Gemcitabine and ON 01910.Na in Previously Untreated Metastatic Pancreatic Cancer

Completed · Phase 3

Conditions studied: Metastatic Pancreatic Adenocarcinoma

In brief

The question being asked in this study is: Will patients with advanced pancreatic cancer live significantly longer if they are treated with a combination of Gemcitabine and ON 01910.Na than if they are treated with Gemcitabine alone? There are two parts to this study. In the first part of the study, patients with metastatic pancreatic cancer who have received no prior chemotherapy for this disease will be assigned by chance either to the group that will be treated with both Gemcitabine and ON 01910.Na (about 100 patients will be in this group) or, to the group that will be treated with Gemcitabine only (about 50 patients will be in this group). How long patients survive in the 2 groups will be compared. If it looks like there is no difference between the groups, the study will stop. If it looks like patients in the group that were treated with both Gemcitabine and ON 01910.Na survive longer, the study will continue into a second part where more patients will be treated in order to confirm and better understand the findings of the first part of the study.

Key facts

Study ID: NCT01360853
Run by: Traws Pharma, Inc.
People needed: 160
Starts: 2011-05-01
Expected to finish: 2015-12-01
Last updated by the study team: 2016-08-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Patients at least 18 years old presenting with histopathologically or cytologically confirmed metastatic adenocarcinoma of the pancreas; metastatic disease is defined as disease which has spread beyond the peri-pancreatic lymph nodes.
Patients must have received no prior chemotherapy for pancreatic cancer, including adjuvant chemotherapy.
Measurable disease, defined as lesions that can be accurately measured in at least 1 dimension with longest diameter (LD) ≥20 mm using conventional techniques or ≥10 mm with spiral computed tomography (CT) scan; measurable lymph nodes must be ≥15 mm in the short axis.
ECOG Performance Status of 0, 1, or 2.
Patients must have adequate renal function and serum creatinine ≤2.0 mg/dL.
Patients must have adequate liver function as defined by total bilirubin ≤2.0 mg/dL and transaminase levels no higher than 3.0 times the institution's upper limit of normal (ULN). Patients with hepatic metastases may have transaminase levels of up to 5.0 times the ULN.
All patients must have a serum albumin ≥3.0 g/dL.
Patients must have adequate bone marrow (BM) function as defined by a granulocyte count ≥1,500/mm3, a platelet count ≥100,000/mm3, and hemoglobin >9 g/dL.
Disease-free period of more than 5 years from prior malignancies other than pancreas (except curatively treated basal cell carcinoma, squamous cell carcinoma of the skin, or carcinoma in situ of the cervix and ductal carcinoma in situ [DCIS] breast disease).
Adequate contraceptive regimen (including prescription oral contraceptives [birth control pills], contraceptive injections, intrauterine device [IUD], double-barrier method [spermicidal jelly or foam with condoms or diaphragm], contraceptive patch, or surgical sterilization) before entry and throughout the study for female patients of reproductive potential or female partners of male patients.
Female patient with reproductive potential must have a negative urine beta human chorionic gonadotropin (bHCG) pregnancy test at Screening.
Willing to adhere to the prohibitions and restrictions specified in this protocol.
Patient must have signed an informed consent document.

You may not qualify if…

Patients with unresectable locally advanced disease without evidence of disease elsewhere.
Life expectancy of less than 12 weeks.
Uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled hypertension or seizure disorder.
Active infection not adequately responding to appropriate therapy.
Symptomatic or clinically evident ascites.
Serum sodium less than 130 mEq/L or conditions that may predispose patients to hyponatremia.
Female patients who are pregnant or lactating.
Male patients with female sexual partners who are unwilling to follow the strict contraception requirements described in this protocol.
Major surgery without full recovery or major surgery within 3 weeks of ON 01910.Na treatment start.
Evidence of brain metastases.
Any concurrent administration and/or prior administration within 4 weeks of the first dose of study drug, of radiotherapy, or immunotherapy.
Psychiatric illness/social situations that would limit the patient's ability to tolerate and/or comply with study requirements, or inability to comply with study and/or follow-up procedures (e.g., drug addition, chronic non-compliance, etc.).

Where it is running

UCSD Moores Cancer Center — La Jolla, California, United States
Desert Comprehensive Cancer Center — Palm Springs, California, United States
Pacific Cancer Care — Salinas, California, United States
Premiere Oncology — Santa Monica, California, United States
University of Colorado Cancer Center — Aurora, Colorado, United States
Kaiser Permanente Colorado — Denver, Colorado, United States
Poudre Valley Cancer Center of the Rockies — Fort Collins, Colorado, United States
Yale Cancer Center — New Haven, Connecticut, United States
Mount Sinai Comprehensive Cancer Center — Miami Beach, Florida, United States
University of Hawaii Cancer Center — Honolulu, Hawaii, United States
University of Kansas Cancer Center — Westwood, Kansas, United States
UMASS Medical School — Worcester, Massachusetts, United States
Karmanos Cancer Institute — Detroit, Michigan, United States
Billings Clinic Cancer Center — Billings, Montana, United States
Roswell Park Cancer Institute — Buffalo, New York, United States
New York University Langone Medical Center — New York, New York, United States
University of Rochester Medical Center — Rochester, New York, United States
University of North Carolina Lineberger Comprehensive Cancer Center — Chapel Hill, North Carolina, United States
Levine Cancer Institute — Charlotte, North Carolina, United States
Cone Health Cancer Center — Greensboro, North Carolina, United States
Hendersonville Hematology and Oncology at Pardee — Hendersonville, North Carolina, United States
Rex Cancer Center UNC Healthcare — Raleigh, North Carolina, United States
St. Alexis Medical Center-Mid Dakota Clinic PC — Bismarck, North Dakota, United States
University of Cincinnati Cancer Center — Cincinnati, Ohio, United States
Kaiser Permanente NW — Portland, Oregon, United States

Full record on ClinicalTrials.gov

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