Kidney Cancer Clinical Trial
A Rollover Protocol for Subjects Previously Treated With AGS-003
Summary
The purpose of this study is to evaluate clinical response to AGS-003 alone or in combination with sunitinib therapy.
Full Description
AGS-003-005 is a rollover, open label, Phase II clinical study testing the biologic activity and safety of AGS-003 in subjects who have experienced either partial responses or prolonged stable disease and continue to benefit from ongoing treatment with AGS-003 in protocols AGS-003-004 or AGS-003-006.
Rollover subjects from AGS-003-004 will continue with AGS-003 monotherapy booster dosing until disease progression or until a discontinuation criterion is reached.
Subjects that progress on AGS-003 monotherapy (from the AGS-003-004 protocol) may start sunitinib treatment and re-initiate AGS-003 therapy beginning with the induction phase dosing schedule.
Rollover subjects from AGS-003-006 will continue sunitinib dosing in combination with booster dosing of AGS-003 until disease progression or until a discontinuation criterion is reached.
If a subject has disease progression due to a new tumor lesion, upon consultation between the investigator, Argos representatives and the Argos medical monitor, the subject may be considered for re-manufacture of study product (from the new metastatic lesion) and dosing with this new product in combination with sunitinib beginning with the induction phase dosing schedule.
For those subjects initiating treatment with the induction phase as described above, restaging imaging occurs at screening (baseline), prior to the fifth dose in the induction phase (as applicable) and every 12 weeks during the booster phase (at the start of the sunitinib holiday, 2 weeks prior to the next AGS-003 dose).
For subjects on combination therapy, if dosing with sunitinib is stopped due to sunitinib-related issues, treatment with AGS-003 may continue.
Close-out visits will occur upon disease progression (other than circumstances discussed above which are eligible for re-induction) or upon decision to terminate the study by the sponsor.
Quarterly follow-up for survival for each subject will occur by telephone interview for 1 year following the last AGS-003 administration or study termination.
Eligibility Criteria
Inclusion Criteria:
Age ≥ 18 years
Subjects are receiving ongoing treatment with AGS-003 in protocol AGS- 003-004 or AGS-003-006.
Measurable disease that can be monitored per RECIST throughout the course of study participation.
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Adequate hematologic function, as defined by the following criteria:
White blood cell (WBC) ≥ 4000/µL (≥ 4.0 x 103/µL)
Absolute neutrophil count (ANC) ≥ 1500/µL (≥ 1.5 x 103/µL)
Platelets ≥ 100,000/µL (≥ 100 x 103/µL)
Hemoglobin (Hgb) ≥ 9.0 g/dL
Adequate renal and hepatic function, as defined by the following criteria:
Serum creatinine ≤ 1.5 x upper limit of normal (ULN) or, if serum creatinine > 1.5 x ULN, estimated glomerular filtration rate (eGFR) ≥ 30 mL/min
Total serum bilirubin ≤ 1.5 x ULN
Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN, or AST and ALT ≤ 5 x ULN if liver function abnormalities are due to underlying malignancy
Adequate coagulation function as defined by the following criteria:
Prothrombin time (PT) ≤ 1.5 x ULN
Activated partial thromboplastin time (PTT) < 1.5 x ULN
Corrected calcium ≤ 11.5 mg/dL
Negative serum pregnancy test for female subjects with reproductive potential, and agreement of all male and female subjects of reproductive potential to use a reliable form of contraception during the study and for 12 weeks after the last dose of study drug
Able to abstain from taking prohibited drugs, either prescription or non- prescription, during the treatment phase of the study
Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures
Signed and dated informed consent document indicating that the subject (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment
No brain metastases detected by magnetic resonance imaging (MRI).
Exclusion Criteria:
Any serious medical condition considered by the investigator to constitute an unwarranted high risk for investigational treatment
History of or known brain metastases, spinal cord compression, or carcinomatous meningitis, or evidence of brain or leptomeningeal disease on screening computed tomography (CT) scan or MRI
Pregnancy or breastfeeding
Active autoimmune disease or condition requiring chronic immunosuppressive therapy
NOTE: Abnormal laboratory values for autoimmunity markers in the absence of other signs/symptoms of autoimmune disease are not exclusionary.
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There is 1 Location for this study
Minneapolis Minnesota, 55455, United States
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