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NCT05182034

Clinical Trial to Evaluate Efficacy and Safety of SMUP-IA-01 in Patients With Knee Osteoarthritis

Completed Phase 2 Last updated 5 February 2025
What this trial tests

Phase 2 trial testing SMUP-IA-01(low dose) in Knee Osteoarthritis in 94 participants. Completed in 17 October 2023.

Timeline
24 February 2022
Primary endpoint
17 October 2023
17 October 2023

Quick facts

Lead sponsorMedipost Co Ltd.
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment94
Start date24 February 2022
Primary completion17 October 2023
Estimated completion17 October 2023
Sites5 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Medipost Co Ltd. — full company profile →

Who can join

19 and older, any sex, with Knee Osteoarthritis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This clinical trial is for patients who have been diagnosed with Kellgren-Lawrence (K\&L) Grade 2 or 3 knee osteoarthritis on radiographic examination. Only subjects who voluntarily agree to participate by filling out the written Informed Consent document will undergo screening for subject selection (inclusion/exclusion) criteria, at which time the severity of OA in each knee will be used to determined which knee will be treated (index knee - i.e., the more severely affected knee), and enroll in this study.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Knee Osteoarthritis

Currently open trials in the same condition.

Other Medipost Co Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05182034.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing