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Completed Phase 2 Interventional

A Study of Nasal PYY3-36 and Placebo for Weight Loss in Obese Subjects

ClinicalTrials.gov ID: NCT00537420

Public ClinicalTrials.gov record NCT00537420. 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 Jul 23, 2026, 10:51 AM EDT

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

Official title

A 24-Week, Blinded, Randomized, Placebo-Controlled Dose-Ranging Trial of Nasal PYY3-36 for Weight Loss in Healthy Obese Patients

Study identification

NCT ID
NCT00537420
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Nastech Pharmaceutical Company, Inc.
Industry
Enrollment
551 participants

Conditions and interventions

Conditions

Interventions

  • Nasal Placebo Drug
  • Placebo Capsule Drug
  • PYY3-36 Drug
  • Sibutramine Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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 30, 2007
Primary completion
Jun 30, 2008
Completion
Aug 31, 2008
Last update posted
Sep 14, 2008

2007 – 2008

United States locations

U.S. sites
29
U.S. states
15
U.S. cities
28
Facility City State ZIP Site status
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Peoria Arizona 85381
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Phoenix Arizona 85050
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Anaheim California 92801
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Beverly Hills California 90211
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Carmichael California 95608
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Orange California 92869
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Sacramento California 95816
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 San Diego California 92108
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 San Diego California 92130
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 San Francisco California 94102
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Pembroke Pines Florida 33024
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Atlanta Georgia 30328
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Augusta Georgia 30909
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Evansville Indiana 47713
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Valparaiso Indiana 46383
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Baton Rouge Louisiana 70808
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Brooklyn Center Minnesota 55430
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Las Vegas Nevada 89104
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Manlius New York 13104
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Charlotte North Carolina 28209
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Raleigh North Carolina 27612
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Cleveland Ohio 44122
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Reading Pennsylvania 19606
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Greer South Carolina 29651
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Mt. Pleasant South Carolina 29464
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Austin Texas 78705
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 San Antonio Texas 78229-3894
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Temple Texas 76508
For additional information regarding investigative sites for this trial, contact 1-425-415-3011 Salt Lake City Utah 84049

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 NCT00537420, 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 Sep 14, 2008 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00537420 live on ClinicalTrials.gov.

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