Current partner codePEPTIDESDE
NCT00600886·Phase 3·INTERVENTIONAL

Safety and Efficacy of Pasireotide Long Acting Release (LAR) vs. Octreotide LAR in Patients With Active Acromegaly

Status

Completed

Phase

Phase 3

Enrollment

358

Locations

95

Results

Posted

Publications

3

Study summary

What the protocol is testing.

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

Treatment arms and agents.

DRUG

Pasireotide

Pasireotide LAR - intramuscular (i.m.) depot injection given once every 28 days.

DRUG

Octreotide

Octreotide LAR - i.m. depot injection given once every 28 days.

Timeline

From registration to results.

  1. First posted

    Jan 25, 2008

  2. Study start

    Feb 11, 2008

  3. Primary completion

    Mar 11, 2016

  4. Study completion

    Mar 11, 2016

  5. Results posted

    Jan 30, 2015

  6. Registry updated

    Jul 2, 2017

Outcomes

What the study measures.

Primary 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.

Secondary outcomes

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

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
ALL
Healthy volunteers
No

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

95 registered sites.

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

Related trials

More studies on Pasireotide.

Related PeptideStat pages

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