Clinical trials

7

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Study of KH607 as Monotherpy in Adults Participants With Major Depressive Disorder

This trial includes a short-term study and a long-term study. The short-term study is a multicenter, randomized, double-blind, placebo-controlled parallel-group study with a 6-week duration. The long-term study is a multicenter, open-label, single-arm study with a maximum duration of 27 weeks.

Participants needed: 232
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Aug 3, 2026
Eligibility criteria

Age: 18 to 65 years old (inclusive), Male or female. [+8]

Other psychiatric disorders meeting DSM-5 criteria, including but not limited to... [+20]

Status: Not yet recruiting

Compare the Efficacy and Safety of KH607 Tablets Versus Vortioxetine Hydrobromide Tablets in Adult Patients With Major Depressive Disorder

This trial includes a short-term study and a long-term study. The short-term study is a multicenter, randomized, double-Blind, double-Dummy, Parallel-Controlled study with a 6-week duration. The long-term study is a withdrawal follow-up study; participants meeting relapse criteria may receive one cycle of KH607 Tablets treatment.

Participants needed: 326
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Aug 3, 2026
Eligibility criteria

Age: 18 to 65 years old (inclusive), Male or female. [+8]

Other psychiatric disorders meeting DSM-5 criteria, including but not limited to... [+22]

Status: Not yet recruiting

A Study to Evaluate the Effect of Food on the Pharmacokinetic Characteristics and Safety Profile of KH607 in Healthy Chinese Participants

This study is a randomized, open-label, 2-period, 2-sequence, crossover food-effect study designed to evaluate the effect of a high-fat meal on the pharmacokinetics of a single oral dose of KH607 tablets in healthy participants, as well as to assess the safety of a single oral dose of KH607 tablets administered under fasting and fed conditions in healthy participants.

Participants needed: 16
Trial details
Phase: Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Jun 9, 2026
Eligibility criteria

Participants must be healthy and aged ≥18 and <45 years at the time of screening... [+3]

Participants with known allergy to any ingredient of KH607; or those with a know... [+4]

Status: Not yet recruiting

A Phase 1 Study of KHN707 Tablets in Healthy Participants

This is a single-center, randomized, double-blind, placebo-controlled study . The objective is to evaluate the safety , tolerability and PK profile of KHN707 tablets in Chinese healthy participants.

Participants needed: 38
Trial details
Phase: Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Apr 29, 2026
Eligibility criteria

1.Age: 18 to 45 years old (inclusive), Male or female. [+3]

1. Participants with clinically significant abnormalities in physical examinatio... [+21]

Status: Not yet recruiting

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

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.

Participants needed: 24
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Dec 11, 2025
Eligibility criteria

Subjects between the ages of 18 and 75 years, inclusive. [+5]

Participants experiencing acute or chronic pain unrelated to the surgical site,... [+16]

Status: Not yet recruiting

A Phase 1 Study of KHN702 Tablets in Healthy Subjects

This study is a single-center, randomized, double-blind, placebo-controlled study divided into a Single Ascending Dose (SAD) stage and a Multiple Ascending Dose (MAD) phase. The primary objective is to evaluate the safety and tolerability of KHN702 tablets in Chinese healthy volunteers(HVs).

Participants needed: 84
Trial details
Phase: Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Jul 1, 2025
Eligibility criteria

Have clinically significant medical history or clinical manifestations, includin... [+21]

Status: Not yet recruiting

A Double-Blind, Randomized Comparative Study of Carliprazine and Aripiprazole in Patients with Acute Schizophrenia

This is a non-Inferiority trial to evaluate efficacy and safety of hydrochloride carliprazine capsules and aripiprazole tablets in treating acute schizophrenia in Chinese adults. 376 patients will be randomizdely assigned in a 1:1 ratio to treatment group and control group. All enrolled subjects will be orally administered with hydrochloride carliprazine capsules or aripiprazole tablets for 6 consecutive weeks.

Participants needed: 376
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.Updated: Sep 19, 2024
Eligibility criteria

Subjects between 18 and 65 years, male and female; [+5]

Other mental illnesses that meet DSM-5 criteria, excluding schizophrenia, includ... [+21]