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NCT00264732 · ClinicalTrials.gov registry record · Phase 2

A Study of Amolimogene (ZYC101a) in Patients With High Grade Cervical Intraepithelial Lesions of the Uterine Cervix

A Phase 2 study of Uterine Cervical Dysplasia, sponsored by Eisai.

Completed
Registry status
Phase 2
Development phase
251
Enrollment target
20
Study locations

NCT00264732: Completed Phase 2 study of Uterine Cervical Dysplasia, sponsored by Eisai.

NCT00264732 is a Phase 2 study of Uterine Cervical Dysplasia that has completed, run by Eisai. The registered enrollment target is 251 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% higher). The trial reports 20 study locations across 13 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00264732, a Phase 2 study of Uterine Cervical Dysplasia, has completed, sponsored by Eisai.

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

Study Summary

The purpose of this study is to evaluate the efficacy and safety of amolimogene, in the treatment of patients with high-grade cervical intraepithelial lesions of the uterine cervix.

Conditions Studied

Interventions

  • OTHER Placebo
  • DRUG Amolimogene

Study Locations (20)

Florida

  • Visions Clinical Research - Boynton Beach
  • University of Florida, Miami - Miami
  • Physician Care Clinical Research - Sarasota
  • Insignia Clinical Research - Tampa
  • Comprehensive Clinical Trials LLC - West Palm Beach

California

  • Arrowhead Regional Medical Center - Colton
  • The Center for Advanced Research and Education, Inc. - Palm Springs
  • Medical Center for Clinical Research - San Diego

Arizona

  • Arizona Wellness Center for Women/Precision Trials, LLC - Phoenix
  • University of Arizona - Tucson

Alabama

  • University of Alabama - Birmingham

Colorado

  • Physicians Research Options, LC - Lakewood

Georgia

  • Medical College of Georgia, Department of Family Medicine - Augusta

Idaho

  • Rosemark Women's Care Specialists - Idaho Falls

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 251 participants
Start Date 2005-07
Est. Completion 2009-05
Phase Phase 2
Eisai

287 total trials

What the finished NCT00264732 record still lists

NCT00264732 is an interventional study that assigns participants to a tested intervention. The registered 251 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (89% higher).

The record links to 1 condition, with Uterine Cervical Dysplasia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00264732 names 20 study sites across 13 states, led by Florida, California, Arizona.

Frequently Asked Questions

What is clinical trial NCT00264732 about?

NCT00264732 is a clinical study titled "A Study of Amolimogene (ZYC101a) in Patients With High Grade Cervical Intraepithelial Lesions of the Uterine Cervix". The purpose of this study is to evaluate the efficacy and safety of amolimogene, in the treatment of patients with high-grade cervical intraepithelial lesions of the uterine cervix.

What is the current status of trial NCT00264732?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 251 participants. The study started on 2005-07. Estimated completion is 2009-05.

What conditions does trial NCT00264732 study?

This clinical trial studies the following conditions: Uterine Cervical Dysplasia.

What interventions are being tested in trial NCT00264732?

The interventions under investigation include: Placebo (OTHER), Amolimogene (DRUG).

Who is sponsoring clinical trial NCT00264732?

This trial is sponsored by Eisai, which has 287 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00264732 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Uterine Cervical Dysplasia

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 NCT00264732's enrollment target sits among peer trials

251 222nd of 2000 higher than 1,779 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00264732, the US trial registry maintained by the National Library of Medicine. NCT00264732 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.