Long-term Safety and Efficacy Study of Octreotide Implant in Patients With Acromegaly

NCT ID: NCT01295060

Last Updated: 2013-09-20

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE3
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-02-28
• Study Completion Date: 2012-06-30

Brief Summary

This is a long term study to evaluate the safety, tolerability and efficacy of an Octreotide Implant in patients that were previously treated with an Octreotide implant.

Detailed Description

Evaluation on the long-term safety and tolerability, including local tolerability of the implant site, of the 84-mg octreotide hydrogel implant in subjects with acromegaly who had been successfully treated with the 84-mg octreotide hydrogel implant in the Phase III study IP107-001.

Conditions

Acromegaly

Keywords

Acromegaly; Octreotide; IGF-1; Growth Hormone; Implant; Hydrogel

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Octreotide Implant

Group Type: EXPERIMENTAL

Octreotide

Intervention Type: DRUG

84 mg Octreotide Implant

Interventions

Octreotide

84 mg Octreotide Implant

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Currently enrolled in the Extension Phase of Study IP107-001 and received at least one 84-mg octreotide hydrogel implant prior to enrollment OR previously enrolled in the Extension Phase of Study IP107-001 and currently taking lanreotide or octreotide.
• Subjects who have been successfully treated with the 84-mg octreotide hydrogel implant in Study IP107 001.
• In the opinion of the Investigator; subject has no unstable chronic medical conditions and no clinically significant findings that would preclude subject's participation in the study.
• Subjects must be able to communicate, provide and sign written informed consent, and be willing to participate and comply with study requirements.

Exclusion Criteria

• Pituitary surgery less than 3 months prior to enrollment into this study
• Liver disease (eg, cirrhosis, chronic active or persistent hepatitis or persistent abnormalities of ALT, AST [level >2× normal] or direct bilirubin [level >1.5× normal])
• Unstable angina, sustained ventricular arrhythmias or heart failure (NYHA III and IV)
• Acute myocardial infarction within 3 months of Screening
• Uncontrolled diabetes defined as having an HbA1c ≥9%
• Symptomatic cholelithiasis
• History of drug or alcohol abuse
• Received any investigational drug or participated in another clinical trial except for study IP107 001 within 30 days of enrollment into this study
• Received radiotherapy for pituitary tumor or any radiotherapy above the neck at any time prior to enrollment into this study
• Receiving pegvisomant, dopamine agonist or other therapy in combination with somatostatin to control GH or IGF-1 levels prior to enrollment into this study
• History or presence of significant cardiovascular, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, psychiatric disease, any other severe coexisting or, terminal systemic disease that limits life expectancy, or may interfere with the conduct of the study, or subjects who are incarcerated in penal institutions or are committed to mental institutions
• Women who are pregnant or lactating. For females of childbearing potential, a positive pregnancy test prior to enrollment, or an unwillingness to use accepted forms of reliable birth control for study duration (including bilateral tubal ligation, use of oral contraceptives, double barrier methods [diaphragm with spermicidal gel or condoms with contraceptive foam], Depo-Provera®, hormonal implants, partner vasectomy, and total abstinence). Pregnancy tests are not required (indicate "n/a") for males, or for females not of childbearing potential (post-menopausal with last menstrual period >1 year ago or total hysterectomy with bilateral oophorectomy)
• An unwillingness on the part of a male subject to abstain from sexual intercourse with pregnant or lactating women or an unwillingness to use a condom and spermicide and another form of contraception (eg, IUD, birth control pills taken by female partner, diaphragm with spermicide) if engaging in sexual intercourse with a woman who could become pregnant until discharge from the study

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Endo Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Denver, Colorado, United States

Chicago, Illinois, United States

Baltimore, Maryland, United States

Cleveland, Ohio, United States

Portland, Oregon, United States

Seattle, Washington, United States

Countries

United States

Other Identifiers

EN3332-301

Identifier Type: -

Identifier Source: org_study_id