US2016292389A1PendingUtilityA1

Method for distribution of a drug

Assignee: BIOGEN MA INCPriority: Aug 9, 2006Filed: Jun 13, 2016Published: Oct 6, 2016
Est. expiryAug 9, 2026(~0.1 yrs left)· nominal 20-yr term from priority
G06Q 10/083G06F 19/363G06F 19/3468G16H 70/40G16H 20/00G16H 10/60G06Q 50/22G16H 20/10G16H 10/20Y02A90/10
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Claims

Abstract

A method of providing an anti-VLA-4 antibody to a patient.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of providing an anti-VLA-4 antibody to a patient having relapsing MS comprising:
 (1) collecting patient and prescriber information;   (2) reviewing said information or enrollment form, entering information into a record system, and generating an authorization;   (3) communicating the authorization generated in (2) to a treatment site; and   (4) conducting a treatment site review of a patient including
 i. determining if the treatment site has a current authorization for treatment of the patient; 
 ii. confirming that the treatment site does not have notice that the patient is no longer authorized 
 iii. providing the patient with information about the drug; 
 iv. asking the patient if symptoms have worsened; 
 v. asking the patient if he/she has a contraindicated medical condition; and 
 vi. asking the patient if he/she has taken a contraindicated medication; 
   
       wherein an answer of no to iv, v, and vi allows administration of the drug to the patient and an answer of yes to one of iv, v, or vi requires prescriber override to administer the drug. 
     
     
         2 . The method of  claim 1 , further comprising:
 (5) upon expiration of an authorization, obtaining reauthorization for subsequent treatment prior to subsequent treatment, wherein reauthorization requires certification by the prescriber that
 (a) the patient still under his/her care; 
 (b) the patient is alive; 
 (c) the patient has had no unwanted side effect of the drug, no contraindicated condition, or no contraindicated treatment that the prescriber has not already reported to the central administrator, 
   provided that if the prescriber reauthorizes the patient must still undergo the review in step (4) prior to receiving the drug.   
     
     
         3 . The method of  claim 1 , wherein prior to each shipment of the drug, a distributor of the drug obtains a shipment authorization from the central administrator. 
     
     
         4 . The method of  claim 1 , wherein said drug is shipped only to and administered only at authorized treatment sites. 
     
     
         5 . The method of  claim 1 , wherein central pharmacies that dispense the drug to authorized treatment sites are enrolled in a tracking system. 
     
     
         6 . The method of  claim 1 , wherein the central administrator systematically follows and actively solicits information on every patient that receives the drug regarding any adverse events. 
     
     
         7 . The method of  claim 1 , further comprising administering said anti-VLA4 antibody. 
     
     
         8 . The method of  claim 1 , wherein said anti-VLA4 antibody is natalizumab. 
     
     
         9 . The method of  claim 1 , wherein the method is applied to at least 500 patients. 
     
     
         10 . A system configured to allow the practice of the method of  claim 1  comprising:
 instructions for carrying out the method of  claim 1 ; 
 a user interface for inputting a query; and 
 a processor for generating a query result. 
 
     
     
         11 . The system of  claim 10 , wherein the method carried out by the system further comprises the following step:
 (5) upon expiration of an authorization obtaining reauthorization for subsequent treatment prior to subsequent treatment, wherein reauthorization requires certification by the prescriber that
 (a) the patient still under his/her care; 
 (b) the patient is alive; 
 (c) the patient has had no unwanted side effect of the drug, no contraindicated condition, or no contraindicated treatment that the prescriber has not already reported to the central administrator, 
   provided that if the prescriber reauthorizes the patient must still undergo the review in step (4) prior to receiving the drug.   
     
     
         12 . The system of  claim 10 , wherein the method carried out by the system further requires that prior to each shipment of the drug, a distributor of the drug obtains a shipment authorization from the central administrator. 
     
     
         13 . The system of  claim 10 , wherein the method carried out by the system further requires that said drug is shipped only to and administered only at authorized treatment sites. 
     
     
         14 . The system of  claim 10 , wherein the method carried out by the system further requires that central pharmacies that dispense the drug to authorized treatment sites are enrolled in a tracking system. 
     
     
         15 . The system of  claim 10 , wherein the method carried out by the system further requires that the central administrator systematically follows and actively solicits information on every patient that receives the drug regarding any adverse events. 
     
     
         16 . The system of  claim 10 , wherein said anti-VLA4 antibody is natalizumab. 
     
     
         17 . The system of  claim 10 , wherein said method is applied to at least 500 patients. 
     
     
         18 . A computer program product tangibly embodied in an information carrier and comprising instructions that when executed by a processor provide for performance of the method of  claim 1 . 
     
     
         19 . A database which includes a record all of the forms and information referred to in the method of  claim 1  for a patient. 
     
     
         20 . The database of  claim 19 , having records for at least 100 patients.

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