Granted Patent B2

US 12,527,786 · App. 17/890,133 · Granted Jan 20, 2026

Inventors: Peter Mack (Chapel Hill, NC); Timm Trenktrog (Binningen, CH); Dustin Melton (Melbane, NC); Bethany Amber Doty (Clayton, NC); Jon Schroeder (Madison, WI); Lisa Marie Garrett (Swindon, GB)

Assignee: Mind Medicine, Inc.

A61K31/48A61K9/0056A61K9/20A61K9/2013A61K9/2018A61K9/205A61K9/2054A61K9/2095A61K47/10A61K47/22A61K47/26A61K47/36A61K47/60A61K47/6923

Abstract

Claims (14)

1 . A composition of a solid oral immediate release formulation of LSD, consisting of LSD or a salt thereof contained within an immediate release dosage form of an orally disintegrating tablet, wherein said composition is produced by lyophilization of a single feedstock in a pre-formed mold to form the orally disintegrating tablet, wherein said feedstock consists of LSD or a salt thereof; a non-gelling matrix former of maltodextrin; a filler chosen from the group consisting of mannitol and trehalose; water; and 1-5% weight percent of a binder of hydroxypropyl methylcellulose, and wherein said LSD or salt thereof is present at less than 1% weight percent of said feedstock.

2 . A method of making a solid oral immediate release formulation of LSD, consisting of the steps of:

lyophilizing a single flash frozen stock solution consisting of LSD or a salt thereof and excipients of a non-gelling matrix former of maltodextrin, filler, water, 1-5% weight percent of a binder of hydroxypropyl methylcellulose, and buffer in a pre-formed mold; and

forming an orally disintegrating tablet, wherein the LSD or salt thereof is present at less than 1% weight percent of said stock solution.

3 . The method of claim 2 , wherein the filler is chosen from the group consisting of lactose, mannitol, dicalcium phosphate, calcium sulfate, starch, cellulose, kaolin, sodium chloride, sorbitol, trehalose, and sucrose.

4 . The method of claim 2 , wherein the buffer is chosen from the group consisting of citrate, phosphate, and acetate.

5 . The method of claim 2 , wherein the LSD is in a salt form and the salt is chosen from the group consisting of hydrochloride, hydrobromide, maleate, tartrate, citrate, phosphate, fumarate, sulfate, mesylate, acetate, and oxalate.

6 . A method of treating an individual, including the steps of:

administering a solid oral immediate release formulation of LSD of an orally disintegrating tablet, wherein the orally disintegrating tablet is produced by lyophilization of a single feedstock in a pre-formed mold to form the orally disintegrating tablet, wherein said feedstock consists of LSD or a salt thereof; a non-gelling matrix former of maltodextrin; a filler chosen from the group consisting of mannitol and trehalose; water; and 1-5% weight percent of a binder of hydroxypropyl methylcellulose, and wherein the LSD or salt thereof is present at less than 1% weight percent of said feedstock; and

treating the individual.

7 . The method of claim 6 wherein the individual has trouble swallowing, is elderly, or has dementia.

8 . The method of claim 6 , wherein said treating step is further defined as treating a condition or disease chosen from the group consisting of anxiety disorders, depression, headache disorder, obsessive compulsive disorder (OCD), personality disorders, stress disorders, drug disorders, gambling disorder, eating disorder, body dysmorphic disorder, pain, neurodegenerative disorders, autism spectrum disorder, eating disorders, and neurological disorders.

9 . The method of claim 6 , wherein the LSD is in a salt form and the salt is chosen from the group consisting of hydrochloride, hydrobromide, maleate, tartrate, citrate, phosphate, fumarate, sulfate, mesylate, acetate, and oxalate.

10 . The method of claim 6 , wherein said administering step is further defined as administering 0.01-1 mg of LSD or a salt thereof.

Assignments (4)

Continuity (2)

References Cited (400)