of either complete response (CR) or partial response (PR) for at least 9 months ]
    Overall number of tumor complete response (CR) or partial response (PR) determined via MRI assessment
  • Estimate Duration of Response [ Time Frame: Every 42 days from the first occurrence of a documented, objective response until the time of relapse or patient death, for at least 9 months, whichever occurs earlier ]
    Length of time tumor continues to demonstrate either complete response (CR) or partial response (PR) via MRI assessment
  • Safety evaluation of VAL-083 in patients [ Time Frame: From randomization up to 28 days following last study treatment ]
    To confirm safety and tolerability of VAL-083 using NCI CTCAE v.4 to assess adverse events
  • Quality of Life [ Time Frame: Every 42 days from randomization until disease progression, for at least 9 months ]
    MD Anderson Symptom Inventory-Brain Tumor Module (MDASI-BT)
  • Plasma Pharmacokinetics [ Time Frame: Cycle 1 Day 1 predose, 15 ± 5 min, 30 ± 5 min, 60 ± 10 min, 120 ± 10 min, 240 ± 15 min, and 360 ± 15 min after the end of the of iv infusion of VAL-083 ]
    PK profile and dose-exposure relationship of VAL-083
  • Progression-free Survival [ Time Frame: 6 months ]
  • Median Progression-Free Survival [ Time Frame: From randomization until progression or death, whichever occurs first, assessed up to 9 months ]
  • Median Overall Survival [ Time Frame: From randomization to death from any cause, assessed up to 9 months ]
  • Overall Response Rate [ Time Frame: From randomization to achievement of either complete response (CR) or partial response (PR), assessed up to 9 months ]
  • Duration of Response Rate [ Time Frame: From the first occurrence of a documented, objective response until the time of relapse or death from any cause, assessed up to 9 months ]
  • Number of participants with treatment-related adverse events assessed using NCI CTCAE v.4 [ Time Frame: assessed up to 9 months ]
  • Quality of Life [ Time Frame: assessed up to 9 months ]
    MD Anderson Symptom Inventory-Brain Tumor Module (MDASI-BT)
Not Provided
Not Provided
 
Study of VAL-083 in Patients With MGMT Unmethylated, Bevacizumab-naive Recurrent Glioblastoma
Phase II Study of VAL-083 in Patients With MGMT Unmethylated, Bevacizumab-naive Recurrent Glioblastoma
The purpose of this phase 2, single arm, biomarker-driven study is to determine if treatment of O-6-methylguanine-DNA methyltransferase (MGMT) unmethylated recurrent glioblastoma with VAL-083 improves overall survival (OS), compared to historical control.

Recurrent glioblastoma (GBM) is characterized by a dismal prognosis, with a median overall survival of 6-9 months. While a standard of care is established for the initial treatment of GBM - radiation with concurrent and adjuvant temozolomide chemotherapy - management of recurrent disease remains suboptimal. Treatment options include repeat surgery, re-irradiation, or chemotherapy (including experimental targeted therapies, biologic agents, and immunotherapies). Only a minority of patients has response to these treatments, and the resultant benefits in progression-free and overall survival are on the order of weeks to months.

Prognosis and response to therapy are known to be better in patients with a methylated MGMT promoter gene. Epigenetic silencing of MGMT by promoter methylation is an important factor in predicting outcome for patients with GBM treated with temozolomide. Approximately 66% of GBM tumors are MGMT unmethylated (high expression of MGMT), which through a MGMT repair mechanism, confers resistance to temozolomide, the standard chemotherapy treatment of GBM.

VAL-083, Dianhydrogalactitol (DAG), unlike temozolomide, is demonstrated to be active independent of MGMT resistance mechanisms, in vitro. Thus, it may provide a treatment option for those patients that are considered likely to be poor responders to temozolomide.

This is a non-comparative, single arm, biomarker-driven study with VAL-083. Forty-eight (48) eligible patients will receive VAL-083 at 40 mg/m2 IV on days 1, 2, and 3, for up to 12, 21-day treatment cycles or until they fulfill one of the criteria for study discontinuation (disease progression, death, intolerable toxicities, investigator's judgment, or withdrawal of consent). Disease status will be evaluated with clinical and MRI evaluation every other 21-day cycle, while the patient is receiving VAL-083 treatment, and then approximately every 42 ± 7 days while remaining on study. Symptom burden will be evaluated using the MD Anderson Symptom Inventory-Brain Tumor (MDASI-BT) completed by patients at baseline and at the time of each imaging evaluation.

Interval medical histories, targeted physical exams, neurologic evaluations, complete blood counts, and other laboratory and safety assessments will be performed approximately every 21-days. Blood samples will be taken at Cycle 1 Day 1 pre-dose, 15 ± 5 min, 30 ± 5 min, 60 ± 10 min, 120 ± 10 min, 240 ± 15 min, and 360 ± 15 min after the end of the of iv infusion with VAL-083 to determine the PK profile and dose-exposure relationship of VAL-083.

Toxicity will be evaluated and documented using the NCI CTCAE version 4.

This study will take approximately 32 months to enroll.

