IP Library Patent Application 17871180
Patent Application
App. No. 17/871,180

METHODS OF STIMULATING BONE GROWTH WITH ABALOPARATIDE AND DENOSUMAB

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Quick Facts
Patent No.
US None
App. No.
17/871,180
Abstract

Provided herein are methods for increasing bone mineral density, treating osteoporosis and the like, that include administration of abaloparatide in combination with denosumab.

Claims (30)

1 - 21 . (canceled)

22 . A method of increasing bone mineral density in a subject in need thereof, comprising administering to said subject:

a first amount of abaloparatide; and

a second amount of denosumab,

wherein bone mineral density is increased in the subject in response to administration of abaloparatide and denosumab.

23 . The method according to claim 22 , wherein the first amount of abaloparatide is 80 mcg daily administered subcutaneously or 300 mcg daily administered transdermally.

24 . The method according to claim 22 , wherein the second amount of denosumab is 60 mg administered subcutaneously every six months.

25 . The method according to claim 22 , wherein the abaloparatide is administered concomitantly with the administration of denosumab.

26 . The method according to claim 22 , wherein the abaloparatide is administered before administration of denosumab.

27 . The method according to claim 22 , wherein the denosumab is administered before administration of abaloparatide.

28 . The method according to claim 22 , wherein a total hip BMD is increased at least 10% in subjects where abaloparatide is administered with ongoing treatment with denosumab for 18 months.

29 . The method according to claim 22 , wherein a total spine BMD is increased at least 15% in subjects where abaloparatide is administered with ongoing treatment with denosumab for 18 months.

30 . The method according to claim 22 , wherein denosumab and abaloparatide are administered at the onset of treatment, with abaloparatide treatment being initiated at a time of a first dose of denosumab, or within a period of one month of a first dose of denosumab.

31 . The method according to claim 22 , wherein denosumab is administered at the onset of treatment and abaloparatide treatment is initiated at least 6 months after initial treatment with denosumab.

32 . The method according to claim 22 , wherein abaloparatide is administered at the onset of treatment and denosumab treatment is initiated at least one month after treatment with abaloparatide is initiated.

33 . A method of treating osteoporosis in a subject in need thereof, comprising administering to said subject:

a first amount of abaloparatide; and

a second amount of denosumab,

wherein the osteoporosis is treated in the subject in response to administration of abaloparatide and denosumab.

34 . A method of treating denosumab-refractory osteoporosis, the method comprising:

administering an effective amount of abaloparatide to a subject having denosumab-refractory osteoporosis,

wherein administration of an effective amount of abaloparatide to the subject increases bone formation in the subject without increasing bone resorption.

35 . The method according to claim 34 , wherein abaloparatide is administered in combination with denosumab treatment.

36 . The method according to claim 34 , wherein denosumab treatment is discontinued when abaloparatide treatment is initiated.

37 . The method according to claim 36 , wherein abaloparatide treatment is initiated within one month after treatment with denosumab is discontinued.

38 . The method according to claim 34 , wherein abaloparatide treatment is initiated within three months of an anticipated last dose of denosumab.

39 . The method according to claim 34 , wherein administration of an effective amount of abaloparatide to the subject increases the subject's lumbar spine BMD or hip BMD relative to treatment with denosumab alone.

40 . The method according to claim 34 , wherein a total hip BMD is increased at least 10% after 18 months of administration of abaloparatide.

41 . The method according to claim 34 , wherein the subject is a subject at high risk for a fracture despite denosumab treatment, as indicated by declining or persistently low bone mass density.

42 . The method according to claim 34 , wherein the subject has had denosumab therapy, followed by teriparatide therapy, and has a total hip BMD below baseline at the start of teriparatide therapy.

Assignments (3)
PATENT SECURITY AGREEMENT Recorded Mar 16, 2026
From: RADIUS HEALTH, INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 075104/0121 →
RELEASE OF SECURITY INTEREST Recorded Oct 30, 2025
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: RADIUS HEALTH, INC.
Reel/Frame 073278/0396 →
SECURITY INTEREST Recorded Aug 16, 2022
From: RADIUS HEALTH, INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 061179/0001 →