Synthetic Human Secretin in Children With Autism and Gastrointestinal Dysfunction

NCT ID: NCT00036231

Last Updated: 2005-11-21

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

TERMINATED

Clinical Phase

PHASE3

Study Classification

INTERVENTIONAL

Study Start Date

2002-04-30

Brief Summary

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The purpose of the study is to determine the effect of multiple doses of secretin on autism.

Detailed Description

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Conditions

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Autism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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RG1068 (Synthetic Human Secretin)

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Autism
* Gastrointestinal dysfunction
Minimum Eligible Age

32 Months

Maximum Eligible Age

59 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Repligen Corporation

INDUSTRY

Sponsor Role lead

Countries

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United States

Related Links

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Other Identifiers

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RG1068-03

Identifier Type: -

Identifier Source: org_study_id