US2017056499A1PendingUtilityA1
Solid oral form of a medicinal preparation and a method for the production thereof
Est. expiryMar 13, 2026(expired)· nominal 20-yr term from priority
Inventors:Oleg Iliich Epshtein
A61P 29/00A61P 25/30A61P 15/10A61K 9/2018C07K 16/40A61K 39/39591A61K 41/0004A61K 2039/505C07K 16/44C07K 16/241A61K 9/20A61K 39/395A61J 3/00
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Claims
Abstract
A solid dosage form of an antibody-based medicinal preparation comprising an effective amount of a carrier treated with a dilution containing at least one antibody to a biologically active molecule.
Claims
exact text as granted — not AI-modified1 .- 9 . (canceled)
10 . A solid dosage form for administration to a human subject, said dosage form comprising an effective amount of a pharmaceutically neutral carrier treated with a homeopathic dilution of an initial solution containing at least one antibody to a biologically-active molecule.
11 . The solid dosage form of claim 10 , wherein said initial solution is obtained by i) generating an immune response to said biologically-active molecule in a host external to said human subject thereby generating said antibody in said host, and ii) isolating said generated antibody from said host.
12 . The solid dosage form of claim 10 , wherein said biologically-active molecule is endogenous to said human subject.
13 . The solid dosage form of claim 12 , wherein said biologically-active molecule plays a role in regulation of pathological syndrome for said human.
14 . The solid dosage form of claim 12 , wherein said biologically-active molecule affects formation of pathological syndrome for said human.
15 . The solid dosage form of claim 10 , wherein said homeopathic dilution is prepared by successive dilutions.
16 . The solid dosage form of claim 15 , wherein said homeopathic dilution is prepared by combining said successive dilutions with external treatment.
17 . The solid dosage form of claim 16 , wherein said external treatment is mechanical shaking, ultrasonic treatment, or electromagnetic field treatment.
18 . The solid dosage form of claim 10 , wherein said carrier is lactose.
19 . The solid dosage form of claim 18 , which is in the form of a tablet.
20 . The solid dosage form of claim 19 , wherein said carrier comprises from 30% to 80% by weight with respect to total weight of said dosage form.
21 . The solid dosage form of claim 20 , further comprising a binder and a lubricant.
22 . The solid dosage form of claim 21 , wherein said lubricant comprises from 0.8% to 1.2% by weight with respect to total weight of said dosage form.
23 . The solid dosage form of claim 21 , wherein said binder comprises from 10% to 15% by weight with respect to total weight of said dosage form.
24 .- 28 . (canceled)
29 . The solid oral dosage form of claim 11 , wherein said isolating step provides an isolate containing said at least one antibody.
30 . The solid oral dosage form of claim 29 , wherein said initial solution contains 0.05 to 3% of said isolate.
31 . (canceled)Join the waitlist — get patent alerts
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