TerminatedPhase 1 / Phase 2NCT00153842

A Study of Paclitaxel and Carboplatin in Combination With Bexarotene Oral Capsules in Patients With Advanced Lung Cancer

The primary aim is to evaluate the safety (Phase I components) of administering bexarotene (Targretin®, LGD1069) oral capsules in combination with two Taxol® and carboplatin (Paraplatin®) schedules to patients with stage IIIB and IV non-small cell lung cancer. This study will also evaluate the preliminary efficacy (Phase II component) of bexarotene oral capsules in combination with the weekly Taxol® schedule and carboplatin in these patients.

Checked against the public recordLast updated Mar 6, 2019 · Source: ClinicalTrials.gov

StatusTerminated
PhasePhase 1 / Phase 2
U.S. locations1
SponsorDartmouth-Hitchcock Medical Center
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1 / Phase 2
Sponsor
Dartmouth-Hitchcock Medical Center
Interventions being studied
Drug: Bexarotene (targretin); Drug: Bexarotene (targretin)
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: * unresectable stage IIIB or IV NSCLC * adequate bone marrow, hepatic, thyroid and renal function Exclusion Criteria: * peripheral neuropathy \>= grade 2 * gastrointestinal abnormalities * known hypersensitivity to retinoids

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

  • Norris Cotton Cancer CenterLebanon, New Hampshire

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Mar 6, 2019. Always confirm current availability with the study team.

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