Inventor
Fulvio Uggeri
Inventor
Codogno, IT
Overview
Patents· 57 as inventor
Public. Assignee & technology derived from the patent record. Each patent links to its LexDana page.
A61Kprimary
A61KPreparations for medical, dental or toiletry purposes26%
C07CAcyclic or carbocyclic compounds22%
C07DHeterocyclic compounds17%
A61PSpecific therapeutic activity of chemical compounds or medicinal preparations10%
C07FAcyclic, carbocyclic or heterocyclic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur, selenium or tellurium3%
C07KPeptides3%
Y10STechnical subjects covered by former uspc cross-reference art collections [xracs] and digests3%
Y10TTechnical subjects covered by former us classification3%
A61BDiagnosis2%
G01RMeasuring electric variables2%
PatentTitleYear
10,682,427Intra-operative imaging202010,328,162CEST systems exhibiting a concentration independent responsiveness201910,232,060CEST systems exhibiting a concentration independent responsiveness20199,795,695'Process for the preparation of gadobenate dimeglumine complex in a solid form'20179,694,090'Process for preparing hyperpolarized substrates and method for MRI'20179,480,758'Diagnostic agents selective against metalloproteases'20169,409,951'Integrin targeted synthetic ligands for diagnostic and therapeutic applications'20169,333,272'Fibrin binding peptide conjugates for diagnostic and therapeutic applications'20169,238,615'Process for the iodination of aromatic compounds'20169,193,659'Process for the iodination of aromatic compounds'20159,012,483'Use of L-Histidine and derivatives thereof'20158,961,933'Process for the preparation of aqueous solutions of hyperpolarized molecules'20158,766,003'Process for the iodination of phenolic derivatives'20148,636,977'Integrin targeted synthetic ligands for diagnostic and therapeutic applications'20148,611,981'MRI-CEST diagnostic technique based on non-punctual analysis'20138,540,966'Contrast agents endowed with high relaxivity'20138,518,373'Ionic and non-ionic radiographic contrast agents for use in combined X-ray and nuclear magnetic resonance diagnostics'20138,329,635'Method for the preparation of specific antibodies against saccharidic antigens'20127,988,950'Contrast agents endowed with high relaxivity for use in magnetic resonance imaging (MRI) which contain a chelating moiety with polyhydroxylated substituents'20116,652,834'Amphipatic polycarboxylic chelates and complexes with paramagnetic metals as MRI contrast agents'2003RE038329'Chelated complexes of paramagnetic metals with low toxicity'20036,461,588'Use of bile acid conjugates, derivatives thereof with metal complexes as blood pool agents for nuclear magnetic resonance diagnostics'20026,342,598'Amphipatic polycarboxylic chelates and complexes with paramagnetic metals as MRI contrast agents'20026,337,064'Manganese chelates with high relaxivity in serum'20026,177,562'Chelated complexes of paramagnetic metals with low toxicity'20016,149,890'Chelated complexes of paramagnetic metals with low toxicity'20006,099,824'Benzyloxy derivatives of DTPA for MRI'20005,763,663'Process for the manufacturing of iodinated contrast agents'19985,728,877'Process for the manufacturing of iodinated contrast agents'19985,708,166'Macrocyclic chelants, their chelates and uses thereof in the diagnostic field'19985,663,413'Biphenyl iodinated derivatives and their diagnostic use'19975,660,814'Iodinated paramagnetic chelates, and their use as contrast agents'19975,649,537'Paramagnetic metal icon chelates and use thereof as contrast agents in magnetic resonance imaging'19975,622,688'Macrocyclic chelants, their chelates and uses thereof in the diagnostic field'19975,587,487'Tetraiodopyrrole derivatives as contrast medium and as