Quarfloxin in Patients With Low to Intermediate Grade Neuroendocrine Carcinoma

Completed · Phase 2

Conditions studied: Neuroendocrine Tumors, Carcinoid Tumor

In brief

This is a Phase 2, open-label, multicenter, efficacy and safety study of quarfloxin in patients with low or intermediate grade neuroendocrine cancer. The purpose of this study is to evaluate the rate of clinical benefit response to quarfloxin treatment including the reduction in secretory symptoms of flushing and/or diarrhea or the reduction quantifiable hormones or other biochemical tumor markers.

Key facts

Study ID

NCT00780663

Run by

Cylene Pharmaceuticals

People needed

25

Starts

2008-10-01

Expected to finish

2010-03-01

Last updated by the study team

2011-06-15

Who can join

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

You may qualify if…

• Histologically or cytologically confirmed low or intermediate grade neuroendocrine carcinoma including carcinoid and islet cell cancer. Patients with neuroendocrine tumors associated with MEN1 syndrome are eligible.
• Measureable disease by RECIST
• Unresectable or metastatic disease
• Secretory symptoms of diarrhea or flushing or both attributed to their carcinoid tumor and/or quantifiable hormones or other biochemical markers
• Males and females 18 years of age or older.
• Zero to two prior cytotoxic chemotherapy regimens.
• Patients may be receiving concomitant octreotide Sandostatin®
• Patients must have central IV access, or agree to the insertion of a central IV line.
• All previous cancer therapies, radiation, and surgery, must have been discontinued at least 21 days prior to the start of treatment.
• Acceptable liver function
• Acceptable renal function
• Acceptable hematologic status
• ECOG Performance Status ≤1.
• Anticipated survival of at least 6 months.
• Able to maintain a patient diary.
• For men and women of child-producing potential, use of effective contraceptive methods during the study and for one month after discontinuation of treatment.
• Ability to understand the requirements of the study, provide written informed consent and agree to abide by the study restrictions and return to the clinic for required assessments.

You may not qualify if…

• Poorly differentiated neuroendocrine carcinoma, high-grade neuroendocrine carcinoma, adenocarcinoid, goblet cell carcinoid or small cell carcinoma.
• Pregnant or nursing women.
• Severe chronic obstructive pulmonary disease with hypoxemia or an uncorrectable pulmonary compromise.
• Seizures not controlled by anticonvulsant therapy.
• Participation in any investigational drug study within 28 days before quarfloxin administration or currently receiving investigational therapy.
• Patients with a second malignancy requiring active treatment.
• Active symptomatic bacterial, fungal, or viral infection including active HIV or viral hepatitis.
• Prior treatment with quarfloxin.
• Clinically significant bleeding event within the last 3 months, unrelated to trauma, or underlying condition that would be expected to result in a bleeding diathesis.
• Patients who have exhibited allergic reactions to a similar structural compound or formulation.
• Any illness or condition that in the opinion of the investigator may affect safety of treatment or evaluation of any of the study's endpoints.

Where it is running

• Birmingham Hematology and Oncology — Birmingham, Alabama, United States
• Rocky Mountain Cancer Centers — Denver, Colorado, United States
• Front Range Cancer Specialists — Fort Collins, Colorado, United States
• Study site — Ocala, Florida, United States
• Southern New Mexico Cancer Center — Las Cruces, New Mexico, United States
• Texas Oncology — Amarillo, Texas, United States
• Texas Oncology — Dallas, Texas, United States
• El Paso Cancer Treatment Center — El Paso, Texas, United States
• Cancer Care Centers of South Texas — Kerrville, Texas, United States
• UT Health Science Center — San Antonio, Texas, United States
• Tyler Cancer Center — Tyler, Texas, United States
• Virginia Mason Medical Center — Seattle, Washington, United States
• Northwest Cancer Specialists — Vancouver, Washington, United States

Full record on ClinicalTrials.gov

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