Long Term Study With B2036-PEG

NCT ID: NCT00143416

Last Updated: 2008-07-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-04-30

Study Completion Date

2007-07-31

Brief Summary

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Primary objective: To investigate the efficacy and safety of Pegvisomant in Japanese patients with acromegaly.

Detailed Description

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Conditions

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Acromegaly

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Pegvisomant

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patients with acromegaly who have received at least one dose of B2036-PEG in the preceding study (A6291009).

Exclusion Criteria

* Switching to other therapeutic methods for acromegaly
Minimum Eligible Age

20 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Kobe, Hyogo PREF, Japan

Site Status

Pfizer Investigational Site

Kozukue-cho, Kouhoku-ku, Yokohama-shi, Kanagawa, Japan

Site Status

Pfizer Investigational Site

Kyoto, Kyoto, Japan

Site Status

Pfizer Investigational Site

Hamamatsu, Shizuoka, Japan

Site Status

Pfizer Investigational Site

Bonkyo-ku, Tokyo, Japan

Site Status

Pfizer Investigational Site

Shinjuku-ku, Tokyo, Japan

Site Status

Pfizer Investigational Site

Gakuhara, Kishiwada, Osaka, , Japan

Site Status

Pfizer Investigational Site

Sannomaru-cho, Naka-ku, Nagoya-shi, , Japan

Site Status

Countries

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Japan

Related Links

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Other Identifiers

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A6291011

Identifier Type: -

Identifier Source: org_study_id