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Food-effect Study of Ammoxetine Hydrochloride Enteric-coated Tablets

NCT07508501 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2026-04-02

No results posted yet for this study

Summary

This study is a single-center, randomized, open-label, two-period crossover design to evaluate the effect of food on the pharmacokinetic profile of ammoxetine hydrochloride enteric-coated tablets.

Conditions

  • Healthy Participants

Interventions

DRUG

Ammoxetine hydrochloride enteric-coated tablets

Single-dose of 40mg of ammoxetine hydrochloride enteric-coated tablets

DRUG

Ammoxetine hydrochloride enteric-coated tablets

Single-dose of 40 mg of ammoxetine hydrochloride enteric-coated tablets

Sponsors & Collaborators

  • CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-02-08
Primary Completion
2023-02-24
Completion
2023-04-04

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07508501 on ClinicalTrials.gov