A Pilot, Prospective, Non-randomized Evaluation of the Safety of Anakinra Plus Standard Chemotherapy
NCT ID: NCT02021422
Last Updated: 2017-01-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE1
13 participants
INTERVENTIONAL
2013-06-30
2017-12-31
Brief Summary
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Detailed Description
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This is a pilot, prospective, non-randomized, consecutive enrollment study that will enroll up to 12 subjects who meet the study defined inclusion and exclusion criteria.
Subjects will undergo standard of care chemotherapy treatment/regimens (i.e., modified FOLFIRINOX). Subjects will be dispensed a 2 weeks supply of anakinra the day they begin chemotherapy. They will be instructed to begin self-administering the anakinra (study drug) injections the day after their first dose of chemotherapy.
They will have a blood sample collected at baseline and 6 months follow up. If they have surgery for their disease, they may have a tissue sample collected for later analysis.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Anakinra with Modified Folfirinox
8-weeks of anakinra and modified FOLFIRINOX regimen (refer to Appendix 9 for regimen) as follows
Kineret (anakinra) Dosage Route Administration 100 mg SC Every Other Day
Modified FOLFIRINOX Drug Dose Administration Oxaliplatin 85 mg/m2 2-4 hours Irinotecan 180 mg/m2 90 minutes fluorouracil 2400 mg/m2 48 hours
anakinra
Dosage Route Administration 100 mg SC Every Other Day
Oxaliplatin
Oxaliplatin 85 mg/m2 2-4 hours
Irinotecan
Irinotecan 180 mg/m2 90 minutes
fluorouracil
fluorouracil 2400 mg/m2 48 hours
Interventions
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anakinra
Dosage Route Administration 100 mg SC Every Other Day
Oxaliplatin
Oxaliplatin 85 mg/m2 2-4 hours
Irinotecan
Irinotecan 180 mg/m2 90 minutes
fluorouracil
fluorouracil 2400 mg/m2 48 hours
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Male or non-pregnant and non-lactating female
* Confirmed metastatic/inoperable metastatic pancreas cancer and/or Histologically/cytologically confirmed metastatic adenocarcinoma of pancreas
* Patients' blood counts and blood chemistry levels at baseline must be not clinically significant (NCS) as determined by the enrolling investigator.
* Patient has Eastern Cooperative Oncology Group( ECOG ) Performance Status 0 to 2 (refer to Appendix 5):
* Signed study consent form
Exclusion Criteria
* Pregnant or lactating female
* Patient has islet cell neoplasms
* Active secondary malignancies (2nd cancer not treated/present)
* Active, uncontrolled bacterial, viral, or fungal infection(s) requiring systemic therapy
* Known infection with hepatitis B, hepatitis C, or cirrhosis
* Major surgery or vascular device placement (excluding ports for IV medication/chemotherapy) within 2 weeks prior to Day 1 of treatment in study
* History of allergy or hypersensitivity to the study drugs
* Patient is enrolled in any concurrent-outside (outside Baylor University Medical Center or Texas Oncology) clinical protocol or investigational trial
* Significant cardiac disease as defined as New York Heart Association (NYHA) classification III or IV, uncontrolled CHF, or prior MI last 6-months
* Any prior gastrointestinal (GI) disease or history of prior pelvic or abdominal radiation which in the opinion of the investigator may place the patient at increased risk
* Peripheral sensory neuropathy ≥ to grade 2 at baseline
* Significant co-morbidities deemed by investigator as unsuitable for participation/enrollment
* Study consent form not signed
18 Years
ALL
No
Sponsors
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Baylor Research Institute
OTHER
Responsible Party
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Principal Investigators
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Carlos Becerra, MD
Role: PRINCIPAL_INVESTIGATOR
Baylor Sammons Cancer Center
Locations
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Baylor Sammons Cancer Center
Dallas, Texas, United States
Countries
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References
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Other Identifiers
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013-018
Identifier Type: -
Identifier Source: org_study_id
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