Phase 1b Maintenance Therapy Study of ONT-10 in Patients With Solid Tumors

Sponsor

Cascadian Therapeutics Inc. (Industry)

Overall Status

Completed

CT.gov ID

NCT01978964

Collaborator

(none)

Enrollment

Location

Arm

Duration (Months)

2.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is an open label phase 1b maintenance therapy study to evaluate the long-term safety, immunogenicity, and anti-tumor effects of repeat-dose vaccination with ONT-10 in patients who have demonstrated safety and clinical benefit on the original ONT-10-001 phase 1 study.

Condition or Disease	Intervention/Treatment	Phase
Solid Tumors	Biological: ONT-10	Phase 1

Detailed Description

Open label Phase 1b maintenance therapy study to evaluate the long-term safety, immunogenicity, and anti-tumor effects of repeat-dose vaccination with ONT-10 in patients with previously treated Stage 3 or 4 solid tumors with histologies that have been associated with expression of the MUC1 antigen as described in the medical literature. Patients must have previously been enrolled on the Phase 1 clinical trial ONT-10-001, completed all treatment and follow-up through at least 12 weeks, experienced no dose limiting toxicity, and experienced no progression of disease per the immune-related Response Criteria. Patients will receive maintenance ONT-10 every 6 weeks.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

90 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Maintenance Therapy With ONT-10, a Liposomal MUC1 Cancer Vaccine, in Patients Who Have Previously Received ONT-10

Study Start Date :

Nov 1, 2012

Actual Primary Completion Date :

Mar 1, 2016

Actual Study Completion Date :

Mar 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: ONT-10 Vaccine	Biological: ONT-10 ONT-10 is a liposomal synthetic glycopolypeptide antigen formulated with PET Lipid A adjuvant

Arm

Intervention/Treatment

Experimental: ONT-10 Vaccine

Biological: ONT-10

ONT-10 is a liposomal synthetic glycopolypeptide antigen formulated with PET Lipid A adjuvant

Outcome Measures

Primary Outcome Measures

Incidence and severity of adverse events and lab abnormalities [20-60 weeks]

Secondary Outcome Measures

Immunogenicity and anti-tumor activity [20-60 weeks]
Assessments of humoral and cellular immune response and overall response as per irRC and RECIST 1.1.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 70 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Was enrolled on the Phase 1 clinical trial ONT-10-001 and:

completed all treatment and follow-up through at least 12 weeks
experienced no dose limiting toxicity (DLT)
experienced no progression of disease per the irRC1
Patients enrolling in the retreatment cohort may have experienced localized disease progression that was treated with definitive therapy to return the patient to a state of stable disease. Examples include localized disease progression treated with complete surgical resection, a solitary brain metastasis treated with complete surgical resection or curative intent stereotactic radiosurgery, or a solitary bone metastasis that is treated with curative-dose radiation therapy.
Patients enrolling on the retreatment cohort must have locally and systemically stable disease following the definite local treatment.

Last received ONT-10 a maximum of 6 months (unless approved by the medical monitor) prior to receiving the first dose of maintenance or retreatment cohort therapy
ECOG 0 or 1
Adequate baseline hematological parameters as defined by white blood cell count (WBC) ≥ 3.5 x 103/µL, lymphocyte count ≥ 1.0 x 103/µL, platelet count ≥ 100 x 103/µL, and hemoglobin ≥ 9 g/dL
Adequate hepatic parameters as defined by total bilirubin ≤ 1.5 x upper limit of normal (ULN) and aspartate aminotransferase (AST/SGOT) and alanine aminotransferase (ALT/SGPT) ≤ 3 x ULN
Serum creatinine ≤ 1.5 x ULN
Resolution of all prior ONT-10 related toxicities to ≤ Grade 1in severity
If female of child bearing potential, have a negative pregnancy test at screening
If fertile male or female of child-bearing potential, agree to consistently use a highly effective method of birth control (including birth control pills, barrier device, or intrauterine device) from the time of consent through 3 months following the last dose of study drug
Be able and willing to sign informed consent document that has been approved by an institutional review board or independent ethics committee (IRB/IEC)

Exclusion Criteria:

Has medical, social, or psychosocial factors that, in the opinion of the investigator, could impact safety or compliance with study procedures
Received treatment with any systemic chemotherapy, experimental agent, or radiation therapy (with the exception of palliative localized radiation therapy) following completion of treatment on the ONT-10-001 study
Known history of autoimmune disease, arteritis, or vasculitis, including, but not limited to: lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease (including ulcerative colitis and Crohn's disease), Grave's disease, Hashimoto's thyroiditis, Wegener's granulomatosis, temporal arteritis, and polyarteritis nodosa
Has untreated or uncontrolled central nervous system (CNS) metastases, including patients who require glucocorticoid therapy for CNS metastases
Known immunodeficiency disease, including cellular immunodeficiencies, hypogammaglobulinemia, or dysgammaglobulinemia; and/or other hereditary or congenital immunodeficiencies
Chronic steroid or immunosuppressive therapy (except for low dose corticosteroids for chronic obstructive pulmonary disease [COPD] or topical steroids, which are allowed)
Known to be positive for human immunodeficiency virus (HIV), hepatitis B, or hepatitis C
Administration of any vaccine ≤ 4 weeks prior to first maintenance or retreatment cohort dose of ONT-10 with the exception of influenza, pneumococcus, and Tdap