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contrast agent p792

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

Description

contrast agent P792: a gadolinium macrocyclic compound based on a Gd-DOTA structure substituted by hydrophilic arms; rapid clearance blood pool agent for magnetic resonance imaging; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID91668170
MeSH IDM0399194

Synonyms (4)

Synonym
hydrogen (2,2',2',2'''-(1,4,7,10-tetraazacyclododecane-1,4,7,10-triyl)tetrakis(5-((2-((4-((4-((2-((3,5-bis(bis((2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl-2,4,6-tribromo)carbamoyl)phenyl)amino)-2-oxoethyl)carbamoyl)phenyl)carbamoyl)phenyl)amino)-2-oxoethyl)
p792 ,
unii-lf24366z4o
contrast agent p792

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The safety controls consisted of complete pre- and postdose physical examinations, measurement of vital signs, clinical laboratory investigations, and monitoring of adverse events (up to 22 days after injection)."( Safety and pharmacokinetics of p792, a new blood-pool agent: results of clinical testing in nonpatient volunteers.
Bonnemain, B; Chassard, D; Gaillard, S; Kubiak, C; Stolz, C, 2002
)
0.31
"No serious adverse events occurred during the study."( Safety and pharmacokinetics of p792, a new blood-pool agent: results of clinical testing in nonpatient volunteers.
Bonnemain, B; Chassard, D; Gaillard, S; Kubiak, C; Stolz, C, 2002
)
0.31
"P792 appeared to be a safe and well-tolerated RCBPA in nonpatient subjects."( Safety and pharmacokinetics of p792, a new blood-pool agent: results of clinical testing in nonpatient volunteers.
Bonnemain, B; Chassard, D; Gaillard, S; Kubiak, C; Stolz, C, 2002
)
0.31

Pharmacokinetics

ExcerptReferenceRelevance
" As a result of this high molecular volume, P792 presents an unusual pharmacokinetic profile, as it is a Rapid Clearance Blood Pool Agent (RCBPA) characterized by limited diffusion across the normal endothelium."( P792: a rapid clearance blood pool agent for magnetic resonance imaging: preliminary results.
Corot, C; Dencausse, A; Devoldere, L; Idée, JM; Le Greneur, S; Meyer, D; Port, M; Raynal, I; Rousseaux, O; Simonot, C, 2001
)
0.31
"To summarize the physicochemical characterization, pharmacokinetic behavior, and biological evaluation of P792, a new monogadolinated MRI blood-pool agent."( Physicochemical and biological evaluation of P792, a rapid-clearance blood-pool agent for magnetic resonance imaging.
Bonnemain, B; Corot, C; Dencausse, A; Idee, JM; Lancelot, E; Lautrou, J; Meyer, D; Port, M; Raynal, I, 2001
)
0.31
" The pharmacokinetic and biodistribution profiles were studied in rabbits."( Physicochemical and biological evaluation of P792, a rapid-clearance blood-pool agent for magnetic resonance imaging.
Bonnemain, B; Corot, C; Dencausse, A; Idee, JM; Lancelot, E; Lautrou, J; Meyer, D; Port, M; Raynal, I, 2001
)
0.31
" The pharmacokinetic and biodistribution profiles are consistent with that of a rapid-clearance blood-pool agent: P792 is mainly excreted by glomerular filtration, and its diffusion across normal endothelium is limited."( Physicochemical and biological evaluation of P792, a rapid-clearance blood-pool agent for magnetic resonance imaging.
Bonnemain, B; Corot, C; Dencausse, A; Idee, JM; Lancelot, E; Lautrou, J; Meyer, D; Port, M; Raynal, I, 2001
)
0.31
" The pharmacokinetic and biodistribution profiles are consistent with those of a rapid-clearance blood-pool agent."( Physicochemical and biological evaluation of P792, a rapid-clearance blood-pool agent for magnetic resonance imaging.
Bonnemain, B; Corot, C; Dencausse, A; Idee, JM; Lancelot, E; Lautrou, J; Meyer, D; Port, M; Raynal, I, 2001
)
0.31
" For pharmacokinetic analysis, the determination of P792 was performed using the ICP-MS technique for blood and urine samples up to 22 days."( Safety and pharmacokinetics of p792, a new blood-pool agent: results of clinical testing in nonpatient volunteers.
Bonnemain, B; Chassard, D; Gaillard, S; Kubiak, C; Stolz, C, 2002
)
0.31
"Due to its physicochemical and pharmacokinetic properties, P792 allows the use of a reduced dosage of gadolinium, resulting in less T2* effect without compromising T1 enhancement."( Renal functional contrast-enhanced magnetic resonance imaging: evaluation of a new rapid-clearance blood pool agent (p792) in sprague-dawley rats.
Claudon, M; Corot, C; Felblinger, J; Grenier, N; Mandry, D; Odille, F; Pedersen, M; Robert, P, 2005
)
0.33
"A physiological pharmacokinetic (PBPK) model was used to estimate tumor microcirculation in nude mice with a grafted tumor."( Evaluation of antiangiogenic treatment effects on tumors' microcirculation by Bayesian physiological pharmacokinetic modeling and magnetic resonance imaging.
Balvay, D; Bessoud, B; Bois, FY; Brochot, C; Cuénod, CA; Siauve, N, 2006
)
0.33

Dosage Studied

ExcerptRelevanceReference
"3) or half dosage (65."( Renal functional contrast-enhanced magnetic resonance imaging: evaluation of a new rapid-clearance blood pool agent (p792) in sprague-dawley rats.
Claudon, M; Corot, C; Felblinger, J; Grenier, N; Mandry, D; Odille, F; Pedersen, M; Robert, P, 2005
)
0.33
"Due to its physicochemical and pharmacokinetic properties, P792 allows the use of a reduced dosage of gadolinium, resulting in less T2* effect without compromising T1 enhancement."( Renal functional contrast-enhanced magnetic resonance imaging: evaluation of a new rapid-clearance blood pool agent (p792) in sprague-dawley rats.
Claudon, M; Corot, C; Felblinger, J; Grenier, N; Mandry, D; Odille, F; Pedersen, M; Robert, P, 2005
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (35)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's27 (77.14)29.6817
2010's5 (14.29)24.3611
2020's3 (8.57)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.83

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index10.83 (24.57)
Research Supply Index3.71 (2.92)
Research Growth Index4.54 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.83)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials3 (8.11%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other34 (91.89%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]