Claims for Patent: 9,879,325
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Summary for Patent: 9,879,325
Title: | Method for predicting the responsiveness a patient to a treatment with an anti-CD20 antibody |
Abstract: | The present invention relates to a method for predicting the responsiveness of a patient to a treatment with an anti-CD20 antibody, said method comprising measuring the level of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) expression in B cells obtained from said patient. |
Inventor(s): | Chiche; Johanna (Nice, FR), Thieblemont; Catherine (Paris, FR), Ricci; Jean-Ehrland (Nice, FR) |
Assignee: | ASSISTANCE PUBLIQUE--HOPITAUX DE PARIS (Paris, FR) UNIVERSITE PARIS DIDEROT (PARIS VII) (Paris, FR) UNIVERSITE DE NICE--SOPHIA ANTIPOLIS (Nice, FR) INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (Paris, FR) |
Application Number: | 15/121,864 |
Patent Claims: | 1. A method for treating a patient having non Hodgkin's B cell lymphoma wherein the non Hodgkin's B cell lymphoma is diffuse large B-cell lymphoma, said method
comprising the steps of: a) identifying a responder patient having diffuse large B-cell lymphoma that is responsive to treatment with an anti human CD20 antibody by measuring a level of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) expression in tumor
B-cells obtained from said patient, wherein a high level of GAPDH expression is predictive of a response to said anti-CD20 antibody treatment; and b) treating with said anti-CD20 antibody the responder patient identified.
2. The method according to claim 1, wherein the anti-CD20 antibody is selected from the group consisting of rituximab, ibritumomab, ofatumumab, ocrelizumab, PRO131921,veltuzumab, AME-133v, tositumomab, and GA-101. 3. The method according to claim 1, wherein the anti-CD20 antibody is rituximab. |
Details for Patent 9,879,325
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Genentech, Inc. | RITUXAN | rituximab | Injection | 103705 | 11/26/1997 | ⤷ Try a Trial | 2034-03-03 |
Novartis Pharmaceuticals Corporation | ARZERRA | ofatumumab | Injection | 125326 | 10/26/2009 | ⤷ Try a Trial | 2034-03-03 |
Novartis Pharmaceuticals Corporation | ARZERRA | ofatumumab | Injection | 125326 | 04/01/2011 | ⤷ Try a Trial | 2034-03-03 |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |
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