Turn Therapeutics (TTRX) Stifel 2026 Virtual Immunology and Inflammation Forum summary
Event summary combining transcript, slides, and related documents.
Stifel 2026 Virtual Immunology and Inflammation Forum summary
23 Sep, 2026Trial enrichment strategies and regulatory impact
Enrichment in clinical trials uses patient characteristics to increase the likelihood of detecting a drug effect, reducing variability and de-risking outcomes.
Prognostic and predictive enrichment approaches are used, with predictive enrichment common in oncology and increasingly in other diseases.
Trial design and enrichment directly influence drug labeling, affecting physician prescribing, insurance coverage, and commercial market size.
Most recent FDA-approved cancer drugs used predictive biomarkers for enrichment, a trend expanding to other therapeutic areas.
Measurement and gaps in atopic dermatitis trials
Disease severity in atopic dermatitis is measured by vIGA (lesion severity) and EASI (extent of disease), both critical for patient assessment.
Current systemic therapies require an EASI ≥16, excluding patients with severe but localized disease from access to these drugs.
This measurement gap leaves patients with high severity but low extent (low EASI) with unmet medical needs, as they are ineligible for systemic treatments.
Enriching trials to include both localized and extensive moderate-to-severe cases could address this gap and better reflect clinical reality.
Adaptive trial design and interim findings
The trial uses a two-stage adaptive design, with the first 50 patients unblinded for interim analysis to refine endpoints and enrichment criteria.
Self-reported pruritus (itch) score emerged as a key enrichment factor, with higher scores correlating with greater treatment effect separation.
Statistical significance was achieved in week 4 vIGA and EASI-75 endpoints, with dramatic separation at higher pruritus thresholds.
Stage 2 of the trial uses a baseline pruritus score ≥7 and stratifies patients by EASI to ensure balanced representation across disease extent.
Interim data showed compelling efficacy, with significant improvements in vIGA and EASI-100 at week 8, supporting the trial's enrichment strategy.
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