KH607
/ Chengdu Kanghong Pharma
- LARVOL DELTA
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August 04, 2026
A Study of KH607 as Monotherpy in Adults Participants With Major Depressive Disorder
(clinicaltrials.gov)
- P3 | N=232 | Not yet recruiting | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.
New P3 trial • CNS Disorders • Depression • Major Depressive Disorder • Mood Disorders • Psychiatry
July 29, 2026
A Phase 2 Study to Evaluate Efficacy and Safety of KH607 Tablets in Adult Participents With Major Depressive Disorder
(clinicaltrials.gov)
- P2 | N=126 | Completed | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd. | Not yet recruiting ➔ Completed
Trial completion • CNS Disorders • Depression • Major Depressive Disorder • Mood Disorders • Psychiatry
July 29, 2026
A Phase 2 Study to Evaluate Efficacy and Safety of KH607 Tablets in Woman With Postpartum Depression
(clinicaltrials.gov)
- P2 | N=72 | Completed | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd. | Not yet recruiting ➔ Completed | Trial completion date: Apr 2027 ➔ Apr 2026 | Trial primary completion date: Jan 2027 ➔ Apr 2026
Trial completion • Trial completion date • Trial primary completion date • CNS Disorders • Depression • Mood Disorders • Postpartum Depression • Psychiatry
August 04, 2026
Compare the Efficacy and Safety of KH607 Tablets Versus Vortioxetine Hydrobromide Tablets in Adult Patients With Major Depressive Disorder
(clinicaltrials.gov)
- P3 | N=326 | Not yet recruiting | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.
New P3 trial • CNS Disorders • Depression • Major Depressive Disorder • Mood Disorders • Psychiatry
July 03, 2026
A Phase 2 Study to Evaluate Efficacy and Safety of KH607 Tablets in Adult Participents With Major Depressive Disorder
(clinicaltrials.gov)
- P2 | N=120 | Completed | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd. | Recruiting ➔ Completed
Trial completion • CNS Disorders • Depression • Major Depressive Disorder • Mood Disorders • Psychiatry
June 10, 2026
A Study to Evaluate the Effect of Food on the Pharmacokinetic Characteristics and Safety Profile of KH607 in Healthy Chinese Participants
(clinicaltrials.gov)
- P1 | N=16 | Not yet recruiting | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.
New P1 trial
July 31, 2025
A Phase 2 Study to Evaluate Efficacy and Safety of KH607 Tablets in Woman With Postpartum Depression
(clinicaltrials.gov)
- P2 | N=72 | Not yet recruiting | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.
New P2 trial • CNS Disorders • Depression • Mood Disorders • Postpartum Depression • Psychiatry
August 05, 2025
A Phase 2 Study to Evaluate Efficacy and Safety of KH607 Tablets in Adult Participents With Major Depressive Disorder
(clinicaltrials.gov)
- P2 | N=120 | Not yet recruiting | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.
New P2 trial • CNS Disorders • Depression • Major Depressive Disorder • Mood Disorders • Psychiatry
May 26, 2025
The Discovery and Development of KH607 as a Treatment for Postpartum Depression (PPD) and Major Depressive Disorder (MDD)
(APA 2025)
- "Phase II clinical studies are currently ongoing. We expect that the compound to be developed as a new treatment to address the unmet medical needs for PPD and MDD patients."
CNS Disorders • Depression • Major Depressive Disorder • Mood Disorders • Postpartum Depression • Psychiatry
May 01, 2024
Phase 1 Study of KH607 Tablets
(clinicaltrials.gov)
- P1 | N=88 | Recruiting | Sponsor: Chengdu Kanghong Pharmaceutical Group Co., Ltd.
New P1 trial
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