DRUG
Pasireotide
Pasireotide LAR - intramuscular (i.m.) depot injection given once every 28 days.
Status
Completed
Phase
Phase 3
Enrollment
358
Locations
95
Results
Posted
Publications
3
Study summary
The patients received either Pasireotide LAR or Octreotide LAR for one year of treatment. The objective of this study was to compare the proportion of patients with a reduction of mean GH level to \<2.5 µg/L and the normalization of IGF-1 to within normal limits (age and sex related) between the two treatment groups (pasireotide LAR and octreotide LAR) at 12 months. Following one year of treatment patients could proceed into the study extension. Patients who did not respond to the treatment they were randomized to (based on month 12 assessment results) were switched to the other treatment arm at month 13.
Interventions
DRUG
Pasireotide LAR - intramuscular (i.m.) depot injection given once every 28 days.
DRUG
Octreotide LAR - i.m. depot injection given once every 28 days.
Timeline
First posted
Jan 25, 2008
Study start
Feb 11, 2008
Primary completion
Mar 11, 2016
Study completion
Mar 11, 2016
Results posted
Jan 30, 2015
Registry updated
Jul 2, 2017
Outcomes
Percentage of Participants With a Reduction of Mean GH Level to <2.5 μg/L and the Normalization of IGF-1
Time frame · 12 months
Percentage of participants with a reduction of mean GH levels to \<2.5μg/L (based on a 5-point 2-hour profile) and normalization of sex- and age-adjusted IGF-1. Post surgery = patients with prior surgery but no previous medical treatment for acromegaly De novo = patients with de novo disease who refused pituitary surgery or for whom pituitary surgery was contraindicated.
Percentage of Participants With a Reduction of Mean GH Level to < 2.5μg/L
Time frame · 12 Months
Percentage of participants with a reduction of mean GH levels to \< 2.5μg/L (based on a 5-point 2-hour profile). Post surgery = patients with prior surgery but no previous medical treatment for acromegaly De novo = patients with de novo disease who refused pituitary surgery or for whom pituitary surgery was contraindicated.
Change From Baseline in Tumor Volume at 12 Months
Time frame · Baseline, 12 Months
Absolute and percentage change from baseline in tumor volume (assessed by pituitary MRI) Post surgery = patients with prior surgery but no previous medical treatment for acromegaly De novo = patients with de novo disease who refused pituitary surgery or for whom pituitary surgery was contraindicated.
Percentage of Participants With Normalization of IGF-1
Time frame · 12 Months
Percentage of participants with normalization of sex- and age-adjusted IGF-1. Post surgery = patients with prior surgery but no previous medical treatment for acromegaly De novo = patients with de novo disease who refused pituitary surgery or for whom pituitary surgery was contraindicated.
Percentage of Participants With a Reduction of Mean GH Level to < 2.5μg/L and Normalization of IGF-1
Time frame · Months 3, 6, 9, 12, 16, 19, 22, 25
Percentage of participants with a reduction of mean GH levels to \< 2.5μg/L (based on a 5-point 2-hour profile) and normalization of sex- and age-adjusted IGF-1. Denominator for time points up to Month 12 is the Full Analysis Set (FAS). Denominator for time points after Month 12 excludes patients who completed the core and did not enter the extension. Patients who discontinued were considered non-responders for the time points after discontinuation, patients who crossed over were considered non-responders for all time points after crossover. Analysis was based on data up to crossover (i.e., included data from both blinded core \& ext. phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included.)
Summary of Mean GH Values
Time frame · Baseline, Months 3, 6, 9, 12, 16, 19, 22, 25
Mean GH levels (based on a 5-point profile over 2 hours). Analysis was based on data up to crossover (i.e., included data from both blinded core and extension phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included).
Time to First Response for Patients Achieving a Reduction of Mean GH Level to < 2.5 μg/L and Normalization of IGF-1 (No. of Responders: Pasireotite LAR = 81, Octreotide LAR = 63) )
Time frame · Up to 26 months
Time to first response for patients achieving a reduction of mean GH level to \< 2.5 μg/L and normalization of IGF-1. Analysis was based on data up to crossover (i.e., included data from both blinded core and extension phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included).
Severity Scores of Acromegaly Symptoms
Time frame · Baseline, Months 12, 25
Severity scores of acromegaly symptoms (Headache, Fatigue, Perspiration, Paresthesias, Osteoarthralgia). Symptoms were scored from 0 (no symptom) to 4 (very severe). Analysis was based on data up to crossover (i.e., included data from both blinded core and extension phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included).
Ring Size
Time frame · Baseline, Months 12, 25
Ring size (based on jeweler's finger gauge). Analysis was based on data up to crossover (i.e., included data from both blinded core and extension phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included).
Health-related Quality-of-life as Measured by the AcroQoL Questionnaire
Time frame · Baseline, Months 12, 25
Acromegalyy quality of life (AcroQoL) total scores. The AcroQoL questionnaire is unidimensional and contains 22 items divided in two scales: one that evaluates physical aspects (eight items) and another one that evaluates psychological aspects (14 items). The scoring of the questionnaire was performed as specified by the instrument developers. Total scores range from 0 to 100. Higher scores represent better quality of life. Analysis was based on data up to crossover (i.e., included data from both blinded core and extension phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included).
