US2015119331A1PendingUtilityA1
Use of Histones for Therapeutic Purposes
Assignee: SYMBIOTEC GENELLSCHAFT ZUR ERFORSHUNG AUF DEM GEIBEIT DER BIOTECHNOLOGIE MBHPriority: May 10, 2005Filed: Jan 2, 2015Published: Apr 30, 2015
Est. expiryMay 10, 2025(expired)· nominal 20-yr term from priority
A61P 7/00A61P 7/02A61P 35/02A61P 7/04A61K 38/1709A61K 38/00A61K 38/16
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Claims
Abstract
The invention relates to the use of at least one human recombinant histone, especially at least one histone H1 subtype, and/or a therapeutic histone fraction as a basis for the treatment of thrombocytopenia.
Claims
exact text as granted — not AI-modified1 - 7 . (canceled)
8 . A method for treating thrombocytopenia in a patient in need thereof, the method comprising: administering to the patient at least three doses of a pharmaceutical composition comprising histone H1.3 or a therapeutically active histone H1.3 segment during a period of at least 8 days, wherein administration of the pharmaceutical composition increases the number of platelets in the peripheral blood, thereby treating the thrombocytopenia.
9 . The method according to claim 8 , wherein the thrombocytopenia results from a hematological disorder.
10 . The method according to claim 9 , wherein the hematological disorder is a leukemia.
11 . The method according to claim 10 , wherein the leukemia is an acute myeloid leukemia.
12 . The method according to claim 8 , wherein the treatment of the thrombocytopenia occurs concurrently with or after a therapy for a hematological disorder.
13 . The method according to claim 12 , wherein the therapy is a chemotherapy.
14 . The method according to claim 12 , wherein the hematological disorder is a leukemia.
15 . The method according to claim 14 , wherein the leukemia is an acute myeloid leukemia.
16 . The method according to claim 8 , wherein the administration is intravenous.
17 . The method according to claim 8 , further comprising the administration of other human recombinant subtypes of histone H1 in combination with the histone H1.3 or therapeutically active histone H1.3 segment.
18 . A method for treating thrombocytopenia in a patient in need thereof caused by a primary disorder, comprising: administering to the patient a pharmaceutical composition comprising histone H1.3 or a therapeutically active histone H1.3 segment, wherein the histone H1.3 is not effective to treat the primary disorder.
19 . The method according to claim 18 , wherein the thrombocytopenia results from a hematological disorder.
20 . The method according to claim 18 , wherein the treatment of the thrombocytopenia occurs concurrently with or after a therapy for a hematological disorder.
21 . The method according to claim 20 , wherein the therapy is a chemotherapy.
22 . The method according to claim 18 , wherein administration to the patient is administration of at least three doses of a pharmaceutical composition comprising histone H 1 . 3 or a therapeutically active histone H 1 . 3 segment during a period of at least 8 days.
23 . The method according to claim 18 , wherein the administration is intravenous.
24 . The method according to claim 18 , further comprising the administration of other human recombinant subtypes of histone H1 in combination with the histone H1.3 or therapeutically active histone H1.3 segment.
25 . A method for treating threatening or incipient thrombocytopenia in a patient which is expected to be caused by chemotherapy, comprising: administering to the patient a pharmaceutical composition comprising histone H1.3 or a therapeutically active histone H1.3 segment concurrently with chemotherapy.
26 . The method according to claim 25 , wherein the administration is intravenous.
27 . The method according to claim 25 , further comprising the administration of other human recombinant subtypes of histone H1 in combination with the histone H1.3 or therapeutically active histone H1.3 segment.Join the waitlist — get patent alerts
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