Phase 2 Study to Investigate the Efficacy and Safety of Aldoxorubicin in Subjects With Glioblastoma

Sponsor

ImmunityBio, Inc. (Industry)

Overall Status

Completed

CT.gov ID

NCT02014844

Collaborator

(none)

Enrollment

Locations

Arm

33.1

Duration (Months)

Patients Per Site

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a pilot study to determine the efficacy and safety of aldoxorubicin in subjects with glioblastoma who have progressed following surgery and prior treatments.

Condition or Disease	Intervention/Treatment	Phase
Glioblastoma	Drug: aldoxorubicin	Phase 2

Detailed Description

This is a second line open-labeled pilot phase 2 study in subjects with glioblastoma whose tumors have progressed following prior treatment with surgery, radiation and Temozolomide. Patients who have received avastin as a second-line treatment are not eligible for this study.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

28 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

An Open-Label Pilot Phase 2 Study to Investigate the Preliminary Efficacy and Safety of Aldoxorubicin in Subjects With Unresectable Glioblastoma Whose Tumors Have Progressed Following Prior Treatment With Surgery, Radiation and Temozolomide

Study Start Date :

Mar 1, 2014

Actual Primary Completion Date :

Dec 1, 2016

Actual Study Completion Date :

Dec 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: aldoxorubicin Subjects will receive either 250 mg/m2 or 350 mg/m2 aldoxorubicin IV.	Drug: aldoxorubicin Other Names: INNO-206

Arm

Intervention/Treatment

Experimental: aldoxorubicin

Subjects will receive either 250 mg/m2 or 350 mg/m2 aldoxorubicin IV.

Drug: aldoxorubicin

Other Names:

INNO-206

Outcome Measures

Primary Outcome Measures

Objective Response Rate (Complete Response and Partial Response) [up to 6 months]
The study will measure the complete response and partial response rate in these subjects using the RANO Working Group Criteria.

Secondary Outcome Measures

Safety [up to 6 months]
The secondary objectives of this study are to evaluate the safety of aldoxorubicin in this population assessed by the frequency and severity of adverse events (AEs, abnormal findings on physical examination, laboratory tests, vital signs, echocardiogram evaluations, ECG results, weight, and the change in performance status as measured by the Karnofsky Performance Scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Age 18 years or older; male or female
Histologically or cytologically confirmed unresectable GBM. Subjects with recurrent disease whose prior pathology demonstrated GBM will not need to be re-biopsied. Subjects with prior low-grade glioma or anaplastic glioma are eligible if histological assessment demonstrates transformation into GBM.
Cancer progression after treatment with the following: surgery, radiation therapy and temozolomide as first line treatment with no other therapy prior to tumor recurrence.
Radiographic progression by RANO Working Group Criteria will be confirmed by Imaging Endpoints, a central imaging vendor.
By tumor biopsy if conducted within 4 weeks of randomization.
An interval of at least 12 weeks after last dose of radiation and temozolomide is required, unless cancer progression is proven by diagnostic tumor biopsy. If temozolomide is being used in a maintenance phase, there must be a 28-day washout period prior to Randomization.
Stable or decreasing dose of corticosteroids for at least 7 days prior to randomization.
Capable of providing informed consent and complying with trial procedures.
Karnofsky Performance Status 70 or above.
ECOG performance status 0-2.
Life expectancy 8 or more weeks.
Measurable tumor lesions according to RANO working Group Criteria.

In the case that there is "non-measurable" disease due to a radical surgical resection during screening, the subject still qualifies if Inclusion #3(b) is met.

Women must not be able to become pregnant for the duration of the study.
Women of childbearing potential must have a negative serum or urine pregnancy test at the Screening Visit and be non-lactating.
Geographically accessible to site, i.e. the ability to come to the study site for each scheduled appointment and evaluation.

Exclusion Criteria:

Prior exposure to the an anthracycline.
Any therapeutic regimen for treatment of recurrent tumor after first line treatment with surgery, radiation and temozolomide.
Prior treatment with bevacizumab or an experimental anti-angiogenic agent.
Palliative surgery and/or radiation treatment less than 4 weeks to randomization.
Exposure to any investigational agent within 30 days of Randomization.
History of other malignancies (except cured basal cell carcinoma, superficial bladder cancer or carcinoma in situ of the cervix) unless documented free of cancer for 3 or more years.
Laboratory values: screening serum creatinine > 1.5xULN, ALT > 2.5xULN, total bilirubin > 1.5xULN, ANC < 1500/mm3, platelet concentrations < 100,000/mm3, absolute lymphocyte count < 1000/mm3, hematocrit level < 27% for females or < 30% for males, serum albumin ≤ 2.5 g/dL, PT/INR 1.5xULN or >3xULN on anticoagulant with no evidence of active bleeding.
Evidence of CNS hemorrhage CTCAE ≥ grade 2 on baseline MRI.
Clinically evident congestive heart failure > class II of the NYHA guidelines.
Current, serious, clinically significant cardiac arrhythmias, defined as the existence of an absolute arrhythmia or ventricular arrythmias classified as Lown III, IV or V.
History or signs of active coronary artery disease with or without angina pectoris.
Serious myocardial dysfunction defined as ultrasound-determined LVEF < 45% of predicted institutional normal value.
Baseline ATc>470 msec and/or previous history of QT prolongation.
Active, clinically significant serious infection requiring treatment with antibiotics, anti-virals, or anti-fungals.
History of HIV infection.
Major surgery, except diagnostic tumor biopsy, within 4 weeks of randomization.
Any condition that might interfere with the subject's participation in the study or in the evaluation of the study results.
Any condition that is unstable and could jeopardize the subject's participation in the study.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	City of Hope National Medical Center	Duarte	California	United States	91010
2	Sarcoma Oncology Center	Santa Monica	California	United States	90403
3	Ochsner Health System	New Orleans	Louisiana	United States	70115-6969
4	Texas Oncology-Austin Midtown	Austin	Texas	United States	78705