Stable cannabinoid formulations
The present invention is generally directed to substantially pure cannabidiol, stable cannabinoid pharmaceutical formulations, and methods of their use.
1. A method of treating Prader-Willi syndrome in a subject in need of such treatment, comprising administering to the subject an effective amount of an oral pharmaceutical formulation consisting of:
from about 8% to about 32% w/w cannabidiol;
caprylic/capric triglyceride at a concentration of 58 to 90% w/w;
alpha tocopherol at a concentration of from 0.01 to 1% w/w;
a sweetener at a concentration of 0.01 to 2% w/w; and
a flavoring agent at a concentration of 0.01 to about 1% w/w,
wherein w/w denotes weight by weight of the formulation, and wherein the effective amount results in administration of from about 20 to about 40 milligrams of cannabidiol per kilogram body weight of the subject per day, and wherein the subject is a human subject.
2. The method of claim 1 , wherein the method involves treating one or more symptoms of Prader-Willi syndrome.
3. The method of claim 2 , wherein the one or more symptoms of Prader-Willi syndrome is hyperphagia.
4. The method of claim 1 , wherein the human subject is a pediatric subject.
5. The method of claim 1 , wherein the dose of the cannabidiol is about 40 milligrams of cannabidiol per kilogram body weight of the subject per day.
6. The method of claim 1 , wherein the cannabidiol is greater than 98% pure.
7. The method of claim 1 , wherein the cannabidiol is synthetic cannabidiol.
8. The method of claim 1 , wherein the oral pharmaceutical formulation consists of:
10.53% w/w of cannabidiol;
88.945% w/w of caprylic/capric triglyceride;
0.2% w/w of alpha tocopherol;
0.025% w/w of sweetener; and
0.3% w/w of flavoring agent.
9. The method of claim 1 , wherein the oral pharmaceutical formulation consists of:
31.09% w/w of cannabidiol;
68.385% w/w of caprylic/capric triglyceride;
0.2% w/w of alpha tocopherol;
0.025% w/w of sweetener; and
0.3% w/w of flavoring agent.