TerminatedPhase 2NCT00372073

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

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

Checked against the public recordLast updated Dec 22, 2021 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 2
U.S. locations20
SponsorCyclacel Pharmaceuticals, Inc.
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 2
Sponsor
Cyclacel Pharmaceuticals, Inc.
Interventions being studied
Drug: seliciclib; Drug: placebo
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

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

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Arizona Cancer CenterTucson, Arizona
  • Pacific Coast Hematology Oncology GroupFountain Valley, California
  • Pasco Hernando OncologyNew Port Richey, Florida
  • Rush University Medical CenterChicago, Illinois
  • The University of ChicagoChicago, Illinois
  • University of Maryland, Greenebaun Cancer CenterBaltimore, Maryland
  • Dana Farber Cancer InstituteBoston, Massachusetts
  • Nebraska Medical CenterOmaha, Nebraska
  • Nevada Cancer Research FoundationLas Vegas, Nevada
  • VA Sierra Nevada Health Care SystemReno, Nevada
  • New Mexico Oncology Hematology ConsultantsAlbuquerque, New Mexico
  • Columbia Presbyterian Medical CenterNew York, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Dec 22, 2021. Always confirm current availability with the study team.

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