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 I Study Evaluating the Safety, Tolerability, and Pharmacokinetics of VVN432 Nasal Spray

The goal of this clinical study is to evaluate the safety, tolerability, and pharmacokinetics (PK) of VVN432 Nasal Spray in healthy volunteers (Phase Ia) and in patients with chronic rhinosinusitis (Phase 1b). This study consists of two parts (Phase 1a and Phase 1b): Phase 1a (SAD) is a single-center, randomized, double-masked, vehicle-controlled study to assess the safety, tolerability, and PK of VVN432 Nasal Spray in healthy adult subjects. Phase 1b (MAD) is a multi-center, randomized, double-masked, vehicle-controlled study to assess the safety, tolerability, PK/PD, and preliminary efficacy of VVN432 Nasal Spray in patients with chronic rhinosinusitis.

Participants needed: 60
Trial details
Phase: Phase 1Age: 18-55Biological sex: AllType: InterventionalSponsor: VivaVision Biotech, IncUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

Healthy male or female subjects aged 18 to 55 years old (inclusive); [+8]

Known hypersensitivity or contraindications to the study drug or its components; [+8]

Status: Not yet recruiting

A Phase 3 Study of VVN461 Ophthalmic Solution for Noninfectious Anterior Uveitis

This is a multicenter, randomized, single-masked, active-controlled, parallel, Phase III pivotal study in China

Participants needed: 152
Trial details
Phase: Phase 3Age: 18-70Biological sex: AllType: InterventionalSponsor: VivaVision Biotech, IncUpdated: Aug 22, 2025
Eligibility criteria

At the time of signing the informed consent form (ICF), the subject must be aged... [+3]

At screening, the affected eye has an ACC grade of 4+ or hypopyon [+1]

Status: Recruiting

Study of 5% VVN001 Ophthalmic Solution in Dry Eye Disease

This is a Phase 3, randomized, double-Masked, vehicle-controlled, multi-center study designed to evaluate the safety and efficacy of 5% VVN001 Ophthalmic Solution versus vehicle in Chinese subjects with dry eye disease.

Participants needed: 700
Trial details
Phase: Phase 3Age: 30-80Biological sex: AllType: InterventionalSponsor: VivaVision Biotech, IncUpdated: Nov 20, 2024Locations: 1
Eligibility criteria

Provided written informed consent prior to any study-related procedures. [+6]

Have a known hypersensitivity or contraindication to the IP or components of IP. [+2]