US2021040192A1PendingUtilityA1
Method of promoting bone growth by an anti-actriia antibody
Est. expiryNov 23, 2025(expired)· nominal 20-yr term from priority
C07K 16/22A61K 38/00A61K 2039/505C12N 15/1136C12N 2310/11C07K 14/71A61P 19/08A61P 35/00C12N 15/1138A61K 38/179C07K 14/575A61K 39/3955A61K 45/06A61P 19/10C07K 2319/30A61P 35/04C07K 2317/76
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Claims
Abstract
In certain aspects, the present invention provides compositions and methods for promoting bone growth and increasing bone density.
Claims
exact text as granted — not AI-modified1 . A method for promoting bone growth, increasing bone density, or increasing bone strength, the method comprising administering to a subject in need thereof an effective amount of an anti-ActRIIa antibody.
2 . The method of claim 1 , wherein the anti-ActRIIa antibody is a monoclonal antibody.
3 . The method of claim 1 , wherein the anti-ActRIIa antibody is a humanized or fully human antibody.
4 . The method of claim 1 , wherein the method is for promoting bone growth in a subject in need thereof.
5 . The method of claim 1 , wherein the method is for increasing bone density in a subject in need thereof.
6 . The method of claim 1 , wherein the method is for increasing bone strength in a subject in need thereof.
7 . The method of claim 1 , wherein the method further comprises administering a second bone-active agent.
8 . The method of claim 7 , wherein the bone-active agent is selected from: a bisphosphonate, an estrogen, a selective estrogen-receptor modulator, a parathyroid hormone, a calcitonin, a calcium supplement, and a vitamin D supplement.
9 . A method for treating a bone-related disorder, the method comprising administering to a subject in need thereof an effective amount of an anti-ActRIIa antibody, wherein the bone-related disorder is associated with low bone density or decreased bone strength.
10 . The method of claim 9 , wherein the anti-ActRIIa antibody is a monoclonal antibody.
11 . The method of claim 9 , wherein the anti-ActRIIa antibody is a humanized or fully human antibody.
12 . The method of claim 9 , wherein the method further comprises administering a second bone-active agent.
13 . The method of claim 12 , wherein the bone-active agent is selected from: a bisphosphonate, an estrogen, a selective estrogen-receptor modulator, a parathyroid hormone, a calcitonin, a calcium supplement, and a vitamin D supplement.
14 . The method of claim 9 , wherein the bone-related disorder is primary osteoporosis.
15 . The method of claim 9 , wherein the bone-related disorder is post-menopausal osteoporosis.
16 . The method of claim 9 , wherein the bone-related disorder is secondary osteoporosis.
17 . The method of claim 9 , wherein the bone-related disorder is hypogonadal bone loss.
18 . The method of claim 9 , wherein the subject has a cancer that is associated with bone loss.
19 . The method of claim 9 , wherein the subject is the recipient of a cancer treatment regimen than is associated with bone loss.
20 . The method of claim 9 , wherein the bone-related disorder is bone metastases.
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