US2007231266A1PendingUtilityA1

Diagnosis of macrophage mediated disease

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Assignee: LOW PHILIP SPriority: May 2, 2001Filed: Dec 29, 2006Published: Oct 4, 2007
Est. expiryMay 2, 2021(expired)· nominal 20-yr term from priority
A61P 37/06A61P 9/10A61P 37/02A61P 37/00A61P 31/04A61P 25/00A61P 29/00A61P 19/04A61K 47/6849A61K 51/0482A61K 9/127A61P 1/00A61P 19/00A61K 47/646A61P 11/00A61P 19/02A61P 17/00A61P 1/04A61K 51/1027A61K 49/00
59
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Claims

Abstract

The invention relates to a method of treating or monitoring/diagnosing a disease state mediated by activated macrophages. The method comprises the step of administering to a patient suffering from a macrophage mediated disease state an effective amount of a composition comprising a conjugate or complex of the general formula A b -X where the group A b comprises a ligand capable of binding to activated macrophages, and when the conjugate is being used for treatment of the disease state, the group X comprises an immunogen, a cytotoxin, or a compound capable of altering macrophage function, and when the conjugate is being used for monitoring/diagnosing the disease state, X comprises an imaging agent. The method is useful for treating a patient suffering from a disease selected from the group consisting of rheumatoid arthritis, ulcerative colitis, Crohn's disease, inflammation, infections, osteomyelitis, atherosclerosis, organ transplant rejection, pulmonary fibrosis, sarcoidosis, and systemic sclerosis.

Claims

exact text as granted — not AI-modified
1 - 19 . (canceled)  
     
     
         20 . A method of monitoring/diagnosing a disease state mediated by activated macrophages, said method comprising the step of administering to a patient suffering from the macrophage mediated disease state an effective amount of a composition comprising a conjugate or complex of the general formula  
         A b -X  
       wherein the group A b  comprises a folate receptor binding ligand capable of binding to the activated macrophages and the group X comprises an imaging agent.  
     
     
         21 . The method of  claim 20  wherein the group X further comprises a liposome.  
     
     
         22 . The method of  claim 20  wherein the imaging agent comprises a metal chelating moiety.  
     
     
         23 . The method of  claim 22  wherein the imaging agent further comprises a metal cation.  
     
     
         24 . The method of  claim 23  wherein the metal cation is a radionuclide.  
     
     
         25 . The method of  claim 23  wherein the metal cation is a nuclear magnetic resonance imaging enhancing agent.  
     
     
         26 . The method of  claim 20  wherein the patient is suffering from a disease state selected from the group consisting of rheumatoid arthritis, ulcerative colitis, Crohn's disease, inflammatory lesions, infections of the skin, osteomyelitis, atherosclerosis, organ transplant rejection, pulmonary fibrosis, sarcoidosis, systemic sclerosis, and any chronic inflammation.  
     
     
         27 . The method of  claim 20  further comprising the step of performing an imaging procedure about 1 hour to about 6 hours post-administration of the conjugate.

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