Clinical trials

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

Condition / disease
Location
Status: Recruiting

A Phase III Study of CM326 in Subjects With Moderate to Severe Asthma

This study is a multi-center, randomized, double-blind, placebo-controlled Phase Ⅲ clinical study to evaluate the efficacy, safety, PK characteristics, PD effects and immunogenicity of CM326 in subjects with moderate to severe asthma. The study consists of three periods, including an up to 4-week screening period, a 52-week double-blind randomized treatment period, and a 12-week safety follow-up period.

Participants needed: 230
Trial details
Phase: Phase 3Age: 18-80Biological sex: AllType: InterventionalSponsor: CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.Updated: Apr 28, 2026Locations: 1
Eligibility criteria

Understand the study and voluntarily sign the informed consent form. [+9]

Chronic obstructive pulmonary disease (COPD) without asthma or other lung diseas... [+23]

Status: Not yet recruiting

A Comparative Pharmacokinetic Study of CM326 in Healthy Subjects

This is a randomized, open-label, parallel-controlled study to compare the PK, safety, and immunogenicity of CM326 administered via different delivery devices in healthy subjects.

Participants needed: 192
Trial details
Phase: Phase 1Age: 18-55Biological sex: MaleType: InterventionalSponsor: CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.Updated: Apr 30, 2026
Eligibility criteria

Participants [c1.1]must be informed of the study before it begins, fully underst... [+5]

History of chronic diseases or severe diseases involving the circulatory system,... [+18]

Status: Recruiting

The Safety, Tolerability, and Pharmacokinetics of of SYH9017 in Chinese Participants With Overweight and Obesity

This is a randomized, double-blind, single-center, dose-escalation, single ascending dose and multiple ascending dose study of SYH9017 in Chinese participants with overweight and obesity.

Participants needed: 66
Trial details
Phase: Phase 1Age: 18-60Biological sex: AllType: InterventionalSponsor: CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.Updated: Apr 6, 2026Locations: 1
Eligibility criteria

Chinese male or female adult participants aged 18-60 years (inclusive) with over... [+4]

A history of severe drug or food allergies, or any participant who is judged by... [+18]

Status: Not yet recruiting

A Randomized, Double-blind, Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of CM326 in Participants With Chronic Rhinosinusitis With Nasal Polyposis

This is a multi-center, randomized, double blind, placebo-controlled Phase III study to evaluate the efficacy and safety of CM326, and to observe the Pharmacokinetics, Pharmacodynamics and I immumogenicity\[c2.1\] of CM326 in patients with chronic rhinosinusitis with nasal polyps (CRSwNP).The study consists of four periods, including an up to 4-week screening/run-in period, a 24-week double-blind randomized treatment period, a 28-week open-label treatment period, and an 8-week safety follow-up period.

Participants needed: 212
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.Updated: Feb 19, 2026
Eligibility criteria

Understand the study and voluntarily sign the informed consent form. [+9]

Presence of nasal conditions affecting NPS evaluation, including but not limited... [+29]