- Solid Tumors
- Pipeline Molecules
- Alliance Partners
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Currently, you can access the following clinical trials being conducted worldwide:
Clinicaltrials.gov identifier NCT02767557
Recruitment Status Recruiting
First Posted May 10, 2016
Last update posted April 21, 2020
This is a multicenter center, 2-arms prospective randomized phase II trial which evaluates whether tocilizumab with gemcitabine/nab-paclitaxel is more effective than gemcitabine/nab-paclitaxel.
The development of new effective treatment strategies remains a major challenge in patients with PC. High levels of IL-6 and presence of a systemic inflammatory response in PC patients have been reported to correlate with worse survival. Preclinical PC models have clearly shown that anti-IL-6-receptor antibody tocilizumab in combination with chemotherapy reduced tumor growth, number of distant metastases and the local recurrence rate. Thus, blockade of IL-6-regulated signaling pathways represents a promising approach in combination with chemotherapy. Elevated C-reactive protein (CRP) alone or in combination with hypoalbuminaemia (Modified Glasgow Prognostic Score - mGPS) are induced by IL-6 and could feasibly represent surrogate markers for IL-6 bioactivity to stratify patients likely to gain benefit through targeting IL-6.
|Experimental: Tocilizumab & Gemcitabine and nab-Paclitaxel
Tocilizumab: 8 mg/kg given I. V. on day 1 over 60 minutes every 28 day cycle. Gemcitabine: 1000 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle. Nab-Paclitaxel: 125 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle.
|Active Comparator: Gemcitabine and nab-Paclitaxel
Gemcitabine: 1000 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle. Nab-Paclitaxel: 125 mg/m² I. V. on day 1, day 8 and day 15 of every 28 day cycle.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, , Learn About Clinical Studies.-->
- Signed informed consent
- Histological or cytological pancreatic adenocarcinoma. Malignant unspecified tumor
cells in cytological specimen are allowed after investigator assessment, mixed
histology including adenosquamous carcinoma is allowed
- Male or non-pregnant, non-lactating females who are ≥18 years of age at the time of
signing the informed consent form (ICF)
- Non-curable unresectable locally advanced or metastatic pancreatic carcinoma.
- A modified Glasgow Prognostic Score (mGPS) criteria of 1 or 2 assessed within 14 days
of randomization as defined below:
- mGPS of 1: CRP > 10 mg/L and albumin ≥ 35 g/L
- mGPS of 2: CRP > 10 mg/L and albumin < 35 g/L - No prior antineoplastic chemotherapy or anti-cancer drugs. Patients who have received neoadjuvant or adjuvant chemotherapy and who are diagnosed with loco regional recurrent or metastatic disease are not eligible - ECOG/WHO Performance Status (PS) 0-1 - ≥ 4 weeks since prior major surgery, ≥ 2 weeks since prior minor surgery and ≥ 1 week since prior radiation therapy - Measurable disease using the RECIST1.1 criteria, defined as lesions that can be measured in at least one dimension and which have not been previously irradiated. Longest diameter ≥ 20 mm with conventional techniques or ≥ 10 mm with spiral CT scan or MRI - Fertile men and women of childbearing potential (defined as a sexually mature woman who (1) has not undergone hysterectomy [the surgical removal of the uterus] or bilateral oophorectomy [the surgical removal of both ovaries] or (2) has not been naturally postmenopausal for at least 24 consecutive months [ie, has had menses at any time during the preceding 24 consecutive months]) must use secure contraception methods as follows: intrauterine device, double-barrier contraception, as a condom and occlusive cap (diaphragm or cervical/vault caps) with a vaginal spermicidal agent (foam/gel/cream/suppository), vasectomized partner who is sterile prior to the female subject's entry and is the sole sexual partner for that female, or complete abstinence from sexual intercourse from before 2 months entering the study until 6 months after end of chemotherapy - Acceptable hematology parameters defined as: - Absolute neutrophil count (ANC) ≥ 1.5 x 10⁹/L - Platelet count ≥ 100 x 10⁹/L - Haemoglobin ≥ 5.6 mmol/L - Acceptable liver function defined as: - Serum bilirubin < 1.5 x upper limit of normal (ULN) - ASAT/ALAT < 2.5 x ULN ( < 5 x ULN with known liver metastasis) - Acceptable renal function with a creatinine clearance ≥ 50 mL/min/ (eg, using the Cockroft-Gault formula) - Subjects must have signed and dated a BIOPAC IRB/IEC approved written informed consent form in accordance with regulatory and institutional guidelines. This must be obtained before the performance of any protocol related procedures that are not part of normal subject care Exclusion Criteria: - Electrocardiogram (ECG) with significant modifications suggesting a high risk of occurrence of angina pectoris or high risk of arrhythmia. - Other malignancies, except adequately treated basal carcinoma or squamous cell carcinoma of the skin or in-situ cervix carcinoma or incidental prostate cancer (T1a, Gleason score ≤ 6, PSA < 0.5 ng/ml), or any other tumor with a disease free survival of ≥ 5 years. - History of serious or concurrent illness or uncontrolled medical disorder; any medical condition that might be aggravated by chemotherapy treatment or which could not be controlled; including, but not restricted to: - Active infection requiring antibiotics within 2 weeks before the study inclusion - Concurrent congestive heart failure NYHA ( class III - IV ) - Unstable angina pectoris, or myocardial infarction within 6 months and/or prior poorly controlled hypertension - Inflammatory bowel disease (colitis, Crohns) or other serious gastrointestinal conditions associated with risk of perforation - Peripheral neuropathy grade ≥ 2 according to CTCAE v 4.0 - Concomitant use of immunosuppressive or myelosuppressive medications that would in the opinion of the investigator, increase the risk of serious neutropenic complications. - No known or suspected allergy to the investigational agents or any agents given in association with this trial. - Pregnant or lactating women. - Any psychological, familial, sociological, or geographical condition which does not permit protocol compliance and medical follow-up. - Enrollment in any other clinical protocol or investigational study with an interventional agent or assessments that may interfere with study procedures.
Contact: Inna Chen, MD +45 38682898 Inna.Chen@regionh.dk
Contact: Dorte Nielsen, MD DMSc +45 38682344 Dorte.Nielsen.email@example.com
Herlev & Gentofte University Hospital, Denmark
Department of Oncology
Principal Investigator: Inna Chen, MD Herlev & Gentofte Hospital
Principal Investigator: Olav Dajani, MD PhD Oslo University Hospital