Phase I and pharmacokinetic study of erlotinib for solid tumors in patients with hepatic or renal dysfunction: CALGB 60101.
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Citation:
J Clin Oncol vol 25 (21) 3055-60
Year:
2007
Type:
Manuscript
Funding:
NCTN
Endpoint:
Primary
Analysis:
Primary
Data Sharing:
No-Data-Sharing
Status:
Presented/Published
Citation Status:
pub
Note:
Methodological:
No
Biospecimen:
No
SDC:
No
Book Volume:
Parents:
None
Children:
None
Program:
OGC
Primary Committee:
Experimental
Sec. Committees:
   
Pharmas:
 
Grants:
CA 02599, CA 03927, CA 04326, CA 11028, CA 31946, CA 31983, CA 33601, CA 35279, CA 37135, CA 41287, CA 47577, CA 47642, CA 77597, CA 77658  
Corr. Author:
 
Authors:
                         
Networks:
 
Study
CALGB-60101
Multiple Studies, or Legacy Studies in Alliance Study:
Phases:
1
Keywords:
Administration, Oral, Adult, Aged, Dose-Response Relationship, Drug, Drug Administration Schedule, Erlotinib Hydrochloride, Female, Follow-Up Studies, Humans, Kidney Diseases, Kidney Function Tests, Liver Diseases, Liver Function Tests, Male, Maximum Tolerated Dose, Middle Aged, Neoplasm Staging, Neoplasms, Probability, Quinazolines, Risk Assessment, Survival Analysis, Treatment Outcome