Pasireotide LAR Therapy of Silent Corticotroph Pituitary Tumors

Exclusion Criteria

• •1. Patients with Cushing's disease (biochemical evidence of hypercortisolism)
• •2. Patients with compression of the optic chiasm causing any visual field defect that requires surgical intervention
• •3. Diabetic patients with poor glycemic control as evidenced by HbA1c \>8%
• •4. Patients who are hypothyroid or adrenally insufficient and not on adequate replacement therapy
• •5. Patients with symptomatic cholelithiasis and acute or chronic pancreatitis
• •6. Patients with risk factors for torsade de pointes, i.e., patients with a baseline QTcF (Fridericia's Correction Formula value) \>450 ms in males, and \>460 ms in females
• •7. Hypokalaemia, hypomagnesaemia, uncontrolled hypothyroidism, family history of long QT syndrome or concomitant medications with known risk of Torsades de pointes (TdP). Drugs with possible risk of TdP should be avoided whenever feasible
• •8. Patients who have congestive heart failure (NYHA Class III or IV), unstable angina, sustained ventricular tachycardia, clinically significant bradycardia, advanced heart block, history of acute myocardial infarction (MI) less than one year prior to study entry or clinically significant impairment in cardiovascular function
• •9. Concomitant disease(s) that could prolong the QT interval such as autonomic neuropathy (caused by diabetes or Parkinson's disease), HIV, cirrhosis, uncontrolled hypothyroidism or cardiac failure
• •10. Patients with liver disease such as cirrhosis, chronic active hepatitis, or chronic persistent hepatitis, or patients with alanine aminotransferase (ALT)/aspartate aminotransferase (AST) \> 2.0 X upper limit of normal (ULN), serum bilirubin \>2.0 X ULN
• •11. Presence of Hepatitis B surface antigen (HbsAg) or Hepatitis C antibody test (anti-HCV)
• •12. Patients with serum creatinine \>2.0 X ULN
• •13. Patients with white blood cell (WBC) count \<3 X 109/L; Hb 90% \< lower limit of normal (LLN); platelet (PLT) count \<100 X 109/L
• •14. Patients with the presence of active or suspected acute or chronic uncontrolled infection
• •15. Patients who have undergone major surgery/surgical therapy for any cause within 4 weeks prior screening
• •16. Patients with abnormal coagulation (PT and/or activated partial thromboplastin time (APTT) elevated by 30% above normal limits) or patients receiving anticoagulants that affect PT (prothrombin time) or APTT (activated partial thromboplastin time)
• •17. History of syncope or family history of idiopathic sudden death
• •18. History of immunocompromise, including a positive HIV test result (ELISA and Western blot)
• •19. Sexually active males unless they use a condom during intercourse while taking drug and for 3 months following last dose of pasireotide and should not father a child in this period. A condom is required to be used also by vasectomized men in order to prevent delivery of the drug via seminal fluid
• •20. Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive urine pregnancy test
• •21. Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during dosing and 3 months following last dose of pasireotide. Highly effective contraception methods include:
• •* Total abstinence when this is in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception
• •* Female sterilization (have had surgical bilateral oophorectomy with or without hysterectomy) or tubal ligation at least six weeks before taking study treatment. In case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment
• •* Male sterilization (at least 6 months prior to screening). For female subjects on the study the vasectomized male partner should be the sole partner for that subject
• •* Combination of any two of the following (a+b or a+c, or b+c):
• •1. Use of oral, injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate \<1%), for example hormone vaginal ring or transdermal hormone contraception.
• •2. Placement of an intrauterine device (IUD) or intrauterine system (IUS)
• •3. Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/vaginal suppository
• •* In case of use of oral contraception women should have been stable on the same pill for a minimum of 3 months before taking study treatment.
• •* Women are considered post-menopausal and not of child bearing potential if they have had 12 months of natural (spontaneous) amenorrhea with an appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms) or have had surgical bilateral oophorectomy (with or without hysterectomy) or tubal ligation at least six weeks ago. In the case of oophorectomy alone, only when the reproductive status of the woman has been confirmed by follow up hormone level assessment is she considered not of child bearing potential.