Study of GRN163L With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non Small Cell Lung Cancer
Status: | Completed |
---|---|
Conditions: | Lung Cancer, Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | July 2007 |
End Date: | April 2011 |
A Phase I Study of GRN163L in Combination With Paclitaxel and Carboplatin in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer
The purpose of this study is to determine the safety and the maximum tolerated dose (MTD) of
GRN163L when administered in combination with a standard paclitaxel/carboplatin regimen to
patients with advanced or metastatic non-small cell lung cancer.
GRN163L when administered in combination with a standard paclitaxel/carboplatin regimen to
patients with advanced or metastatic non-small cell lung cancer.
GRN163L is a telomerase template antagonist with in vitro and in vivo activity in a variety
of tumor model systems. Telomerase is an enzyme that is active primarily in tumor cells and
is crucial for the indefinite growth of tumor cells. Inhibition of telomerase may result in
antineoplastic effects.
of tumor model systems. Telomerase is an enzyme that is active primarily in tumor cells and
is crucial for the indefinite growth of tumor cells. Inhibition of telomerase may result in
antineoplastic effects.
Inclusion Criteria:
- Histologically or cytologically confirmed diagnosis of NSCLC
- Stage IIIb with pleural effusion, Stage IV, or recurrent disease
- Measurable or evaluable disease by RECIST criteria
- ECOG performance status 0-1
- Adequate hepatic/renal function and platelet count
- If previously treated with an anthracycline, anthracenedione, or trastuzumab, must
have left ventricular ejection fraction > 50%
Exclusion Criteria:
- More than 2 prior chemotherapy regimens for metastatic disease (prior adjuvant
chemotherapy is allowed)
- Tumor progression during treatment with paclitaxel (refractory to paclitaxel)
- Taxane-based regimen within 12 weeks
- Any systemic therapy for cancer within 4 weeks
- Anti-platelet therapy within 2 weeks, other than low dose aspirin prophylaxis therapy
- Therapeutic anticoagulation therapy except for low dose warfarin (eg, 1 mg by mouth
per day)
- Radiation therapy within 3 weeks
- Major surgery within 4 weeks (central line placement is allowed)
- Prolongation of PT or aPTT > the ULN or fibrinogen < the LLN
- History of or active central nervous system metastatic disease
- Any other active malignancy
- Active or chronically recurrent bleeding (eg, active peptic ulcer disease)
- Clinically significant infection
- Active autoimmune disease requiring immunosuppressive therapy
- Clinically significant cardiovascular disease or condition
We found this trial at
4
sites
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22 South Greene Street
Baltimore, Maryland 21201
Baltimore, Maryland 21201
410-328-7904
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University of Maryland Greenebaum Cancer Center The University of Maryland Marlene and Stewart Greenebaum Cancer...
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University of Texas Southwestern Medical Center UT Southwestern is an academic medical center, world-renowned for...
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