Trials / Completed
CompletedNCT05881785
Study of Efficacy and Safety of GR1501 in Patients with Radiographic Axial Spondyloarthritis
A Randomized, Double-blind, Placebo-controlled, Phase III Study of Efficacy and Safety of GR1501 in Patients with Radiographic Axial Spondyloarthritis
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 465 (actual)
- Sponsor
- Genrix (Shanghai) Biopharmaceutical Co., Ltd. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this trial is to demonstrate the clinical efficacy of GR1501 at week 16; and to demonstrate safety and tolerability of GR1501 compared to placebo in patients with Radiographic Axial Spondyloarthritis at week 16 and long term safety up to Week 48。 The main question it aims to answer is whether GR1501 injection was superior to placebo in the proportion of subjects with ASAS20 response at week 16 in patients with Radiographic Axial Spondyloarthritis.
Detailed description
This is a randomized, double-blind, placebo-controlled, multicenter clinical study to evaluate the efficacy and safety of GR1501 injection in Radiographic Axial Spondyloarthritis, as well as a confirmatory clinical trial of immunogenicity. This clinical trial was divided into four stages, namely screening period (W-4\~W0), core treatment period (W0\~W16), maintenance treatment period (W16\~W32), and follow-up period (W32\~W48). target population: radiographic axial spondyloarthritis who had a inadequate response to NSAIDs or have a history of intolerance to NSAIDs. primary outcome measure:percentage of participants achieving an ASAS20 response in week 16.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | GR1501 low dose | 3×low dose GR1501 every 2 weeks,then low dose GR1501 monthly |
| BIOLOGICAL | GR1501 high dose | 3×high dose GR1501 every 2 weeks,then high dose GR1501 monthly |
| BIOLOGICAL | placebo | * Core treatment period:placebo * Maintenance treatment period: GR1501 injection |
Timeline
- Start date
- 2022-06-13
- Primary completion
- 2023-12-18
- Completion
- 2024-05-21
- First posted
- 2023-05-31
- Last updated
- 2024-09-25
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05881785. Inclusion in this directory is not an endorsement.