Glioblastoma Multiforme Clinical Trial
Official title:
BrUOG 263: PSMA ADC for Recurrent Glioblastoma Multiforme (GBM): A Phase II Brown University Oncology Research Group Study
NCT number | NCT01856933 |
Other study ID # | 263 |
Secondary ID | |
Status | Completed |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | May 2013 |
Est. completion date | February 2015 |
Verified date | November 2021 |
Source | Brown University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate the effectiveness of Prostate Specific Membrane Antigen (PSMA ADC), as well as its safety and side effects for patients with advanced brain tumors. This study will also study how your body metabolizes (breaks down) PSMA ADC.
Status | Completed |
Enrollment | 6 |
Est. completion date | February 2015 |
Est. primary completion date | November 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Males and females Histologically confirmed GBM (Patients with gliosarcoma are also eligible) - Assessable or measurable disease by MRI - Progression after prior treatment that includes radiation, temozolomide and bevacizumab. -> 4 weeks since prior chemotherapy, bevacizumab and other systemic treatment and > 3 weeks from prior radiation. - age >18 years - Weight < 150 kg. - Karnofsky performance score > 60 - Life expectancy >12 weeks - Brain MRI within 21 days prior to registration - Laboratory results requirements - Absolute neutrophil count (ANC) = 1000/mm3. - Platelets (Plt) = 100,000/mm3 - Hemoglobin (Hgb) = 8.0 g/dL - Total bilirubin = 2.0 mg/dL - Serum alanine transferase/ Serum aspartate transaminase (ALT/AST) = 2.5x the upper limit of normal (ULN) - Serum creatinine = 2.0 mg/dL - Pancreatic Amylase (p-amylase) = the ULN - Negative serum pregnancy test for women of child-bearing potential - Stable corticosteroid dose at least 14 days prior to registration - Women of childbearing potential must have a negative pregnancy test. - Men and women of childbearing potential must be willing to consent to using effective contraception while on treatment and for at least 3 months thereafter. - Patients must not be on enzyme-inducing anti-epileptic drugs (EIAED). Patients may be on non-enzyme inducing anti-epileptic drugs (NEIAED) or may not be taking any anti-epileptic drugs. A list of AED that cause modest or no induction of hepatic metabolic enzymes will be discussed Exclusion Criteria: - Non-GBM primary invasive malignant neoplasm within the five years prior to screening except for: - keratinocyte (non-melanoma) (i.e., basal cell, squamous cell) carcinoma of the skin; or low-grade papillary superficial transitional cell carcinoma of the bladder.However, patients with stage 1 cancers not requiring cancer therapy including chemotherapy or hormone therapy, for which a lifespan of greater than 3 years without treatment is expected (such as early stage prostate cancer) may be enrolled. - Clinically significant cardiac disease (New York Heart Association Class III/ IV or severe debilitating pulmonary disease - Subjects with QTc>500 msec (either Bazzett's or Fridericia's method) - Radiation therapy, cytotoxic chemotherapy, bevacizumab or other treatment for GBM within previous three weeks - Evidence of an active infection requiring ongoing intravenous antibiotic therapy - Any toxicity = grade 2 (non-laboratory) (NCI CTCAE, Version 4.03) prior to first dose of study drug - Prior treatment with PSMA ADC or other therapies targeting PSMA, or other anti-body drug conjugate (ADC) products that contain monomethyl auristatin E (MMAE) (e.g., brentuximab vedotin, glembatumumab vedotin, ASG-5ME) - Known hypersensitivity reactions to PSMA ADC or any of its components. - Any medical condition that in the opinion of the Investigator may interfere with a subject's participation in or compliance with the study - Patients with a prior history of pancreatitis |
Country | Name | City | State |
---|---|---|---|
United States | UT Southwestern | Dallas | Texas |
United States | Rhode Island Hospital | Providence | Rhode Island |
Lead Sponsor | Collaborator |
---|---|
Heinrich Elinzano, MD | Progenics Pharmaceuticals, Inc., Rhode Island Hospital, University of Texas |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Response Rate (Progression) for Patients With Glioblastoma That Have Progressed After Prior Treatment That Has Included Radiation, Temozolomide and Bevacizumab. | The response assessment in neuro-oncology (RANO) will be used to define radiographic response.
(PD): A >25% increase in tumor area (product of two diameters) OR appearance of a new lesion/site, OR clear clinical worsening or failure to return for evaluation due to death or deteriorating condition (unless clearly unrelated to this cancer). |
3 months until progression, potentially up to 1 year | |
Secondary | Number of Patients Who Experienced Toxicities (Adverse Events) Who Received PSMA ADC for Recurrent Glioblastoma. | Please note that toxicities outlined may not all be related to the treatment regimen. | at least every 3 weeks for a maximum of 30 post coming off drug, approximately 6 months |
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