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NCT05829798

An Efficacy and Safety 6-months Study of SYNOLIS VA 80/160 and SYNOLIS VA 40/80 in the Treatment of Symptomatic Knee Osteoarthritis

Completed NA Last updated 26 April 2023
What this trial tests

NA trial testing SYNOLIS VA 80/160 in Osteoarthritis, Knee in 82 participants. Completed in 1 October 2021.

Timeline
14 January 2021
Primary endpoint
1 October 2021
1 October 2021

Quick facts

Lead sponsorAptissen SA
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment82
Start date14 January 2021
Primary completion1 October 2021
Estimated completion1 October 2021
Sites3 locations across Poland

Drugs / interventions tested

Conditions studied

Sponsor

Aptissen SA

Who can join

Adults 35 to 75, any sex, with Osteoarthritis, Knee. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Multicentre, independent assessment study on SYNOLIS VA 80/160 and SYNOLIS VA 40/80 over a period of 24 weeks

Publications & conference data

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

Verify or expand the search:

Other recruiting trials for Osteoarthritis, Knee

Currently open trials in the same condition.

Other Aptissen SA 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/NCT05829798.

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