US2011105390A1PendingUtilityA1
Selection and treatment of patients suffering from wasting
Est. expiryOct 20, 2023(expired)· nominal 20-yr term from priority
A61P 43/00A61K 38/25A61P 21/00
42
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The invention relates to use of a GH secretagogue (e.g. GRF or an analog thereof) for increasing muscle function in a subject. Also disclosed herein are corresponding methods, packages and compositions.
Claims
exact text as granted — not AI-modified1 . A method for increasing muscle function and inhibiting the rate of onset or progression of severe wasting in a subject, wherein said severe wasting is defined as: (A) a body mass index less than or equal to 20; (B) a weight less than 90% of ideal body weight; (C) a fat free mass index less than or equal to 16 for a male; and/or (D) a fat free mass index less than or equal to 15 for a female, said method comprising administering an effective amount of (hexenoyl trans-3)hGRF(1-44)NH 2 (SEQ ID NO: 7) to said subject.
2 . The method of claim 1 , wherein said subject suffers from a condition selected from chronic obstructive pulmonary disease (COPD), chronic renal failure, congestive hear failure, human immunodeficiency virus infection, acquired immunodeficiency syndrome, cancer, malnutrition, frailty, immobilization paraplegia and spinal disorder
3 . The method of claim 1 , wherein said muscle function is selected from the group consisting of:
(a) muscle strength; (b) muscle endurance; and (c) both (a) and (b).
4 . The method of claim 3 , wherein said muscle function is muscle strength.
5 . The method of claim 4 , wherein said muscle strength is peripheral muscle strength.
6 . The method of claim 3 , wherein said muscle function is muscle endurance.
7 . The method of claim 1 , wherein said administering reduces a parameter selected from:
(a) breathing discomfort; (b) leg discomfort; and (c) both (a) and (b).
8 . The method of claim 1 , wherein said administering increases lean body mass in said subject.
9 . The method of claim 1 , wherein said administering decreases fat mass in said subject.
10 . The method of claim 1 , wherein said administering is through a route selected from intravenous, oral, transdermal, subcutaneous, mucosal, intramuscular, intranasal, intrapulmonary, parenteral, intrarectal and topical.
11 . The method of claim 1 , wherein said administering is through the subcutaneous route.
12 . The method of claim 1 , wherein said administering is at a dose from about 0.0001 mg to about 4 mg.
13 . The method of claim 12 , wherein said administering is at a dose selected from about 1 mg and about 2 mg.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.