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OpenTrials
Completed

NCT Number: NCT00569114

Phase 1 Study of TG01 and Erlotinib in Non-small Cell Lung Cancer (NCSLC) Patients

This is a multicenter, open-label, phase 1, dose escalation study. The purpose is to determine the highest dose of TG01 that can be safely given to patients with Non-Small Cell Lung Cancer in combination with erlotinib.

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Key information

Conditions

Non-small Cell Lung Cancer Bronchial Neoplasms Carcinoma, Bronchogenic Carcinoma, Non-Small-Cell Lung Lung Diseases Lung Neoplasms Neoplasms Neoplasms by Site Respiratory Tract Diseases Respiratory Tract Neoplasms Thoracic Neoplasms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Comprehensive Blood and Cancer Center, Bakersfield, California, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(include but are not limited to):

  • Histogically or pathologically determined relapsed/recurrent Stage IIIb (plueral effusion) or IV NSCLC.
  • Measurable or evaluable disease as defined by RECIST
  • Must have failed at least one prior chemotherapy regimen or have refused chemotherapy.
  • ECOG perfromance status of 0,1, or 2.

Exclusion criteria

(include but are not limited to):

  • Radiation therapy (excluding CNS therapy) < 2 weeks, chemotherapy, non-cytotoxic investigational agents or high dose corticosteroids within 3 weeks of intitating therpy or patients who have not recovered from adverse effects due to agents administered more than 3 weeks earlier.
  • Evidence of New York Heart Associatation Class III or greater cardiac disease.
  • History of myocardial infarction, stroke, or cardiovascular intervention within the last 12 months.
  • Patients on anti-platlet drugs or anticoagulants such as Placix and Coumadin.
  • Systemic central nervous system metastases. The patient must be stable after radiotherapy for >/= to 2 weeks and off corticosteroids for >/= to 1 week.
  • Pregnant or nursing women.
  • Patients who are primarily refactory to erlotinib.

Treatment and study plan

TG01

Drug

Drug:TG01tablets given orally QD Drug: erlotinib tablets 150mg QD

Primary outcomes

  1. Saftey, maximum tolerated dose, optimal biological dose and pharmacokinetics.

    Time frame: Baseline, 8, 15 and 28 days

Interested in participating?

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Sponsors and collaborators

Lead sponsor

Tragara Pharmaceuticals, Inc.

Industry

Registry information

Official study title

A Phase 1 Dose-Escalation Pharmacokinetic and Pharmacodynamic Study of TG01 Tablets in Combination With Erlotinib in Non-Small Cell Lung Cancer Patients

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Dec 6, 2007
Registry last updated
Mar 17, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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