Use of telomerase inhibitors for the treatment of myeloproliferative disorders and myeloproliferative neoplasms

Patent metadata

Field	Value
Publication number	US-9375485-B2
Application number	US-201313841711-A
Country	US
Kind code	B2
Filing date	Mar 15, 2013
Priority date	Dec 7, 2012
Publication date	Jun 28, 2016
Grant date	Jun 28, 2016

Abstract

Provided herein are methods for reducing neoplastic progenitor cell proliferation and alleviating symptoms associated in individuals diagnosed with or thought to have Essential Thrombocythemia (ET). Also provided herein are methods for using telomerase inhibitors for maintaining blood platelet counts at relatively normal ranges in the blood of individuals diagnosed with or suspected of having ET.

First claim

What is claimed is:

1. A method for alleviating at least one symptom associated with myelofibrosis (MF) or myelodysplastic syndrome in an individual in need thereof, the method comprising: administering a clinically effective amount of a telomerase inhibitor to the individual, wherein administration of the telomerase inhibitor alleviates at least one symptom associated with myelofibrosis (MF) or myelodysplastic syndrome.

2. The method of claim 1 , wherein the symptom comprises headache, dizziness or lightheadedness, chest pain, weakness, fainting, vision changes, numbness or tingling of extremities, redness, throbbing or burning pain in extremities (erythromelalgia), enlarged spleen, nosebleeds, bruising, bleeding from mouth or gums, bloody stool, or stroke.

3. The method of claim 1 wherein the at least one symptom is associated with myelofibrosis (MF).

4. The method of claim 1 wherein the myelodysplastic syndrome is selected from the group consisting of refractory anemia, refractory anemia with excess blasts, refractory cytopenia with multilineage dysplasia, refractory cytopenia with unilineage dysplasia, and chronic myelomonocytic leukemia (CMML).

5. The method of claim 4 wherein the myelodysplastic syndrome (MDS) is chronic myelomonocytic leukemia (CMML).

6. A method for reducing neoplastic progenitor cell proliferation in an individual diagnosed with or suspected of having myelofibrosis (MF) or myelodysplastic syndrome, the method comprising: administering a clinically effective amount of a telomerase inhibitor to the individual, wherein administration of the telomerase inhibitor reduces neoplastic progenitor cell proliferation in the individual.

7. The method of claim 6 wherein the individual is diagnosed with or suspected of having myelofibrosis (MF).

8. The method of claim 6 wherein the myelodysplastic syndrome is selected from the group consisting of refractory anemia, refractory anemia with excess blasts, refractory cytopenia with multilineage dysplasia, refractory cytopenia with unilineage dysplasia, and chronic myelomonocytic leukemia (CMML).

9. The method of claim 6 , wherein the individual is resistant or intolerant to a prior non-telomerase inhibitor-based therapy.

10. A method for reducing bone marrow fibrosis in an individual diagnosed with or suspected of having myelofibrosis (MF) or myelodysplastic syndrome, the method comprising: administering a clinically effective amount of a telomerase inhibitor to the individual, wherein administration of the telomerase inhibitor reduces bone marrow fibrosis in the individual.

11. The method of claim 6 , wherein the telomerase inhibitor comprises an oligonucleotide.

12. The method of claim 11 , wherein the oligonucleotide is complementary to the RNA component of telomerase.

13. The method of claim 11 , wherein the oligonucleotide is 10-20 bases in length.

14. The method of claim 11 , wherein the oligonucleotide comprises the sequence TAGGGTTAGACAA (SEQ ID NO:12).

15. The method of claim 11 , wherein the oligonucleotide comprises at least one N3′→P5′ thiophosphoramidate internucleoside linkage.

16. The method of claim 15 , wherein the oligonucleotide comprises N3′→P5′ thiophosphoramidate internucleoside linkages.

17. The method of claim 11 , wherein the oligonucleotide further comprises a lipid moiety linked to the 5′ and/or 3′ end of the oligonucleotide.

18. The method of claim 17 , wherein the lipid moiety is linked to the 5′ and/or 3′ end of the oligonucleotide via a linker.

