Page last updated: 2024-12-08

esorubicin

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

esorubicin: RN given refers to parent cpd; synthesized deriv of doxorubicin [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12959501
MeSH IDM0097338

Synonyms (1)

Synonym
esorubicin

Research Excerpts

Pharmacokinetics

ExcerptReferenceRelevance
" Pharmacokinetic analysis revealed large interpatient variation in plasma drug levels."( Pharmacokinetic and phase I evaluation of esorubicin (4'-deoxydoxorubicin) by continuous infusion over forty-eight hours in patients with leukemia.
Allen, SL; Budman, DR; Chan, K; Kreis, W; Rottach, C; Schulman, P; Vinciguerra, V; Weiselberg, L, 1988
)
0.27
" Each molecule is characterized by original metabolic and pharmacokinetic features, which can be compared to those of the reference anthracyclines, doxorubicin and daunorubicin."( [Pharmacokinetics of new anthracyclines].
Robert, J, 1988
)
0.27
" Esorubicin disappeared from plasma according to a tri-exponential pattern with a terminal half-life of 20."( Human pharmacokinetics of esorubicin (4'-deoxydoxorubicin).
Bachur, NR; Crespeigne, N; Davis, TA; Dodion, P; Kenis, Y; Rozencweig, M, 1985
)
0.27
"The pharmacokinetic of 4'-deoxydoxorubicin, a new analog of doxorubicin, was compared with that of its parent compound in mice treated with equal and equiactive doses."( Fluorescence assays and pharmacokinetic studies of 4'-deoxydoxorubicin and doxorubicin in organs of mice bearing solid tumors.
Casazza, AM; di Marco, A; Formelli, F; Mariani, A; Pollini, C, 1981
)
0.26

Dosage Studied

Esorubicin is given in a dosage of 30 mg/m2 intravenously every 3 weeks. Phase II trials are clearly warranted in a wide variety of metastatic neoplasms.

ExcerptRelevanceReference
" The starting esorubicin dosing schedule was 30 mg/m2 every 3 weeks for good risk patients and 25 mg/m2 every 3 weeks for poor risk patients."( A phase II evaluation of esorubicin in ovarian cancer. A Southwest Oncology Group study.
Abbott, TM; Alberts, DS; Mason-Liddil, N; O'Toole, RV; Salmon, SE; Stock-Novack, D, 1992
)
0.28
" DXDX has minimal activity against non-small cell lung cancer as a single agent at the dosage used in this study."( Phase II trial of 4' deoxydoxorubicin (DXDX) for unresectable non-small cell bronchogenic carcinoma. An Illinois Cancer Council study.
Blough, RR; Johnson, CM; Kilton, LJ; Lad, TE; Rose, C; Rosen, ST; Rossof, AH; Schor, J, 1990
)
0.28
"Forty-six eligible women with advanced metastatic breast cancer were entered on a Phase II trial utilizing esorubicin (4'-deoxydoxorubicin) given in a dosage of 30 mg/m2 intravenously every 3 weeks."( Esorubicin (4'-deoxydoxorubicin, NSC 267469) in advanced breast cancer. A phase II study of the CALGB.
Campbell, T; Henderson, IC; Korzun, AH; Muss, HB; Rice, MA; Van Echo, D; Vogelzang, NJ; Wood, W, 1990
)
0.28
"4'-Deoxydoxorubicin was given to 15 patients with drug-resistant pediatric malignant solid tumors with the objectives of determining the maximum tolerated dosage and dose-limiting toxicity."( Phase I study of 4'-deoxydoxorubicin (esorubicin) in children with malignant solid tumors.
Avery, L; Douglass, EC; Hayes, FA; Horowitz, ME; Meyer, WH; Pratt, CB; Thompson, EI, 1989
)
0.28
" Dosage levels extended from 35 to 85 mg/m2."( Pharmacokinetic and phase I evaluation of esorubicin (4'-deoxydoxorubicin) by continuous infusion over forty-eight hours in patients with leukemia.
Allen, SL; Budman, DR; Chan, K; Kreis, W; Rottach, C; Schulman, P; Vinciguerra, V; Weiselberg, L, 1988
)
0.27
" Phase II trials with esorubicin in this dosage schedule are clearly warranted in a wide variety of metastatic neoplasms including a substantial population of patients who have not received prior chemotherapy."( Phase I trial of esorubicin (4'deoxydoxorubicin).
Alberts, DS; Brooks, R; Garewal, HS; Jones, SE; Robertone, A; Salmon, SE, 1984
)
0.27
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (100)

TimeframeStudies, This Drug (%)All Drugs %
pre-199079 (79.00)18.7374
1990's21 (21.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials20 (17.39%)5.53%
Reviews8 (6.96%)6.00%
Case Studies3 (2.61%)4.05%
Observational0 (0.00%)0.25%
Other84 (73.04%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (3)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Phase II, Open Label, Non-Randomized, Efficacy and Safety Study of an Intravenous Formulation of the Anthracycline Analog, GPX-100, in the Treatment of Metastatic Breast Cancer [NCT00123877]Phase 240 participants Interventional2005-03-31Terminated
Phase I Trial of 4'-IODO-4'-Deoxydoxorubicin in Primary Amyloidosis (AL) [NCT00030381]Phase 122 participants (Actual)Interventional2001-12-31Terminated(stopped due to Administratively complete.)
Phase II Trial of 4'-IODO-4'-Deoxydoxorubicin in Primary Amyloidosis (AL) [NCT00003853]Phase 245 participants (Anticipated)Interventional1999-04-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]