Osteoarthritis

Therapeutic subtypes of knee osteoarthritis: differential treatment effects among predicted endotypes in past clinical trials

Arthritis Res TherPublished Secondary analysis of randomised trials

Authors' conclusion

This exploratory study suggests the feasibility of predicting KOA endotypes using a minimal panel of tissue-turnover biomarkers.

Study context

Population
Knee osteoarthritis (KOA) participants from IMI-APPROACH (model development) and from the randomised placebo-controlled trials MIV-711, salmon calcitonin and UBX0101226 IMI-APPROACH
Comparison
Treatment effects across predicted biomarker-based endotypes (structural damage, inflammation, low tissue turnover) in prior KOA drug trials
Methodological detailsexploratory, hypothesis-generating biomarker endotyping study, multinomial logistic regression, post hoc analysis of randomised placebo-controlled trials
  • Exploratory, hypothesis-generating biomarker endotyping study
  • Multinomial logistic regression
  • Post hoc analysis of randomised placebo-controlled trials

Primary result

As reported in the abstract

Treatment effect by predicted endotype

Structural damage endotype: 26-week reduction in NRS knee pain with MIV-711 (greatest numerical reduction), 95% CI −16.23%, 3.31%

−6.46%

Structural damage endotype (only endotype significant): 2-year reduction in WOMAC pain with salmon calcitonin, 95% CI −10.55%, −1.83%

−6.19%

Further findings

SD of 2-year change in WOMAC pain, top 20% probability of structural damage endotype, salmon calcitonin

Reduction in SD of 2-year change in WOMAC pain
9-15%
Potential reduction in needed sample size with enrichment
18-28%

Original publication

Therapeutic subtypes of knee osteoarthritis: differential treatment effects among predicted endotypes in past clinical trials. Arthritis Res Ther. Published 7 May 2026. doi:10.1186/s13075-026-03825-7

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.