G-202 in the Neoadjuvant Setting Followed by Radical Prostatectomy in Patients With Prostate Cancer

NCT ID: NCT02381236

Last Updated: 2017-02-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-02-29
• Study Completion Date: 2017-02-28

Brief Summary

A single-arm, open-label Phase II clinical trial to evaluate the effect of G-202 on the perfusion and volume of the prostate using non-invasive multiparametric prostate magnetic resonance imaging (mpMRI).

Detailed Description

More than one-third of patients with localized high-risk prostate cancer who undergo radical prostatectomy eventually relapse with distant disease and some data suggest that neoadjuvant treatment in this patient population may be helpful. This study is based on prodrug tumor targeting, in which an inactive form of a toxic agent is administered systemically and gets activated in specific locations in the body, resulting in higher concentrations of the cytotoxic form at the tumor location. G-202 is a prodrug that is activated in prostate cancer tissue and in the blood vessels of tumors, but not normal tissue; once activated, G-202 leads to disruption of intracellular calcium levels and subsequent induction of apoptosis. Thus, G-202 is expected to bring about cell death in prostate cancer cells and to destroy the blood supply of prostate tumors. G-202 has led to disease stabilization in some patients, but the drug has not been evaluated in the neoadjuvant setting. This single-arm, open-label Phase II clinical trial will evaluate the safety and activity of G-202 in patients with localized high-risk prostate cancer prior to radical prostatectomy. Through its effects on the neovasculature of tumors, G-202 is anticipated to disrupt the blood supply of the prostate tumor, resulting in decreased perfusion and subsequent tumor volume. The primary endpoint of this study is evaluation of G-202 on the perfusion and volume of the prostate using non-invasive multiparametric prostate magnetic resonance imaging (mpMRI).

Conditions

Prostatic Neoplasms

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

G-202

G-202 administered by intravenous infusion on 3 consecutive days of a 28-day cycle

Group Type: EXPERIMENTAL

G-202

Intervention Type: DRUG

G-202 administered by intravenous infusion on Days 1, 2 and 3 of each 28-day cycle for up to 3 cycles

Interventions

G-202

G-202 administered by intravenous infusion on Days 1, 2 and 3 of each 28-day cycle for up to 3 cycles

Intervention Type: DRUG

Other Intervention Names

Mipsagargin

Eligibility Criteria

Inclusion Criteria

• ECOG Performance Status < 2
• Histological confirmation of prostatic adenocarcinoma that is confined to the prostate without evidence of regional and/or distant metastasis
• Clinical stage T1c or T2a with high-grade disease (Gleason 8-10) on initial biopsy, clinical stage T2b-T2c with Gleason grade 7 (4+3), or clinical stage T3
• Negative bone scan and CT of chest and abdomen within 6 weeks of first infusion of G-202
• Candidate for radical prostatectomy
• Adequate hematologic function (ANC ≥ 1200/mm3, hemoglobin ≥ 8.5 g/dL, platelets ≥ 75,000/mm3)
• Adequate hepatic function (albumin ≥ 2.8 g/dL, AST and ALT ≤ 5 x ULN, total bilirubin < 2 mg/dL)
• Adequate renal function (proteinuria level ≤ 2+, serum creatinine ≤ 1.5 x ULN)
• Acceptable coagulation profile (no history of substantial non-iatrogenic bleeding diatheses, INR ≤ 2.3, aPTT ≤ 1.5 x ULN)
• Ejection fraction (LVEF) ≥ 45% measured by echocardiogram
• Willing to use acceptable methods of contraception to avoid pregnancy

Exclusion Criteria

• Prostatic adenocarcinoma with neuroendocrine differentiation or small cell features
• Unable to tolerate mpMRI
• Surgical resection or major surgery within 4 weeks or stereotactic biopsy within 1 week prior to first G-202 treatment
• Previous or current hormonal treatment, chemotherapy, radiation therapy, immunotherapy, or other investigational status drug for prostatic adenocarcinoma
• Currently requiring systemic administration of antibiotics or chronic administration of anti-viral agents
• Use of anti-coagulants is limited to local use for control of central line patency
• History or evidence of cardiac risk
• Uncontrolled cardiac or coronary artery disease
• Uncontrolled hypertension or hypertension requiring treatment with more than 2 anti-hypertensive agents
• Severe or uncontrolled medical disease
• Severe gastrointestinal bleeding within 12 weeks prior to treatment with G-202
• Known history of HIV, hepatitis B or hepatitis C
• Use of herbal products that may decrease PSA levels (e.g., saw palmetto) or systemic corticosteroids
• Documentation of keratosis follicularis
• Requirement for chronic use of medications known to be strong inhibitors or inducers of cytochrome (CYP3A4) iso-enzymes
• Another primary malignancy, except non-melanoma skin cancer, that has not been in remission for at least 2 years.

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

GenSpera, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Robert Amato, D.O.

Role: PRINCIPAL_INVESTIGATOR

University of Texas Health Sciences Center at Houston

Locations

University of Texas Health Sciences Center

Houston, Texas, United States

Countries

United States

Other Identifiers

G-202-005

Identifier Type: -

Identifier Source: org_study_id