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Not Yet RecruitingNCT07277933

Efficacy and Safety of KHN702 Tablets in Moderate to Severe Post-operative Pain Subjects

Efficacy and Safety of KHN702 Tablets in Moderate to Severe Post-operative Pain Patients: A Randomized, Double-blind, Placebo-Controlled, Phase Ib Trial

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Chengdu Kanghong Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study is a randomized, double-blind, placebo-controlled, parallel-group clinical trial. To preliminarily evaluate the safety and efficacy of KHN702 tablets in moderate to severe post-operative pain patients.

Conditions

Interventions

TypeNameDescription
DRUGKHN702KHN702 tablet for oral administration
DRUGKHN702 placeboKHN702 placebo tablet for oral administration

Timeline

Start date
2025-12-01
Primary completion
2026-02-01
Completion
2026-02-01
First posted
2025-12-11
Last updated
2025-12-11

Source: ClinicalTrials.gov record NCT07277933. Inclusion in this directory is not an endorsement.