antiseptic'19965,539,105'Intermediates for chelating agents with prefixed symmetry and process for their preparation'19965,464,607'5,5\'-/(1,3-propanediyl) bis-/imino(2-oxo-2,1-ethanediyl)acetylimino/bis(2,4,6-triiodo-1,3-benzen edicarboxylamides), and contrast media containing them'19955,424,423'Intermediates for chelating agents with prefixed symmetry and process for their preparation'19955,182,370'Paramagnetic chelates'19935,132,409'Macrocyclic chelating agents and chelates thereof'19925,066,823'Preparation of 5-acylamino-2,4,6-triiodo- or tribromo-benzoic acid derivatives'19914,980,502'Paramagnetic chelates'19904,916,246'Paramagnetic chelates useful for NMR imaging'19904,888,433'Process for the preparation of optically active alpha-arylalkanoic acids and novel intermediates thereof'19894,855,464'Optically active ketals, processes for their preparation and their use in the synthesis of alpha-arylalkanoic acids'19894,810,819'Process for the preparation of optically active alpha-acrylalkanoic acids and novel intermediates thereof'19894,748,253'Process for preparing esters of alkanoic acids via rearrangement of alpha-haloketals'19884,734,507'Optically active ketals, processes for their preparation and their use in the synthesis of alpha-arylalkanoic acids'19884,697,036'Process for the preparation of optically active alpha-arylalkanoic acids and novel intermediates thereof'19874,675,418'Process for preparing alkanoic acids or esters thereof by rearrangement of alpha-halo-ketones in protic medium and in the presence of a non-noble metal salt'19874,642,376'Process for the preparation of alpha-hydroxyaryl-alkanoic acids'19874,620,031'Process for preparing alpha-aryl-alkanoic acids'19864,609,766'Process for preparing esters of 2-(6\'-methoxy-2\'-naphtyl)-propionic acid via rearrangement of new ketals of 2-halo-1-(6\'-methoxy-2\'-naphtyl)-propan-1-one and new esters of 2-(5\'-bromo-6\'-methoxy-2\'-naphtyl)propionic acid thus prepared'19864,582,930'Process for the preparation of optically active alpha-arylalkanoic acids'19864,579,968'Process for the preparation of optically active alpha-arylalkanoic acids'19864,560,777'Preparation of esters of 2-(6\'-methoxy-2\'-naphthyl)-propionic acid via rearrangement of ketals of 2-halo-1-(6\'-methoxy-2\'-naphthyl)-propan-1-one'19854,414,405'Process for preparing esters of 2-(6\'methoxy-2\'naphtyl)-propionic acid via rearrangement of new ketals of 2-halo-1-(6\'-methoxy-2\'-naphtyl)-propan-1-one and new esters of 2-(5\'-bromo-6\'-methoxy-2\'-naphtyl)-propionic acid thus prepared'1983Career & activity timeline
Assembled from patent assignee/location history and declaration credentials.
1983–2020Based in Codogno, IT· patent location history
1986–1989Patents assigned to ZAMBON SPA (9)· patent assignee history
1991–2014Based in Milan, IT· patent location history
1995–2002Patents assigned to DIBRA SPA (15)· patent assignee history
2002–2020Patents assigned to BRACCO IMAGING SPA (21)· patent assignee history
2012–2019Patents assigned to UGGERI FULVIO (14)· patent assignee history
2013–2019Patents assigned to AIME SILVIO (8)· patent assignee history
2013Based in Lodi, IT· patent location history
2016Based in Colleretto Giacosa, IT· patent location history
Inventor activity
Assignee and location history derived from the patent record.
Assignees
| Assignee | Patents | Span |
|---|---|---|
| BRACCO IMAGING SPA | 21 | 2002–2020 |
| DIBRA SPA | 15 | 1995–2002 |
| UGGERI FULVIOself | 14 | 2012–2019 |
| ZAMBON SPA | 9 | 1986–1989 |
| AIME SILVIO | 8 | 2013–2019 |
Locations
| Location | Patents | Span |
|---|---|---|
| Codogno, IT | 33 | 1983–2020 |
| Milan, IT | 21 | 1991–2014 |
| Colleretto Giacosa, IT | 2 | 2016 |
| Lodi, IT | 1 | 2013 |