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Single Ascending Oral Dose Study to Investigate the Effects of OCT461201 in Healthy Volunteers - Trial NCT06398925

Access comprehensive clinical trial information for NCT06398925 through Pure Global AI's free database. This Phase 1 trial is sponsored by Oxford Cannabinoid Technologies Holdings PLC and is currently Completed. The study focuses on Healthy. Target enrollment is 32 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06398925
Phase 1
Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06398925
View on ClinicalTrials.gov
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Single Ascending Oral Dose Study to Investigate the Effects of OCT461201 in Healthy Volunteers
A Phase I, First-in-human, Randomised, Double-blind, Placebo-controlled, Single Ascending Oral Dose, Safety, Tolerability and Pharmacokinetic Study to Investigate the Effects of OCT461201 in Healthy Volunteers

Study Focus

Healthy

OCT461201 50 mg

Interventional

drug

Sponsor & Location

Oxford Cannabinoid Technologies Holdings PLC

Merthyr Tydfil, United Kingdom

Timeline & Enrollment

Phase 1

Jul 26, 2023

Sep 25, 2023

32 participants

Primary Outcome

Number of Participants with Treatment Emergent Adverse Events during the study assessed as mild, moderate or severe

Summary

A study in healthy volunteers to evaluate the safety, tolerability and pharmacokinetics of
 OCT461201. The study included a screening period, a single dose of study treatment or placebo
 and a follow up period.

ICD-10 Classifications

Obesity
Seeking and accepting physical, nutritional and chemical interventions known to be hazardous and harmful
Healthy person accompanying sick person
Lifestyle-related condition
Malnutrition

Data Source

ClinicalTrials.gov

NCT06398925

Non-Device Trial