Efficacy and Safety of Pasireotide Administered Monthly in Patients With Cushing's Disease

Percentage of Patients Who Attain mUFC ≤1.0 x ULN or Have at Least 50 % Reduction From Baseline in mUFC

Controlled responder: mUFC ≤ 1.0×ULN. Partially controlled responder: at least 50% reduction in mUFC from Baseline, and mUFC \>1.0×ULN.

Time frame: M7, M12, M24, M36

Percentage of Patients Who Are Controlled Responders (mUFC ≤ 1.0 xULN) on at Least 4 of the 7 mUFC Assessments by Month 7 & on at Least 7 of the 12 mUFC Assessments by Month 12.

Percentage of patients with mUFC ≤ 1.0 x ULN at a minimum of 4 months up to and including Month 7, and at a minimum of 7 months up to and including Month 12 by randomized groups.

Time frame: Month 7, Month 12

Percentage of Patients With Uncontrolled Response at Month 7 & Month 12 Within the Subset of Patients Who Had Uncontrolled Response at a) Months 1 and 2; b) Months 1, 2, and 3

Percentage of patients with mUFC \> 1.0 xULN at Month 7 and Month 12 within the subset of patients who were uncontrolled at a) Months 1 \& 2, b) Months 1, 2, \& 3 by randomized groups.

Time frame: Month 7, Month12

Percent of Participants Attaining a mUFC ≤ 1.0 x ULN or at Least a 50% Reduction in mUFC From Baseline at Indicated Time Points

Time to first achievement of attaining a mUFC ≤ 1.0 x ULN or at least a 50% reduction in mUFC from baseline by randomized groups.

Time frame: Momth 7, Month 12

Percent of Participants Attaining a Duration of Controlled or Partially Controlled Response at Indicated Time Points

Duration of controlled or partially controlled response is defined as the period starting from the date of patient's first normalization (mUFC≤ 1.0 x ULN) or at least 50% reduction from baseline up to the date when the patient's mUFC \>1.0 x ULN and the reduction from baseline falls to less than 50% for the first time.

Time frame: Month 6, 12, 18

Percentage Change From Baseline on Plasma Adrenocorticotropic Hormone (ACTH) Over Time

Percentage change in ACTH (pmol/L) from Baseline by randomized groups.

Time frame: Months 7, 12, 24 & 36

Percentage Change From Baseline on Serum Cortisol Over Time

Percentage change in serum cortisol (nmol/L) from Baseline by randomized groups.

Time frame: Months 7, 12, 24 & 36

Actual Change From Baseline in Clinical Signs Over Time: Blood Pressure

Change in blood pressure measurements from Baseline

Time frame: Month 7

Actual Change From Baseline in Clinical Signs Over Time: Body Mass Index (BMI)

Change in BMI measurements from Baseline

Time frame: Month 7

Actual Change From Baseline in Clinical Signs Over Time: Weight

Change in weight measurements from Baseline

Time frame: Month 7

Actual Change From Baseline in Clinical Signs Over Time: Body Composition: Region

Change in body composition: region measurements from Baseline

Time frame: Month 7

Actual Change From Baseline in Clinical Signs Over Time: Waist Circumference

Change in waist circumference measurements from Baseline

Time frame: Month 7

Actual Change From Baseline in Clinical Signs Over Time: Cholesterol & Triglycerides

Change in parameter measurements: cholesterol \& triglycerides from Baseline

Time frame: Month 7

Percentage Change From Baseline in Clinical Signs Over Time

Percentage change in parameter measurements: blood pressure, body mass index, waist circumference, fasting serum lipid profile, weight, bone density and body composition (examined by DXA scan) from Baseline

Time frame: Month 7

Percentage of Participants Having a Favorable Shift From Baseline in Clinical Signs

This includes patients with improvements in symptoms from baseline. Clinical signs over time include: facial rubor, fat pads, hirsutism, striae, (via photographs by a second local physician who was blinded to the treatment dose and time point of the photograph) and muscle strength.

Time frame: Month 7

Percentage of Participants That Attained a Mean Urinary Free Cortisol (mUFC) <= 1.0 x Upper Limit of Normal (ULN) at Month 7 Regardless of Dose Up-titration at Month 4.

All of the participants who discontinued prior to month 4 evaluations were classed as non-responders. For participants missing month 7 mUFC assessments, the last available mUFC assessment at or after month 4 was carried forward as the month 7 mUFC assessment value. Analysis split by screening strata of mUFC Stratum 1: mUFC 1.5x to \< 2.0 x ULN Stratum 2: mUFC 2.0x to \<= 5.0 x ULN

Time frame: Month 7

Percentage of Patients That Attain a Reduction of at Least 50% in mUFC From Baseline

All of the participants who discontinued prior to month 4 evaluations were classed as non-responders. For participants missing month 7 mUFC assessments, the last available mUFC assessment at or after month 4 was carried forward as the month 7 mUFC assessment value. Analysis split by screening strata of mUFC Stratum 1:

Time frame: Months 7, 12, 24 & 36

Percent of Participants Attaining a Time to First Achievement of at Least a 50% Reduction in mUFC From Baseline at Indicated Time Points

Time to first achievement of a 5by randomized groups.0% reduction in mUFC from baseline

Time frame: every month in the core phase and every 3 months in the extension phase) up to and including the cut-off date for the Month 12 CSR (10-Nov-2015)

Percent of Participants With a Duration of at Least 50% Reduction in mUFC From Baseline at Indicated Time Points

Duration of 50% reduction from baseline is defined as the period starting from the date of patient's first 50% reduction from baseline

Time frame: Months 6, 12 & 18

Pharmacokinetic (PK) Parameter: Ctrough

Pasireotide trough levels (Ctrough) was 1 of the parameters used for PK assessments. Ctrough is the pre-dose PK concentration with an elapsed time from previous injection of 28+/-2 days. All patients randomized to the study had at least 1 PK observation \& were therefore included in the pharmacokinetic analysis set. PK observations with missing concentrations, missing dose, missing elapsed time or an elapsed time from previous injection outside of 28 ±2 days window were excluded. Given that SOM230 LAR was administered once a month, Ctrough was collected every 28 days and thus this provides a summary of Ctrough values provided by incident dose (last dose administered prior to PK sample collection), not by randomized dose, hence each column is equivalent to an incident dose \& not an arm/group. Patients randomized to either 10mg or 30mg could be titrated down to 5mg due to safety, or titrated up to 40mg, hence the 4 incident doses/columns that were allowed per protocol during this study.

Time frame: Days 29, 57, 85, 113, 141, 169, 197, 225, 253, 281, 309, 337

Pharmacokinetic (PK) Parameter: Cmax

Pasireotide peak levels (Cmax) was one of the parameters used for PK assessments. Cmax is the post-dose PK concentration with an elapsed time from the previous injection of 21+/-2 days. All patients randomized to the study had at least one PK observation and were therefore included in the pharmacokinetic analysis set (PAS). Cmax PK observations ("Day 20" and "Day 104") with an elapsed time from the previous injection outside of 21+/-2 days window were excluded. Given that SOM230 LAR was administered once a month, the Cmax were collected every 28 days in this study, thus this provides a summary of Cmax values provided by incident dose (last dose administered prior to PK sample collection), not by randomized dose, hence each column is equivalent to an incident dose and not an arm/group. Patients randomized to either the 10mg or 30mg could be titrated down to 5mg due to safety, or titrated up to 40mg, hence the 4 incident doses/columns that were allowed per protocol during this study.

Time frame: Days 22, 106, 190

Actual Change in Standardized Score of Cushing's Disease HRQoL (CushingQOL) Score From Baseline

CushingQol is a disease-specific patient-reported outcome instrument. It is a single-domain 12 item Cushing's disease quality of life instrument. The Cushing's syndrome quality of life (CushingQoL) questionnaire is a single domain questionnaire which includes 12 self-report items scored using a five point Likert scale anchored at (1=always/very much and 5=never/not at all). The patient is asked to report what they think or feel about their Cushing's syndrome and how much the illness has interfered in usual activities over the past 4 weeks. The total score is standardized on a 0-100 scale with lower scores indicating a greater impact on quality of life.

Time frame: Months 7, 12, 24 & 36

Actual Change in SF-12v2 Score From Baseline - Mental Component Summary

SF-12v2 General Health Survey is a general patient reported outcome instrument over time. It is scored to provide eight health domain scores (Bodily Pain (BP), General Health (GH), Physical Functioning (PF), Role-Physical (RP), Social Functioning (SF), Role-Emotional (RE), Vitality (VT) and Mental Health (MH)). These eight domain scores can be combined to form two summary scores reflecting overall physical and mental health: the Physical Component Summary (PCS) and the Mental Component Summary (MCS). The analyses reported here focus on PCS and MCS scores. The domain scores use a norm-based score, which standardizes the scores with respect to the mean and standard deviation of a nationally representative sample of United States (US) adults. These are the scores on the original scale which have not been transformed in any way. The possible range of scores is 0 to 100, with higher scores representing better outcomes.

Time frame: Months 7, 12 & 24

Actual Change in SF-12v2 Score From Baseline - Physical Component Summary

SF-12v2 General Health Survey is a general patient reported outcome instrument over time. It is scored to provide eight health domain scores (Bodily Pain (BP), General Health (GH), Physical Functioning (PF), Role-Physical (RP), Social Functioning (SF), Role-Emotional (RE), Vitality (VT) and Mental Health (MH)). These eight domain scores can be combined to form two summary scores reflecting overall physical and mental health: the Physical Component Summary (PCS) and the Mental Component Summary (MCS). The analyses reported here focus on PCS and MCS scores. The domain scores use a norm-based score, which standardizes the scores with respect to the mean and standard deviation of a nationally representative sample of United States (US) adults. These are the scores on the original scale which have not been transformed in any way. The possible range of scores is 0 to 100, with higher scores representing better outcomes.

Time frame: Months 7, 12 & 24