19. The method of claim 18 , wherein the linker is a glycerol or aminoglycerol linker.

20. The method of claim 18 , wherein the lipid moiety is a palmitoyl (C16) moiety.

21. The method of claim 6 , wherein the telomerase inhibitor is imetelstat.

22. The method of claim 6 , wherein the telomerase inhibitor is administered with a pharmaceutically acceptable excipient.

23. The method of claim 6 , wherein the telomerase inhibitor is formulated for oral, intravenous, subcutaneous, intramuscular, topical, intraperitoneal, intranasal, inhalation, or intraocular administration.

24. The method of claim 6 , wherein administration of the therapeutically effective amount of the telomerase inhibitor comprises contacting one or more neoplastic progenitor cells with the telomerase inhibitor.

25. The method of claim 21 , wherein the effective amount of a telomerase inhibitor is 7.5 mg/kg to 9.3 mg/kg.

26. The method of claim 21 , wherein the effective amount of a telomerase inhibitor is 9.5 mg/kg to 11.7 mg/kg.

27. The method of claim 6 , wherein administration of the telomerase inhibitor does not inhibit cytokine-dependent megakaryocyte growth.

28. The method of claim 6 , wherein the individual carries a V617F gain of function mutation in the Janus kinase 2 (JAK2) gene.

29. The method of claim 28 , wherein administration of the telomerase inhibitor decreases the percentage of JAK2 V617F allelic burden in the individual.

30. The method of claim 6 , wherein administration of the telomerase inhibitor inhibits cytokine-independent megakaryocyte growth.

31. The method of claim 6 , wherein administration of the telomerase inhibitor inhibits CFU-mega.

32. The method of claim 31 , wherein inhibition of CFU-Mega is independent of reduction in JAK2 allelic burden.

33. The method of claim 1 , wherein the telomerase inhibitor comprises an oligonucleotide with the following characteristics:
(a) 10-20 bases in length;
(b) complementary to the RNA component of telomerase; and
(c) comprises at least one N3′→P5′ thiophosphoramidate internucleoside linkage.

34. The method of claim 33 , wherein the telomerase inhibitor further comprises a lipid moiety linked to the 5′ and/or 3′ end of the oligonucleotide.

35. The method of claim 34 , wherein the lipid moiety is linked to the 5′ and/or 3′ end of the oligonucleotide via a linker.

36. The method of claim 35 , wherein the oligonucleotide comprises a lipid moiety linked to the 5′ end of the oligonucleotide via an aminoglycerol linker.

37. The method of claim 36 , wherein the lipid moiety is a palmitoyl (C16) moiety.

38. The method of claim 37 , wherein the lipid moiety is linked to the 5′ end of the oligonucleotide via an aminoglycerol linker and a 5′-thiophosphate group.

39. The method of claim 33 , wherein the oligonucleotide comprises the sequence TAGGGTTAGACAA (SEQ ID NO:12).

40. The method of claim 6 , wherein the telomerase inhibitor comprises an oligonucleotide with the following characteristics:
(a) 10-20 bases in length;
(b) complementary to the RNA component of telomerase; and
(c) comprises at least one N3′→P5′ thiophosphoramidate internucleoside linkage.

41. The method of claim 40 , wherein the telomerase inhibitor further comprises a lipid moiety linked to the 5′ and/or 3′ end of the oligonucleotide.

42. The method of claim 41 , wherein the lipid moiety is linked to the 5′ and/or 3′ end of the oligonucleotide via a linker.

43. The method of claim 42 , wherein the oligonucleotide comprises a lipid moiety linked to the 5′ end of the oligonucleotide via an aminoglycerol linker.

44. Th

Assignees

• Geron Corp

Inventors

• Stuart Monic J
• Kelsey Stephen

Classifications

• A61K47/549

  Sugars, nucleosides, nucleotides or nucleic acids · CPC title

• A61K49/0423

  Nanoparticles, nanobeads, nanospheres, nanocapsules, i.e. having a size or diameter smaller than 1 micrometer · CPC title

• C12N2320/30

  Special therapeutic applications · CPC title

• B82Y5/00 Primary

  Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title

• C12N15/1135 Primary

  against oncogenes or tumor suppressor genes · CPC title