Extension Study of the Safety and Efficacy of Atiprimod Treatment in Neuroendocrine Carcinoma

Completed · Phase 2

Conditions studied: Neuroendocrine Carcinoma

In brief

This study is an extension study to the Callisto protocol CP-106. Subjects must have completed all 12 treatment cycles of CP-106 without disease progression as per RECIST criteria,to be eligible to to be enrolled in this study. This study will evaluate the safety and efficacy of atiprimod treatment in patients with low to intermediate grade neuroendocrine carcinoma who have metastatic or unresectable local-regional cancer and who have either symptoms (diarrhea, flushing and/or wheezing) despite standard therapy (octreotide) or progression of neuroendocrine tumor(s).

Key facts

Study ID

NCT00663429

Run by

Callisto Pharmaceuticals

People needed

10

Starts

2007-11-01

Expected to finish

2010-03-01

Last updated by the study team

2011-08-31

Who can join

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

You may qualify if…

• Subject was enrolled in Protocol No. CP-106 and successfully completed 12 treatment cycles.
• Subject must have been classified as a responder at the time of completion of Protocol No. CP-106 [i.e., SD or better per RECIST Committee criteria or stable symptoms or better (defined as an average daily frequency of bowel movements, flushing episodes and/or wheezing episodes that is the same as or less than the average daily frequency of bowel movements, flushing episodes and/or wheezing episodes recorded during the 14-day screening period prior to enrollment in Protocol No. CP-106)].
• Subject must understand and voluntarily sign the informed consent document.
• Subject must have adequate organ function defined as follows: Absolute granulocyte count (AGC) >1,500/mm3, hemoglobin >8 g/dl, platelets >100,000/mm3, serum bilirubin <1.5 x upper limit of normal (ULN), serum creatinine <1.5 mg/dL, SGOT ≤Grade 1 per NCI CTCAE, SGPT ≤Grade 1 per NCI CTCAE.
• Women of child bearing potential (WCBP) must have a negative serum or urine pregnancy test. In addition sexually active WCBP must agree to use adequate contraceptive methods (oral, injectable or implantable hormonal contraceptive; tubal ligation; intra-uterine devices; barrier contraceptive with spermicide; or vasectomized partner).

You may not qualify if…

• Subject who was enrolled in Protocol No. CP-106 and who did not successfully complete 12 treatment cycles.
• If WCBP, pregnant, lactating or not using adequate contraception.
• Clinically relevant active infection or serious co-morbid medical conditions that are uncontrolled or whose control may be jeopardized by atiprimod treatment.
• Psychiatric disorders rendering subjects incapable of complying with the requirements of the protocol.
• Any condition which, in the opinion of the Investigator, places the subject at unacceptable risk if he/she were to participate in the study.
• As atiprimod is a potent inhibitor of CYP2D6, the use of drugs that are substrates of CYP2D6 (e.g. beta blockers, antidepressants, and antipsychotic;) will not be allowed while on study.

Where it is running

• Hematology Oncology Services of Arkansas — Little Rock, Arkansas, United States
• Mount Sinai Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

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