CompletedPhase 1NCT00104767

Celecoxib in Treating Patients With Stage IIIB or Stage IV Non-Small Cell Lung Cancer

RATIONALE: Celecoxib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It may also stimulate the immune system in different ways and stop tumor cells from growing. PURPOSE: This phase I trial is studying the side effects and best dose of celecoxib in treating patients with stage IIIB or stage IV non-small cell lung cancer.

Checked against the public recordLast updated Oct 2, 2015 · Source: ClinicalTrials.gov

StatusCompleted
PhasePhase 1
U.S. locations1
SponsorJonsson Comprehensive Cancer Center
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1
Sponsor
Jonsson Comprehensive Cancer Center
Interventions being studied
Drug: celecoxib
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: * Histologically confirmed non-small cell lung cancer * Stage IIIB or IV disease * Radiographically measurable disease * 18 and over * Performance status: ECOG 0-2 * Renal: Creatinine ≤ 2 mg/dL * Negative pregnancy test * Fertile patients must use effective contraception * More than 4 weeks since prior chemotherapy * Endocrine therapy: More than 4 weeks since prior corticosteroids; No concurrent corticosteroids, including chronic corticosteroids, except for medically-indicated topical steroids * Radiotherapy: More than 4 weeks since prior radiotherapy * More than 4 weeks since other prior anticancer therapy * More than 4 weeks since prior non-cytotoxic investigational agents * At least 72 hours since prior nonsteroidal anti-inflammatory drugs (NSAIDs) Exclusion Criteria: * pregnant or nursing * comorbid disease, psychiatric condition, chronic medical condition, or laboratory abnormality that would preclude study treatment or compliance with study requirements * hypersensitivity to celecoxib, sulfonamides, aspirin, other NSAIDs, or any study reagent * history of gastrointestinal ulceration, bleeding, or perforation * other concurrent cyclooxygenase-2 or -3 inhibitors * other concurrent NSAIDs

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

  • Jonsson Comprehensive Cancer Center at UCLALos Angeles, California

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 2, 2015. Always confirm current availability with the study team.

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