Summary of Prolactin Levels
Time frame · Baseline, Months 12, 25
Prolactin Levels. Analysis was based on data up to crossover (i.e., included data from both blinded core and extension phase up to 26 Months for patients who continued the same treatment in the extension. For patients who switched to the other treatment, only data collected before crossover was included).
Eligibility
Inclusion criteria: * Patients with active acromegaly (based on elevated GH and IGF-1 levels) * Patients who have undergone one or more pituitary surgeries, but have not been treated medically, or de-novo patients presenting a visible pituitary adenoma on MRI and who refuse pituitary surgery or for whom pituitary surgery is contraindicated * Patients for whom written informed consent to participate in the study has been obtained prior to any study related activity Exclusion criteria: * Patients who are being or were treated with octreotide, lanreotide, dopamine agonists or GH antagonists with the exception of a single dose of short-acting octrotide or short-acting dopamine agonists. In case of a single dose of short-acting octrotide, the dose should not be used to predict the response to the octretide treatment. The single dose of short-acting octreotide or short-acting dopamine agonists should not be administered in the 3 days prior to randomization * Patients with compression of the optic chiasm causing any visual field defect * Patients who have received pituitary irradiation within the last ten years prior to visit 1 * Poorly controlled diabetic patients Other protocol-defined inclusion/exclusion criteria may apply
Study locations
Argentina · Belgium · Brazil · Canada · China · Colombia · Czechia · Denmark · France · Germany · Greece · Hungary · Israel · Italy · Mexico · Netherlands · Norway · Poland · Russia · South Korea · Spain · Sweden · Switzerland · Taiwan · Turkey (Türkiye) · United Kingdom · United States. Showing up to 24 locations stored in the fast local snapshot.
Cedars Sinai Medical Center The Pituitary Center
Los Angeles, California, United States
University of California at Los Angeles Division of Endocrinology
Los Angeles, California, United States
Stanford University Medical Center Stanford Cancer Center (3)
Stanford, California, United States
University of Florida SC
Gainesville, Florida, United States
Johns Hopkins University School of Medicine Dept.ofJohnsHopkinsUniv.
Baltimore, Maryland, United States
University of Michigan Comprehensive Cancer Center Deptof Endocrinology&Diabetes
Ann Arbor, Michigan, United States
Columbia University Medical Center- New York Presbyterian Dept. of CU Collegeof Phys&Sur
New York, New York, United States
Northport VA Medical Center CSOM230C2305
Northport, New York, United States
Oregon Health & Sciences University DeptofOregonHealth&Sciences(3)
Portland, Oregon, United States
Allegheny Endocrinology Associates
Pittsburgh, Pennsylvania, United States
University of Texas Southwestern Medical Center Danziger Research Bldg.
Dallas, Texas, United States
University of Texas/MD Anderson Cancer Center Regulatory -12
Houston, Texas, United States
Baylor College of Medicine
Houston, Texas, United States
Swedish Medical Center Dept.ofSeattle Neuroscience(2)
Seattle, Washington, United States
Novartis Investigative Site
CABA, Buenos Aires, Argentina
Novartis Investigative Site
Capital Federal, Buenos Aires, Argentina
Novartis Investigative Site
Buenos Aires, Argentina
Novartis Investigative Site
Brussels, Belgium
Novartis Investigative Site
Brussels, Belgium
Novartis Investigative Site
Ghent, Belgium
Novartis Investigative Site
Leuven, Belgium
Novartis Investigative Site
Fortaleza, Ceará, Brazil
Novartis Investigative Site
Brasília, Federal District, Brazil
Novartis Investigative Site
São Luís, Maranhão, Brazil
Publications
Related trials
Novartis · Somatostatin Receptor Positive (SSTR+) · Gastroenteropancreatic Neuroendocrine Tumor (GEP-NET)
Phase 3
Recruiting
240
2026-04
Memorial Sloan Kettering Cancer Center · Prolactin-Producing Pituitary Tumor
Phase 2
Recruiting
10
2026-03
RECORDATI GROUP · Pharmacokinetics · Safety
Phase 1
Completed
40
2026-02
Advanced Accelerator Applications · Gastro-enteropancreatic Neuroendocrine Tumor
Phase 3
Active, not recruiting
226
2026-01
Hospices Civils de Lyon · Enterostomy
Phase 2
Completed
57
2025-12
RECORDATI GROUP · Post-Bariatric Hypoglycemia
Phase 2
Active, not recruiting
93
2025-09
Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Acromegaly Due to Pituitary Adenoma · Acromegaly
Not applicable
Recruiting
120
2025-09
Sidney Kimmel Comprehensive Cancer Center at Thomas Jefferson University · Castrate Resistant Prostate Cancer · Chemotherapy Naive Prostate Cancer
Phase 2
Terminated
6
2025-04
Related PeptideStat pages
Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.