Study of G-202 (Mipsagargin) as Second-Line Therapy Following Sorafenib in Hepatocellular Carcinoma

Advanced Adult Hepatocellular Carcinoma Clinical Trial

— G-202-003  

Official title:

A Phase II, Multicenter, Single-Arm Study of G-202 (Mipsagargin) as Second-Line Therapy Following Sorafenib for Adult Patients With Progressive Advanced Hepatocellular Carcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01777594
• Other study ID #: G-202-003
• Status: Completed
• Phase: Phase 2
• First received: January 18, 2013
• Last updated: August 18, 2016
• Start date: January 2013
• Est. completion date: March 2015

Study information

• Verified date: August 2016
• Source: GenSpera, Inc.
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug AdministrationUnited States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

Hepatocellular carcinoma (HCC) is the fifth most common type of cancer worldwide and the third most common cause of death from cancer. Sorafenib is the only approved therapy for treatment of advanced HCC, and there is a need to identify more drugs that are beneficial for these patients without unacceptable side effects. Prodrug chemotherapy is an approach in which an inactive non-toxic agent is administered to the patient and gets activated within the body at specific locations, resulting in a higher concentration of the cytotoxic form at a tumor location while avoiding general side effects. G-202 (mipsagargin) is an example of prodrug chemotherapy. It is activated by Prostate Specific Memory Antigen (PSMA), which is expressed by some cancer cells and in the blood vessels of most solid tumors, but not by normal cells or blood vessels in normal tissue. It is believed that activation of the prodrug G-202 will allow the drug to kill cancer cells. This study will evaluate the activity and safety of G-202 in patients with hepatocellular carcinoma who have progressed after taking sorafenib. The study will evaluate clinical activity and safety of G-202 administered by intravenous infusion on three consecutive days of a 28-day cycle.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: March 2015
• Est. primary completion date: March 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Informed consent document signed prior to the performance of any study-specific procedures and initiation of study therapy

• At least 18 years of age

• ECOG Performance Status 0 or 1

• Histologic or cytologic confirmation of hepatocellular carcinoma (HCC)

• Child-Pugh score of A or B7

• At least one measurable lesion (preferably in the liver) assessed within 4 weeks of first administration of G-202 by abdominal CT or MRI with dynamic phase imaging of the liver, pelvic CT or MRI with contrast, chest CT with contrast, and bone imaging in patients with known bone metastases or if medically indicated

• Must have received sorafenib therapy and had disease progression on sorafenib therapy or was not able to tolerate sorafenib

• Sorafenib or other anti-cancer therapy must have been discontinued > 21days prior to the first administration of G-202

• Adequate hematologic function (ANC = 1200/mm3, hemoglobin = 8.5 g/dL, platelet count = 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 (PT/INR = 2.3, aPTT = 1.5 x ULN)

• Acute toxicity from previous therapy (excluding alopecia) must have resolved to = Grade 1 per CTCAE v4.0

• Negative serum pregnancy test for women of child-bearing potential

Exclusion Criteria:

• Prior locoregional therapies (e.g., transarterial chemoembolization [TACE]) = 4 weeks prior to the first administration of G-202 or not recovered from treatment-related toxicities.

• Radiotherapy = 4 weeks prior to the first administration of G-202 or not recovered from toxicities (palliative radiotherapy for bone lesions = 2 weeks prior allowed)

• Major surgery = 4 weeks prior to first administration of G-202

• Intolerance to both CT and MRI contrast agents

• Candidate for liver transplantation

• Persistent or untreated biliary infection

• Any GI bleeding within 12 weeks prior to first administration of G-202

• Currently receiving any full-dose anti-coagulation treatment

• Clinically-significant third space fluid accumulation

• Known CNS metastasis, including brain metastasis or leptomeningeal metastasis

• Known human immunodeficiency virus (HIV) positivity

• Viral hepatitis requiring anti-viral therapy

• History or evidence of cardiac risk, including screening QTc interval > 470 msec, clinically-significant uncontrolled arrhythmias or arrhythmia requiring treatment (except atrial fibrillation and paroxysmal supraventricular tachycardia), history of acute coronary syndromes within 6 months (including myocardial infarction and unstable angina, coronary artery bypass graft, angioplasty, or stenting) or history of congestive heart failure with most recent ejection fraction < 45%

• Uncontrolled hypertension (systolic BP = 160 or diastolic BP = 100)

• Cerebrovascular accident or transient ischemic attack within 6 months prior to the first dose of study therapy

• History of pulmonary embolism within 6 months or untreated deep venous thrombosis

• Documentation of keratosis follicularis (also known as Darier or Darier-White disease)

• Requirement for chronic use of inhibitors or inducers of cytochrome (CYP3A4) iso-enzymes

• Known hypersensitivity to any study drug component, including thapsigargin derivatives, polysorbate 20, or propylene glycol

• Known history of another primary malignancy that has not been in remission for at least 2 years (non-melanoma skin cancer, cervical carcinoma in situ or squamous intraepithelial lesions allowed)

• Use of any investigational agent within 4 weeks prior to the first administration of G-202

• Pregnancy or nursing

• Any medical intervention, other medical condition, psychiatric condition or social circumstance which could compromise patient safety and/or adherence with study requirements

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Advanced Adult Hepatocellular Carcinoma
• Carcinoma
• Carcinoma, Hepatocellular

Intervention

Drug:
• G-202
G-202 administered by intravenous infusion (IV, in the vein) on Days 1, 2 and 3 of each 28-day cycle until progression or development of unacceptable toxicity

Locations

Country	Name	City	State
United States	Mary Crowley Cancer Research Center	Dallas	Texas
United States	Oncology Consultants, PA	Houston	Texas
United States	University of Texas Health Sciences Center at Houston, Memorial Hermann Cancer Center	Houston	Texas
United States	The University of Texas Health Science Center at San Antonio	San Antonio	Texas

Sponsors (1)

Lead Sponsor	Collaborator
GenSpera, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to progression	Duration of time from the first administration of G-202 to the time of radiologic progression	every 8 weeks, until disease progression (estimated up to 2 years)	No
Secondary	Overall response rate	Percentage of patients with complete response (CR), partial response (PR) or stable disease (SD) after treatment with G-202	every 8 weeks, until disease progression (estimated up to 2 years)	No
Secondary	Progression-free survival	Duration of time from the first administration of G-202 to the time of radiologic progression or death	every 8-12 weeks, until disease progression or death (estimated up to 3 years)	No
Secondary	Overall survival	Duration of time from the first administration of G-202 to the time of death	every 12 weeks for approximately 3 years or until patient death	No