Clinical trials

8

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 Clinical Study to Evaluate the Efficacy and Safety of Bempedoic Acid

This trial is a multicenter randomized, double-blind, placebo-controlled phase III study to evaluate the efficacy and safety of Bempedoic Acid Tablets in patients with hyperlipidemia not adequately controlled by Statins.

Participants needed: 222
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Jun 3, 2026
Eligibility criteria

For participants with high risk of ASCVD: LDL-C ≥ 2.6 mmol/L (or 100 mg/dL); [+1]

Known allergy to any component of the investigational drug or its excipients or... [+8]

Status: Not yet recruiting

Study Evaluating the Safety, Efficacy and Pharmacokinetics of SYH9089 Injection in Patients Undergoing Abdominal Surgery.

This is a randomized, double-blind, active drug- and placebo-controlled, dose-escalation clinical study conducted in patients scheduled to undergo abdominal surgery. It aims to evaluate the tolerability, safety, pharmacokinetics, and efficacy of SYH9089 Injection for postoperative analgesia in these patients.

Participants needed: 60
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Apr 9, 2026
Eligibility criteria

1. Fully understand the purpose and significance of this study, voluntarily part...

Patientss with poorly controlled blood pressure despite medication: systolic blo... [+7]

Status: Not yet recruiting

Study to Evaluate Safety and Efficacy of SYHX1901 Tablets in Severe Alopecia Areata Patients

The purpose of this study is to evaluate the efficacy and safety of different doses of SYHX1901 tablets in the treatment of severe alopecia areata.

Participants needed: 156
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Jun 3, 2025
Eligibility criteria

Subjects fully understand and voluntarily participate in this study and sign inf... [+5]

Participants who have received hair implants; [+22]

Status: Not yet recruiting

A Phase III Study of SYHX1901 Tablets in the Treatment of Moderate to Severe Plaque Psoriasis

The purpose of this study is to evaluate the efficacy and safety of different doses of SYHX1901 tablets in the treatment of moderate to severe plaque psoriasis.

Participants needed: 500
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Apr 30, 2025
Eligibility criteria

Subject must be diagnosed of chronic plaque psoriasis with no morphological chan... [+3]

Forms of psoriasis other than plaque psoriasis (Guttate psoriasis、erythrodermic... [+6]

Status: Recruiting

A Trial of Dextromethorphan and Bupropion Sustained-Release Tablets in Patients With Major Depressive Disorder

A multicenter, randomized, double-blind, placebo-controlled, phase 3 trial, aim to evaluate the efficacy and safety of dextromethorphan and bupropion sustained-release tablets in Chinese adult patients with major depressive disorder.

Participants needed: 388
Trial details
Phase: Phase 3Age: 18-65Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: May 6, 2025Locations: 1
Eligibility criteria

Male or female, Age 18 - 65, inclusive [+6]

1. The researchers determined that it was refractory depression [defined as in a...

Status: Not yet recruiting

Liposomal Irinotecan in Combination With Oxaliplatin and S-1 Versus Gemcitabine Combined With Capecitabine as Postoperative Adjuvant Therapy for Pancreatic Cancer

This study will evaluate the efficacy and safety of adjuvant therapy with liposomal irinotecan in combination with oxaliplatin, and S-1 compared with capecitabine combined with capecitabine in participants with pancreatic ductal adenocarcinoma after radical surgery.

Participants needed: 408
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Aug 27, 2024
Eligibility criteria

Patients able and willing to provide a written informed consent aged 18-75 years... [+5]

Patients with other types of non-ductal tumor of the pancreas, including endocri... [+8]

Status: Recruiting

A Study to Evaluate the Efficacy and Safety of SYHX1901 Tablet in Non-segmental Vitiligo Patients

A 52-Week Study of SYHX1901 tablet in Adults with non-segmental vitiligo.

Participants needed: 144
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Jul 22, 2024Locations: 1
Eligibility criteria

Willing to sign an ICF, able to comprehend and comply with the study procedures. [+4]

Diagnosed as other active depigmentation disease. [+8]

Status: Not yet recruiting

A Study to Evaluate the Efficacy and Safety in Subjects With Advanced Breast Cancer Treated With SYHX2011

The main purpose of this study is to evaluate the efficacy and safety in subjects with advanced breast cancer treated with SYHX2011

Participants needed: 80
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: CSPC Ouyi Pharmaceutical Co., Ltd.Updated: Apr 9, 2024Locations: 1
Eligibility criteria

1.Voluntarily sign the written informed consent and willing to cooperate with th... [+9]

1. History of severe allergy or major hypersensitivity to paclitaxel or human se... [+18]