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Trial record 37 of 44 for:    Malignant Hyperthermia 5

SD-101 and BMS-986178 in Treating Patients With Advanced or Metastatic Solid Malignancies

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ClinicalTrials.gov Identifier: NCT03831295
Recruitment Status : Recruiting
First Posted : February 5, 2019
Last Update Posted : August 28, 2019
Sponsor:
Collaborator:
Bristol-Myers Squibb
Information provided by (Responsible Party):
Ronald Levy, Stanford University

Brief Summary:
This phase I trial studies the side effects of intratumoral injection of SD-101 and BMS-986178 in treating patients with solid malignancies that have spread to other places in the body. The TLR9 agonist SD-101 may stimulate the immune system in different ways and stop cancer cells from growing. BMS-986178 is a monoclonal anti-OX40 antibody that enhances the activation of T cells, immune cells that are important for fighting tumors. Giving TLR9 agonist SD-101 together with anti-OX40 antibody BMS-986178 may work better in treating patients with advanced solid tumors.

Condition or disease Intervention/treatment Phase
Advanced Malignant Solid Neoplasm Extracranial Solid Neoplasm Metastatic Malignant Solid Neoplasm Biological: Anti-OX40 Antibody BMS 986178 Drug: TLR9 Agonist SD-101 Phase 1

Detailed Description:

PRIMARY OBJECTIVES:

I. To determine the safety and tolerability of intratumoral TLR9 agonist SD-101 (SD-101) in combination with intratumoral and intravenous anti-OX40 antibody BMS 986178 (BMS-986178) in patients with advanced solid tumors.

SECONDARY OBJECTIVES:

I. To evaluate the efficacy of treatment with intratumoral SD 101 in combination with intratumoral and intravenous BMS 986178 in patients with advanced solid tumors.

II. To evaluate changes in pharmacodynamic endpoints in serial tumor biopsies from intratumor treated and untreated sites of disease.

OUTLINE:

SAFETY COHORT: Patients receive TLR9 agonist SD-101 intratumorally (IT) on days 1, 8 and 15. Patients also receive anti-OX40 antibody BMS 986178 IT on days 8 and 15, and intravenously (IV) over 30 minutes on days 8, 29 and 58.

EXPANSION COHORT: Patients receive TLR9 agonist SD-101 IT on days 1, 8 and 15. Patients also receive anti-OX40 antibody BMS 986178 IT on days 1, 8 and 15, and IV over 30 minutes on days 1, 29 and 58.

After completion of study treatment, patients are followed up every 3-6 months.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 27 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Intratumoral Injection of SD-101, an Immunostimulatory CpG Oligonucleotide, in Combination With BMS- 986178, an OX40 Agonist Antibody, in Advanced Solid Malignancies [CA012-014]
Actual Study Start Date : March 13, 2019
Estimated Primary Completion Date : June 12, 2022
Estimated Study Completion Date : June 12, 2022

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Treatment (SD-101, BMS-986178)

SAFETY COHORT: Patients receive TLR9 agonist SD-101 IT on days 1, 8 and 15. Patients also receive anti-OX40 antibody BMS 986178 IT on days 8 and 15, and IV over 30 minutes on days 8, 29 and 58.

EXPANSION COHORT: Patients receive TLR9 agonist SD-101 IT on days 1, 8 and 15. Patients also receive anti-OX40 antibody BMS 986178 IT on days 1, 8 and 15, and IV over 30 minutes on days 1, 29 and 58.