Interventional
Phase 2
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Glioma
  • Glioblastoma
  • Glioblastoma Multiforme
  • GBM
  • Brain Cancer
Drug: VAL-083, Dianhydrogalactitol
The dosing regimen for patients will be VAL-083 (40 mg/m2) administered IV for 3 consecutive days at the beginning of every 21-day cycle. Patients will continue to receive VAL 083, for up to 12, 21-day treatment cycles or until they fulfill one of the criteria for study discontinuation.
Experimental: VAL-083, Dianhydrogalactitol
VAL-083 at 40 mg/m2 IV on days 1, 2, and 3 of a 21-day treatment-cycle, for up to 12, 21-day treatment cycles or until they fulfill one of the criteria for study discontinuation. VAL-083 will be administered as an IV infusion over 30-60 minutes.
Intervention: Drug: VAL-083, Dianhydrogalactitol
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
48
June 2021
September 2020   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patient must willingly provide written consent after being informed of the procedure to be followed, the experimental nature of the therapy, alternatives, potential benefits, side effects, risks, and discomforts.
  • Patients must be ≥ 18 years old.
  • Patients must have histologically confirmed initial diagnosis of primary intracranial World Health Organization (WHO) Grade IV malignant glioma (glioblastoma, GBM), now recurrent. Patients with recurrent disease whose initial diagnostic pathology confirmed glioblastoma will not need re-biopsy. Alternately, patients with prior intracranial low-grade glioma or anaplastic glioma will be eligible, if histologic assessment demonstrates transformation to GBM (first diagnosis of secondary GBM).
  • Patients must have radiographic evidence of recurrent/progressive GBM after prior therapy (biopsy or resection and chemoradiation); 1st recurrence of GBM only, per Response Assessment in Neuro-Oncology Criteria (RANO) criteria. Histologically documented transformation from a lower grade gliomas will be considered first recurrence.
  • Patients must have confirmed GBM MGMT status (tumor must be MGMT promoter unmethylated) by central laboratory Clinical Laboratory Improvement Amendments (CLIA) certified testing at MD Anderson, prior to registration. If initial MGMT testing obtained at an outside institution, MGMT status must be centrally retested at MD Anderson.
  • Patients must have Karnofsky Performance Status (KPS) > 60% (i.e., 70, 80, 90 or 100).
  • Patients must have been previously treated for GBM with radiation with concurrent and adjuvant temozolomide chemotherapy.
  • Adequate recovery from all recent surgery is required. At least 21-days must have elapsed from the time of any major surgery, including craniotomy/tumor resection. Patients must have recovered from all surgery-related toxicities to Grade 1 or less.
  • Patients must ≥ 12 weeks from radiotherapy, to minimize the potential for magnetic resonance imaging (MRI) changes related to treatment (pseudo progression) that might be misdiagnosed as true progression of disease, unless the patient fulfills criteria for early progressive disease by RANO.
  • Prior therapy with gamma knife or other focal high-dose radiation is allowed, but at least 2 weeks must have elapsed from the time of treatment, and the patient must have subsequent histologic documentation of recurrence, unless the recurrence is a new lesion outside the irradiated field.
  • Patients having prior therapy with Laser Induced Thermal Therapy (LITT) is allowed, but at least 21 days must have elapsed from last LITT, with recovery from all LITT-related toxicities to Grade 1 or less and subsequent histologic documentation of recurrence
  • Patients must be at least 4 weeks from last dose of chemotherapy.
  • Patients must be at least 4 weeks or 5 half-lives (whichever is shorter) from the last dose of prior investigational anti-cancer drugs.
  • Patients must have recovered from all treatment-related toxicities to Grade 1 or less.
  • If receiving corticosteroids, patients must be on a stable or decreasing dose of corticosteroids for ≥ 5 days prior to baseline MRI.
  • Patients must have a predicted life expectancy of at least 12 weeks.
  • Patients must have adequate bone marrow and organ function.
  • Patients must be willing and able to comply with scheduled visits, treatment plan, and laboratory tests and accessible for follow-up.
  • If the patient has been using the Optune™ device, it will be discontinued before initiating treatment with either study medication, and per inclusion criterion listed above, the patient must have recovered from all treatment-related toxicities to Grade 1 or less.
  • Pregnancy restrictions - Women of childbearing potential must have a negative B-HCG documented within 7 days prior to registration

Exclusion Criteria:

  • Within 12 weeks of chemoradiation unless the patient fulfills criteria for early progressive disease by RANO
  • Receipt of investigational agents within 5 half-lives of last dose of investigational agent
  • Concurrent use of other investigational agents or Optune™ device
  • Prior therapy with lomustine
  • Prior therapy with bevacizumab
  • Current history of neoplasm other than the entry diagnosis. Patients with previous cancers treated and cured with local therapy alone may be considered with approval of the PI
  • Evidence of leptomeningeal spread of disease
  • Need for urgent palliative intervention (e.g., impending herniation)
  • Severe, intercurrent illness including, but not limited to unstable systemic disease, including ongoing or active infection, uncontrolled hypertension, serious cardiac arrhythmia requiring medication, or psychiatric illness/social situations that would limit compliance with study requirements
  • Patients with a known sensitivity to any of the products to be administered during treatment
  • Patients unable to undergo MRI of the brain
  • Women who are pregnant or lactating. Women of childbearing potential must have a negative serum or urine pregnancy test performed within 7 days prior to start of treatment. Women of childbearing potential or men with partners of childbearing potential must use effective birth control measures during treatment.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact: Lorena Lopez, B.S. 925-292-8360 llopez@solsentinel.com
Contact: John Langlands, Ph.D. 604-629-5989 jlanglands@delmarpharma.com
United States
 
 
NCT02717962
DLM-16-001
No
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Plan to Share IPD: No
Plan Description: The Clinical Study Report for this trial will be prepared and provided to U.S. F.D.A. as required by applicable regulatory requirement(s). Each participating trial investigator will be provided a copy their patient data captured in the electronic data base for this trial.
DelMar Pharmaceuticals, Inc.
DelMar Pharmaceuticals, Inc.
Not Provided
Principal Investigator: Barbara O'Brien, M.D. University of Texas, MDAnderson Cancer Center, Houston, Texas, USA 77030
DelMar Pharmaceuticals, Inc.
October 2017

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