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Proximod Pharmacokinetics In Healthy Subjects - Trial NCT06361186

Access comprehensive clinical trial information for NCT06361186 through Pure Global AI's free database. This Phase 1 trial is sponsored by Longevity Inc. and is currently Completed. The study focuses on Rheumatoid Arthritis. Target enrollment is 134 participants.

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NCT06361186
Phase 1
Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06361186
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Proximod Pharmacokinetics In Healthy Subjects
A Single-center, Randomized, Double-blind, Placebo-controlled Phase I Study to Evaluate the Tolerability, Pharmacokinetics and Pharmacodynamics of Proximod in Healthy Subjects.

Study Focus

Rheumatoid Arthritis

Proximod

Interventional

drug

Sponsor & Location

Longevity Inc.

Changchun, China

Timeline & Enrollment

Phase 1

Sep 14, 2017

Jun 22, 2021

134 participants

Primary Outcome

Peak plasma concentration (Cmax),Time to peak plasma concentration (Tmax),The lowest plasma concentration (Cmin),Half-life (t1/2),Number of adverse events and number of participants with adverse events

Summary

The goal of this clinical trial is to evaluate the tolerability, pharmacokinetics and
 pharmacodynamics of Proximod in healthy subjects. The main questions it arms to answer are:
 
 1. to evaluate the safety and tolerance of Proximod in healthy subjects after single or
 repeated doses.
 
 2. to learn the pharmacodynamics of Proximod in healthy subjects after single or repeated
 doses.
 
 3. to evaluation of the effect of food on the pharmacokinetics of Proximod in healthy
 subjects Participants will receive test tablets or placebo at the indicated date and
 collect blood samples.

ICD-10 Classifications

Rheumatoid arthritis, unspecified
Other rheumatoid arthritis
Other specified rheumatoid arthritis
Rheumatoid arthritis with involvement of other organs and systems
Seronegative rheumatoid arthritis

Data Source

ClinicalTrials.gov

NCT06361186

Non-Device Trial