Biological: Anti-OX40 Antibody BMS 986178
Given IT or IV
Other Names:
  • BMS 986178
  • BMS-986178

Drug: TLR9 Agonist SD-101
Given IT
Other Names:
  • ISS-ODN SD-101
  • SD-101




Primary Outcome Measures :
  1. Incidence of adverse events of intratumoral injections of study drugs [ Time Frame: Up to week 96 ]

    This outcome will be measured for any participant who has received at least one dose of any study medication. Treatment-limiting toxicities will be assessed using CTCAE v5.0. All adverse events will be recorded. Treatment-limiting toxicities are defined as;

    • Hematologic toxicities: Febrile neutropenia; Grade 3 &4 thrombocytopenia; Grade 4 anemia unexplained with exception that toxicities can clearly be determined due to disease progression and/or unrelated to SD-101 or BMS-986178.
    • Non-hematological toxicity ≥ Grade 3; Alopecia; Nausea; Grade 3 or 4 electrolyte abnormalities; Grade 3 or 4 elevation of amylase or lipase not associated with pancreatitis; Grade 3 endocrinopathy controlled by hormone replacement; Grade 3 infusion reaction that returns to Grade 1 in < 6 hours; Grade 3 skin rash not requiring systemic steroid therapy or other systemic immunosuppressive therapy.
    • Doses should be delayed if any Grade ≥ 2 toxicities are not resolved to Grade ≤ 1 or baseline by next cycle.


Secondary Outcome Measures :
  1. Overall response rate [ Time Frame: Up to 3 years ]

    Tumor response assessed per Response Evaluation Criteria in Solid Tumors Criteria (RECIST v1.1) for target lesions, and assessed by physical measurement; computed tomography (CT), positron emission tomography (PET)-CT.

    • Complete Response (CR) = Disappearance of all target lesions
    • Partial Response (PR) = ≥ 30% decrease in the sum of the longest diameter of target lesions
    • Overall Response (OR) = CR + PR
    • Progressive disease (PD) = 20% increase in the sum of the longest diameter of target lesions, and/or the appearance of one or more new lesion(s)
    • Stable disease (SD) = Small changes that do not meet any of the above criteria

  2. Progression-Free survival (PFS) [ Time Frame: Up to 3 years ]
    Progression-Free Survival is defined as the time elapsed between treatment initiation (Day 1) and tumor progression or death from any cause. Progression will be defined using RECIST v1.1.



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Any advanced/metastatic, non-hematological, extracranial solid tumor malignancy with disease progression after at least one line of standard therapy or for which standard therapy known to prolong survival does not exist
  • Patients must have at least two sites of disease that are >= 10 mm in diameter, one of which must be accessible for intratumoral injection and core biopsies and the other of which must be accessible for core biopsies by interventional radiology. (Sites have to be deemed safe for repeated access upon IR review, based on anatomic location, size, shape, and accessibility). Liver lesions may not be used as the injection site even if otherwise deemed safe for access
  • Patients must have at least one additional site of measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) criteria, other than the sites selected for intratumoral injection and core biopsies
  • All patients with tumor types for which anti-PD-1 or anti PD-L1 therapy has been approved should have received such therapy prior to enrollment, with evidence of progression on at least two scans (ie, with pseudoprogression ruled out). Patients with validated driver mutations should have received and progressed on appropriate targeted therapy
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Life expectancy of at least three months
  • Total bilirubin < 1.5 x upper limit of normal (ULN) (unless patient has history of Gilbert?s disease)
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) < 3 x upper limit of normal (ULN)
  • Creatinine < 1.5 x ULN or measured or calculated creatinine clearance (glomerular filtration rate [GFR] can also be used in place of creatinine or creatinine [CrCl]) >= 60 mL/min for subject with creatinine levels > 1.5 x ULN
  • Absolute neutrophil count (ANC) >= 1,500/mcL
  • Hemoglobin >= 9 g/dL without transfusion within the past 4 weeks
  • Platelets >= 100,000/mcL
  • Prothrombin time (PT)/international normalized ratio (lNR) within normal limits
  • Written informed consent obtained from subject
  • Patients who have previously received an immune checkpoint inhibitor prior to enrollment must have any immune related toxicities resolved to =< grade 1 or baseline (prior to the checkpoint inhibitor) to be eligible. Patients who developed endocrine adverse events on checkpoint inhibitor are eligible to enter regardless of the Common Terminology Criteria for Adverse Events (CTCAE) Grade resolution as long as the patient is well controlled on endocrine replacement
  • Women of childbearing potential must have a urine or serum pregnancy test within 24 hours prior to the first dose of trial treatment. If the urine test is positive or cannot be confirmed as negative, then a serum test will need to be negative
  • Women of childbearing potential must practice a highly effective method of birth control during treatment and for 160 days after treatment completion. Women of childbearing potential who chose complete abstinence must agree to have a urine or serum pregnancy tests within 24h of each dose of study treatment. If the urine test is positive or cannot be confirmed as negative, then a serum test will need to be negative
  • Men who are sexually active with women of childbearing potential must agree to follow instructions for methods of contraception while being treated on the study, and for 165 days after treatment completion. Men must agree to not donate sperm during this time period

Exclusion Criteria:

  • History of grade 2 or higher hypersensitivity reaction to either SD-101 or BMS-986178
  • Patients who require immediate treatment or cytoreduction, as deemed by their physician or the study investigators
  • Treatment with other anticancer therapy (chemotherapy, small molecule, or radiation therapy) within the past 3 weeks prior to study entry or within the past 6 weeks prior to study entry for immunotherapies
  • Use of investigational agent within the past 3 weeks prior to study enrollment
  • Major surgery within 4 weeks of enrollment, or a wound that has not fully healed
  • Vaccinated with live, attenuated vaccines within 4 weeks of enrollment
  • Symptomatic central nervous system (CNS) metastases
  • Known bleeding disorder that is deemed to place the patient at unacceptable risk for bleeding complications from intratumoral injection. Patients on anticoagulants and anti-platelet agents other than aspirin are excluded
  • Any uncontrolled bacterial, fungal, viral, or other infection
  • Active autoimmune disease requiring systemic treatment within the past 2 years, with the exception of patients well controlled on physiologic endocrine replacement
  • Treatment with corticosteroids (> 10 mg per day prednisone or equivalent) or other immune suppressive drugs within 14 days prior to initiation of study drug. Steroids for topical ophthalmic, inhaled, or nasal administration are allowed. Patients requiring courses of systemic steroids for 14 consecutive days or less for an acute condition (not for a chronic autoimmune illness) may receive study drug 14 days after steroid therapy
  • Patients with a history of other prior malignancy with the exception of non-melanoma skin cancer, carcinoma in situ of the cervix, in situ carcinoma of the bladder, or other malignancy that has undergone potentially curative therapy with no evidence of disease for the last > 2 years and is deemed by the investigator to be a low risk for recurrence
  • Significant cardiac disease (New York Heart Association [NYHA] class IV congestive heart failure, or unstable angina or myocardial infarction within the past 6 months)
  • Human immunodeficiency virus (HIV) positive (+) patients or patients with active hepatitis B or C infection
  • Patients who are pregnant or breastfeeding
  • Any other medical history, including laboratory results, deemed by the investigator likely to interfere with their participation in the study, or to interfere with the interpretation of the results

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03831295


Contacts
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Contact: Melanie Ashland 650-736-0224 mashland@stanford.edu

Locations
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United States, California
Stanford Cancer Institute Palo Alto Recruiting
Palo Alto, California, United States, 94304
Contact: Melanie Ashland    650-736-0224    mashland@stanford.edu   
Principal Investigator: Shivaani Kummar         
Sponsors and Collaborators
Ronald Levy
Bristol-Myers Squibb
Investigators
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Principal Investigator: Shivaani Kummar Stanford Cancer Institute Palo Alto

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Responsible Party: Ronald Levy, Robert K. and Helen K. Summy Professor in the School of Medicine, Stanford University
ClinicalTrials.gov Identifier: NCT03831295     History of Changes
Other Study ID Numbers: IRB-48546
NCI-2019-00251 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
VAR0175 ( Other Identifier: OnCore )
IRB-48546 ( Other Identifier: Stanford IRB )
First Posted: February 5, 2019    Key Record Dates
Last Update Posted: August 28, 2019
Last Verified: August 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Additional relevant MeSH terms:
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Neoplasms
Antibodies
Immunoglobulins
Immunologic Factors
Physiological Effects of Drugs