Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00772005 · ClinicalTrials.gov registry record · Phase 2

Study to Evaluate the Efficacy and Safety of Armodafinil as Adjunctive Therapy in Adults With Schizophrenia

A Phase 2 study of Schizophrenia, sponsored by Cephalon.

Completed
Registry status
Phase 2
Development phase
287
Enrollment target
20
Study locations

NCT00772005: Completed Phase 2 study of Schizophrenia, sponsored by Cephalon.

NCT00772005 is a Phase 2 study of Schizophrenia that has completed, run by Cephalon. The registered enrollment target is 287 participants, above the 218-participant average among 315 other Schizophrenia trials with a reported enrollment target (32% higher). The trial reports 20 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00772005, a Phase 2 study of Schizophrenia, has completed, sponsored by Cephalon.

COMPLETED
Registry status
Phase 2
Development phase
287 participants
Enrollment target
20
Study locations

Study Summary

The primary objective of the study is to evaluate whether armodafinil treatment is more effective than placebo as adjunctive therapy to antipsychotic medication in alleviating the negative symptoms of schizophrenia

Primary Outcome

PANSS rates severity of psychopathology in schizophrenics. 7 items measure NEGATIVE symptoms: blunted affect, social withdrawal, poor rapport, passive/apathetic social withdrawal, difficulty in abstract thinking, lack of spontaneity and flow of conversation, stereotyped thinking. Each item is scored on a 7-point severity scale: 1=absent, 2=minimal, 3=mild, 4=moderate, 5=moderate severe, 6=severe, 7=extreme. Negative Scale score ranges from 7-49 (higher more severe). Data represents change in Neg

Conditions Studied

Interventions

  • DRUG placebo
  • DRUG armodafinil

Study Locations (20)

California

  • Omega Clinical Trials - Anaheim
  • Synergy Clinical Research Center - Escondido
  • Collaborative NeuroScience - Garden Grove
  • Excell Research - Oceanside
  • CNRI Los Angeles LLC - Pico Rivera
  • CNRI-San Diego LLC - San Diego
  • Neuropsychiatric Research Center of Orange County - Santa Ana
  • Collaborative NeuroScience Network - Torrance

Florida

  • Scientific Clinical Research, Inc. - Aventura
  • Mental Health Advocates. Inc - Boca Raton
  • Fidelity Clinical Research - Lauderhill
  • Stedman Clinical Trials, LLC - Tampa

Georgia

  • Atlanta Center for Medical Research - Atlanta
  • Comprehensive Neuroscience Inc - Atlanta
  • Carman Research - Smyrna

Connecticut

  • The Hospital of Central Connecticut - New Britain
  • Yale University School of Medicine - New Haven

Arkansas

  • K and S Professional Research Services, LLC - Little Rock

Illinois

  • Uptown Research Institute. LLC - Chicago

Kansas

  • Via Christi Research - Wichita

Trial Details

FieldValue
Enrollment Target 287 participants
Start Date 2008-09
Est. Completion 2010-05
Phase Phase 2
Cephalon

64 total trials

What the finished NCT00772005 record still lists

NCT00772005 is an interventional study that assigns participants to a tested intervention. The registered 287 participants enrollment target is mid-sized for trials with a published cap, above the 218-participant average among 315 other Schizophrenia trials with a reported enrollment target (32% higher).

The record links to 1 condition, with Schizophrenia appearing as the primary indexed condition, and to 2 interventions - of which placebo is the first listed.

NCT00772005 names 20 study sites across 7 states, led by California, Florida, Georgia.

Frequently Asked Questions

What is clinical trial NCT00772005 about?

NCT00772005 is a clinical study titled "Study to Evaluate the Efficacy and Safety of Armodafinil as Adjunctive Therapy in Adults With Schizophrenia". The primary objective of the study is to evaluate whether armodafinil treatment is more effective than placebo as adjunctive therapy to antipsychotic medication in alleviating the negative symptoms of schizophrenia

What is the current status of trial NCT00772005?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 287 participants. The study started on 2008-09. Estimated completion is 2010-05.

What conditions does trial NCT00772005 study?

This clinical trial studies the following conditions: Schizophrenia.

What interventions are being tested in trial NCT00772005?

The interventions under investigation include: placebo (DRUG), armodafinil (DRUG).

Who is sponsoring clinical trial NCT00772005?

This trial is sponsored by Cephalon, which has 64 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00772005 being conducted?

This trial has 20 study locations across Arkansas, California, Connecticut, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Schizophrenia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00772005's enrollment target sits among peer trials

287 65th of 315 higher than 251 of 315 other Schizophrenia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Schizophrenia 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03094429 · 287 participants · Phase 2

    An Adaptive Phase II/III, Two-Part, Double-Blind, Randomized, Placebo-controlled, Dose-Finding, Multi-center Study of the Safety and Efficacy of NaBen®, as an Add-on Therapy With Clozapine, for Residual Symptoms of Refractory Schizophrenia in Adults

  • NCT06385080 · 287 participants · Phase 1

    A Study of Amivantamab Alone or in Addition to Other Treatment Agents in Participants With Head and Neck Cancer

  • NCT06919224 · 287 participants · NA

    Delivering Patient-Facing Evidence-Based Guidelines Through mHealth to Adults With Sickle Cell Disease

  • NCT02098265 · 288 participants · NA

    A Closed Loop Neural Activity Triggered Stroke Rehabilitation Device

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00772005, the US trial registry maintained by the National Library of Medicine. NCT00772005 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.