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Completed Phase 2 Interventional

A Study to Examine the Long Term Effect of Pramlintide on Body Weight and Its Safety and Tolerability in Obese Subjects

ClinicalTrials.gov ID: NCT00189514

Public ClinicalTrials.gov record NCT00189514. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 3, 2026, 1:29 AM EST

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Extension Study of Protocol 137OB-201 to Examine the Long Term Effect of Pramlintide on Body Weight and Its Safety and Tolerability in Obese Subjects

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a long term extension to study 137OB-201 which is designed to examine the effect of pramlintide on body weight and its safety and tolerability in obese subjects.

Study identification

NCT ID
NCT00189514
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
210 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2005 (Type not available)
Primary completion
Jun 2007 (Actual)
Completion
Jun 2007 (Actual)
Last update posted
Jun 11, 2015

2005 – 2007

United States locations

U.S. sites
21
U.S. states
18
U.S. cities
21
Facility City State ZIP Site status
Research Site Chula Vista California — —
Research Site San Diego California — —
Research Site Walnut Creek California — —
Research Site Miami Florida — —
Research Site Augusta Georgia — —
Research Site Chicago Illinois — —
Research Site Indianapolis Indiana — —
Research Site Overland Park Kansas — —
Research Site Baton Rouge Louisiana — —
Research Site Detroit Michigan — —
Research Site Edina Minnesota — —
Research Site St Louis Missouri — —
Research Site Butte Montana — —
Research Site New York New York — —
Research Site Cincinnati Ohio — —
Research Site Portland Oregon — —
Research Site Philadelphia Pennsylvania — —
Research Site Austin Texas — —
Research Site San Antonio Texas — —
Research Site Salt Lake City Utah — —
Research Site Olympia Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00189514, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 11, 2015 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00189514 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →