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NCT01656577 · ClinicalTrials.gov registry record · Early Phase 1

Pexacerfont for Stress-induced Food Craving

A Early Phase 1 study, sponsored by National Institute on Drug Abuse (NIDA).

Terminated
Registry status
Early Phase 1
Development phase
31
Enrollment target

NCT01656577: Clinical Trial Early Phase 1 study, sponsored by National Institute on Drug Abuse (NIDA).

NCT01656577 is a Early Phase 1 study that was terminated before completion, run by National Institute on Drug Abuse (NIDA). The registered enrollment target is 31 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01656577, a Early Phase 1 study, was terminated before completion, sponsored by National Institute on Drug Abuse (NIDA).

TERMINATED
Registry status
Early Phase 1
Development phase
31 participants
Enrollment target

Study Summary

Background: \- Stress can cause people to give in to temptations to eat less healthily. People who are on weight loss diets often have problems sticking to their diets when they are stressed. Some tests have shown that the drug pexacerfont can help reduce stress-related seeking of high-calorie foods. However, it has not been tested on reducing food craving. Researchers want to test pexacerfont on people who are on diets to see if it can reduce stress-related food cravings. Objectives: \- To see if pexacerfont can help reduce stress-induced food cravings. Eligibility: \- Individuals between 21 and 65 years of age who are on a diet to control their weight. Design: * Participants will be screened with a physical exam and medical history. This study requires seven visits over about 35 days. * Participants will take either pexacerfont or placebo pills during the study. They will have three pills every morning. They will record video of themselves taking the pills every day. * Every evening, participants will fill out a questionnaire. It will ask questions about feelings and behaviors related to eating and food craving. * Participants will have regular study visits while taking the pills. The visits will involve questions about stressful situations and food cravings. One visit will involve a mildly stressful math test, followed by tasting of different foods. This test will look at whether pexacerfont can affect food preferences. Participants will provide blood and saliva samples as directed at these study visits. * Participants will have follow-up phone calls 1, 3, and 6 months after the end of the study.

Interventions

  • DRUG Pexacerfont

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2012-06
Est. Completion 2015-09
Phase Early Phase 1

Why NCT01656577 stopped before completion

NCT01656577 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 1 intervention - of which Pexacerfont is the first listed.

NCT01656577 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01656577 about?

NCT01656577 is a clinical study titled "Pexacerfont for Stress-induced Food Craving". Background: \- Stress can cause people to give in to temptations to eat less healthily. People who are on weight loss diets often have problems sticking to their diets when they are stressed. Some tests have shown that the drug pexacerfont can help reduce stress-related seeking of high-calorie food...

What is the current status of trial NCT01656577?

This trial is currently terminated. It is a Early Phase 1 study. The enrollment target is 31 participants. The study started on 2012-06. Estimated completion is 2015-09.

What interventions are being tested in trial NCT01656577?

The interventions under investigation include: Pexacerfont (DRUG).

Who is sponsoring clinical trial NCT01656577?

This trial is sponsored by National Institute on Drug Abuse (NIDA), which has 335 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01656577's enrollment target sits among peer trials

31 794th of 2000 higher than 1,194 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01656577, the US trial registry maintained by the National Library of Medicine. NCT01656577 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.