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Completed Phase 2 Interventional

A Study of REOLYSIN® in Combination With Paclitaxel and Carboplatin in Patients With Squamous Cell Carcinoma of the Lung

ClinicalTrials.gov ID: NCT00998192

Public ClinicalTrials.gov record NCT00998192. 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 18, 2026, 8:27 AM 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 2 Study of Intravenous Administration of REOLYSIN® (Reovirus Type 3 Dearing) in Combination With Paclitaxel and Carboplatin in Patients With Squamous Cell Carcinoma of the Lung

Brief summary

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

The purpose of this Phase 2 study is to investigate whether intravenous administration of REOLYSIN therapeutic reovirus in combination with paclitaxel and carboplatin is effective and safe in the treatment of squamous cell carinoma of the lung.

Study identification

NCT ID
NCT00998192
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Oncolytics Biotech
Industry
Enrollment
32 participants

Conditions and interventions

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
Oct 2009 (Type not available)
Primary completion
Sep 2013 (Actual)
Completion
Aug 2015 (Actual)
Last update posted
Mar 31, 2016

2009 – 2015

United States locations

U.S. sites
17
U.S. states
9
U.S. cities
16
Facility City State ZIP Site status
Cedars-Sinai Medical Center Los Angeles California 90048 —
Ocala Oncology Center Ocala Florida 34471 —
Illinois Cancer Specialists Niles Illinois 60714 —
Investigative Clinical Research of Indiana, LLC Indianapolis Indiana 46260 —
Advanced Oncology Associates Armonk New York 10504 —
Signal Point Clinical Research Center, LLC Middletown Ohio 45042 —
Medical Oncology Associates of Wyoming Valley Kingston Pennsylvania 18704 —
Texas Oncology - Arlington South Arlington Texas 76014 —
Texas Oncology - Bedford Bedford Texas 76022 —
Texas Oncology - Denton South Denton Texas 76210 —
Texas Oncology - Fort Worth Fort Worth Texas 76104 —
Texas Oncology - Garland Garland Texas 75042 —
Texas Oncology - Lewisville Lewisville Texas 75067 —
Cancer Therapy & Research Center at UTHSCSA San Antonio Texas 78229 —
Cancer Care Centers of South Texas San Antonio Texas 78258-3912 —
Texas Oncology - Tyler Tyler Texas 75702 —
Lynchburg Hematology Oncology Clinic Lynchburg Virginia 24501 —

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 NCT00998192, 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 Mar 31, 2016 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00998192 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →