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NCT00489294

An Open-Label Study of the Pharmacokinetics and Pharmacodynamics of Syntropin (a Human Growth Hormone) in Growth Hormone-Suppressed Healthy Volunteers

Completed Phase 1 Last updated 9 March 2012
What this trial tests

Phase 1 trial testing Syntropin in Growth Hormone Deficiency in 20 participants. Completed in 1 June 2005.

Timeline
1 August 2004
Primary endpoint
1 June 2005
1 June 2005

Quick facts

Lead sponsorPhage Pharmaceuticals, Inc.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment20
Start date1 August 2004
Primary completion1 June 2005
Estimated completion1 June 2005
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Phage Pharmaceuticals, Inc. — full company profile →

Who can join

Adults 18 to 45, any sex, with Growth Hormone Deficiency. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to evaluate the pharmacokinetics of Syntropin (a human growth hormone) and to determine the serum concentration of IGF-1 after Syntropin injection.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Growth Hormone Deficiency

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00489294.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing