Lung Cancer Clinical Trial

Efficacy Study of Oral Seliciclib to Treat Non-Small Cell Lung Cancer

Summary

A phase 2 study to evaluate efficacy of oral seliciclib in treating non-small cell lung cancer (NSCLC).

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Full Description

A randomized Phase II study of an experimental anti-cancer drug called seliciclib with objectives of evaluating safety and efficacy in patients with non-small cell lung cancer.

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Eligibility Criteria

Inclusion Criteria:

Adult patients with histologically-confirmed recurrent non-small cell lung cancer have had at least two prior systemic treatment regimens
Must have measurable disease according to RECIST
Eastern Cooperative Oncology Group performance status 0-1
Adequate bone marrow, hepatic and renal function
Ability to swallow capsules
At least 3 weeks from prior systemic treatments including investigational anti-cancer therapy, at least 7 days from prior radiation therapy and have recovered from prior toxicities
At least 3 weeks from major surgery

Exclusion Criteria:

Non-small cell cancer histology contains a component of small cell lung cancer
Previously untreated CNS metastasis or progressive CNS metastasis
Prior treatment with a CDK inhibitor
Currently receiving radiotherapy, biological therapy, or any other investigational therapy
Uncontrolled intercurrent illness
Having other cancers that have been treated with chemotherapy or biological therapy in the past 5 years with the exception of adequately treated in situ cervical cancer or basal cell skin cancer
Pregnant or lactating women
Known to be HIV-positive
Active hepatitis B and/or hepatitis C infection

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

187

Study ID:

NCT00372073

Recruitment Status:

Terminated

Sponsor:

Cyclacel Pharmaceuticals, Inc.

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There are 20 Locations for this study

See Locations Near You

Arizona Cancer Center
Tucson Arizona, 85724, United States
Pacific Coast Hematology Oncology Group
Fountain Valley California, 92708, United States
Pasco Hernando Oncology
New Port Richey Florida, 34652, United States
Rush University Medical Center
Chicago Illinois, 60612, United States
The University of Chicago
Chicago Illinois, 60637, United States
University of Maryland, Greenebaun Cancer Center
Baltimore Maryland, 21201, United States
Dana Farber Cancer Institute
Boston Massachusetts, 02115, United States
Nebraska Medical Center
Omaha Nebraska, 68198, United States
Nevada Cancer Research Foundation
Las Vegas Nevada, 89106, United States
VA Sierra Nevada Health Care System
Reno Nevada, 89502, United States
New Mexico Oncology Hematology Consultants
Albuquerque New Mexico, 87109, United States
Columbia Presbyterian Medical Center
New York New York, 10032, United States
Penn State Milton S. Hershey Medical Center
Hershey Pennsylvania, 17033, United States
University of Pittsburg Cancer Institute
Pittsburgh Pennsylvania, 15232, United States
The Family Cancer Center
Collierville Tennessee, 38017, United States
Vanderbilt University Medical Center
Nashville Tennessee, 37232, United States
Southwest Regional Cancer Center
Austin Texas, 78705, United States
Center for Oncology Research and Treatment
Dallas Texas, 75230, United States
East Texas Medical Center
Tyler Texas, 75701, United States
Danville Hematology Oncology
Danville Virginia, 24541, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

187

Study ID:

NCT00372073

Recruitment Status:

Terminated

Sponsor:


Cyclacel Pharmaceuticals, Inc.

How clear is this clinincal trial information?

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