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 Clinical Study to Evaluate the Efficacy, Safety, and Tolerability of Plonmarlimab in Subjects With Relapsed/Refractory Rheumatic and Immunologic Disease-associated Haemophagocytic Lymphohistiocytosis (Also Known as Macrophage Activation Syndrome [MAS])

A study designed to evaluate the efficacy, safety, immunogenicity, PK, and PD characteristics of Plonmarlimab in patients with relapsed/refractory rheumatic and immunologic disease-associated MAS, and to explore biomarkers related to the efficacy of Plonmarlimab.

Participants needed: 30
Trial details
Phase: Phase 3Age: 16-80Biological sex: AllType: InterventionalSponsor: TJ Biopharma Co., Ltd.Updated: Jul 20, 2026Locations: 18
Eligibility criteria

Age: 16 to 80 years (inclusive), of any gender. [+4]

Confirmed or suspected primary haemophagocytic lymphohistiocytosis (pHLH). [+16]

Status: Not yet recruiting

A Phase I Study to Evaluate the Safety,Pharmacokinetics,Pharmacodynamics,and Efficacy of TJ037130 in Adult Participants With Advanced Solid Tumors

The goal of this clinical trial is to evaluate the safety and tolerability of TJ037130 in participants with advanced or metastatic solid tumors, and to determine the Potential Optimal Biological Dose (POBD) of TJ037130 for subsequent investigations.

Participants needed: 128
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: TJ Biopharma Co., Ltd.Updated: Jul 20, 2026Locations: 1
Eligibility criteria

Males or females aged 18 years or older; [+9]

Prior exposure to CLDN6-targeted therapy; [+3]

Status: Recruiting

A Study to Evaluate the Efficacy,Safety,Tolerability,Pharmacokinetics,and Immunogenicty of Plonmarlimab in Subjects With Acute Gouty Arthritis

This is a multi center,randomized,double-blind,double-dummy,active-controlled study,and planned enrollment of 120-170 subjects,an interim analysis will be conducted after first 60 subjects complete the 72 -hour pain Visual Analogue Scale(VAS) assessment following their initial dose.Based on the analysis result,the sample size may be adjusted, and 1or 2 group(s)of the investigational drug will be selected to continue enrollment along with the active comparator group.The goal is to evaluate the efficacy of plonmarlimab in subjects with acute gouty arthristis.

Participants needed: 170
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: TJ Biopharma Co., Ltd.Updated: Apr 3, 2026Locations: 1
Eligibility criteria

Subjects aged ≥18 years, regardless of gender. [+8]

Secondary gout caused by various etiologies (e.g., gout induced by chemotherapy,... [+18]