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MT-201

Phase 1

Healthy Volunteer | Small molecule | Other |cbdMD, Inc.|Last Updated: Aug 21, 2026

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLED
Total Trials1
Total Enrollment25

FDA Designations

No designations recorded

Clinical trial landscape

MT-201 · 1 trial · 1 indication

Phase 1 1
NCT07776782A Single-Dose Study of MT-201 and Concomitant Infliximab in Healthy ParticipantsHealthy Volunteer
RECRUITING25 Analytics
PHASE1RECRUITING
A Single-Dose Study of MT-201 and Concomitant Infliximab in Healthy Participants
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Study Endpoints

Primary Endpoints

Number of Participants with non-SAEs and SAES
Up to 8 weeks post dose

Incidence of adverse events, clinically significant laboratory abnormalities, clinically significant electrocardiogram, vital signs, and physical examination abnormalities.

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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeOTHER

Treatment Arms

ArmTypeDescription
Single Dose of MT-201 and Concomitant InfliximabEXPERIMENTALTo evaluate the safety and tolerability of single doses of MT-201 and Concomitant Infliximab

Interventions

NameTypeDescription
MT-201DRUGMT-201 and Infliximab
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Eligibility Criteria

Age Range19 Years to 55 Years
SexALL
Healthy VolunteersYes
Study Sites1

Inclusion Criteria: 1. Male or female (of non-childbearing potential only) between 19 and 55 years of age inclusive, at the time of signing informed consent. 2. Females must be of non-childbearing potential and must have undergone sterilization procedures, and have official documentation, at least ...

Countries:United States
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