A new vessel for an ancient medicine.
Oral DMT needs a a monoamine oxidase inhibitor (MAOI). The right MAOI can make all the difference.
The only clinically-available MAOIs in the United States have strict dietary requirements. Otherwise, these drugs can cause dangerously high blood pressure.
Reversible inhibitors of MAO-A (RIMAs) are selective for MAO-A versus MAO-B and are generally considered safer. Plant-sourced harmine and harmaline are RIMAs consumed alongside DMT in traditional ayahuasca ceremonies. However, harmine and harmaline exert off-target effects including gastrointenstinal distress and Parkinsonian-like tremors.
Moclobemide is a RIMA approved for clinical use in some countries, but it is not available in the United States. Moreover, it demonstrates relatively low potency at MAO-A and still exerts some degree of MAO-B inhibition. Low potency limits potential combination with DMT into a single formulation.
Remedi Therapeutics has identified a well-characterized, ultraselective, and potent MAOI that lacks hyperintensive risk, gastrointestinal symptoms, or tremors.
Reversible
Inhibits brain MAO-A with near return to baseline at 12 hours.
Selective & Potent
100x more potent than moclobemide.
No MAO-B activity.
Safe
No hypertensive crises in humans.
No need for dietary restrictions.
Opportunity
Path to first clinically available oral DMT
Macrodosing (experiential) and chronic microdosing (subhallucinogenic) strategies
Tailored formulations and pharmacokinetics depending on clinical indication
Intellectual property covering combinations with DMT and other tryptamines metabolized by MAO-A
MAOI has been tested in 450 subjects in Phase 1 and 2 Trials; excellent safety profile.