Fact CheckerSign in

NCT07349329Not yet recruitingPhase 3

A Study to Evaluate the Efficacy and Safty of 608 in Patients With Non- Radiographic Axial Spondyloarthritis (Nr-axSpA)

A Multicenter, Randomized, Double-blind, Placebo-controlled, Phase III Clinical Study to Evaluate the Efficacy and Safety of 608 in Patients With Non-radiographic Axial Spondyloarthritis (Nr-axSpA)

Source: ClinicalTrials.gov · Last updated 16 Jan 2026

Brief summary (registry, in English)

This study will evaluate the efficacy and safety of 608 in patients with nr-axSpA.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
380 (estimated)
First submitted
9 Jan 2026
Start date
9 Mar 2026
Primary completion date
19 Apr 2028
Lead sponsor
Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd.
NCT number
NCT07349329

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 380
  • From 9 Mar 2026 to the primary completion date, 19 Apr 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with other uncontrolled active inflammatory diseases.
  • Patients who have active Hepatitis B, Hepatitis C or HIV infections as determined by positive results at Screening.
  • History of cancer.
  • Known or suspected history of immunosuppression.
  • Known with allergic or intolerant to mometasone furoate spray or 608/placebo.

Lab values

  • Clinical laboratory tests and other tests that reveal abnormalities with clinical significance

Who the study is looking for

  • Female and male patients at least 18 years of age at the time of screening.
  • Diagnosis of axial spondyloarthritis according to Ankylosing Spondylo Arthritis International Society (ASAS) axial spondyloarthritis criteria
  • Objective signs of inflammation (magnetic resonance imaging (MRI) or abnormal C-reactive protein)
  • Total back pain as measured by NRS ≥ 4 at baseline

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.