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Completed Phase 2 Interventional

ALK37-005: A Study of ALKS 37 (RDC-1036) in Adults With Opioid-induced Constipation (OIC)

ClinicalTrials.gov ID: NCT01382797

Public ClinicalTrials.gov record NCT01382797. 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 Oct 27, 2026, 12:05 PM 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 Phase 2b Randomized, Double-blind, Placebo-controlled, Repeat-dose Study to Evaluate the Safety, Tolerability, and Efficacy of ALKS 37 in Subjects With Opioid-induced Constipation

Brief summary

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

The purpose of this study is to evaluate the safety, tolerability and efficacy of ALKS 37 when administered daily for 4 weeks to adults with Opioid-induced Constipation (OIC).

Study identification

NCT ID
NCT01382797
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alkermes, Inc.
Industry
Enrollment
157 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Aug 2011 (Type not available)
Primary completion
Apr 2012 (Actual)
Completion
Apr 2012 (Actual)
Last update posted
Jun 13, 2012

2011 – 2012

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Alkermes Study Site Mesa Arizona 85206 —
Alkermes Study Site Phoenix Arizona 85053 —
Alkermes Study Site National City California 91950 —
Alkermes Study Site Oceanside California 92056 —
Alkermes Study Site Pasadena California 91105 —
Alkermes Study Site Denver Colorado 80211 —
Alkermes Investigational Site DeLand Florida 32724 —
Alkermes Study Site Ormond Beach Florida 32174 —
Alkermes Study Site St. Petersburg Florida 33709 —
Alkermes Study Site Stockbridge Georgia 30281 —
Alkermes Study Site Boise Idaho 83704 —
Alkermes Study Site New Orleans Louisiana 70114 —
Alkermes Study Site Kalamazoo Michigan 49009 —
Alkermes Study Site Las Vegas Nevada 89144 —
Alkermes Study Site Belvidere New Jersey 07823 —
Alkermes Study Site Brooklyn New York 11218 —
Alkermes Study Site Cincinnati Ohio 45224 —
Alkermes Study Site Oklahoma City Oklahoma 73134 —
Alkermes Study Site Medford Oregon 97504 —
Alkermes Study Site San Antonio Texas 78228 —

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 NCT01382797, 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 13, 2012 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01382797 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →