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Journal of Clinical Medicine· 2026Q2

Clinical Outcomes in Placebo-Injection and Injection-Free Cohorts in Birch Pollen Allergy: An Exploratory Cross-Study Comparison

Esther Raskopf, Carmen Fierro Ballester, Hacer Sahin, Nadine Katzke et al.

Short summary

Placebo injections in birch pollen allergy trials led to descriptively lower symptom and medication scores (37-50% reduction) compared to an injection-free placebo cohort.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Placebo-injection cohorts in birch pollen allergy trials showed descriptively lower median CSMS (1.34 and 1.07) compared to an injection-free cohort (2.14).
  • The observed reductions in CSMS for placebo-injection cohorts were approximately 37% and 50% lower than the injection-free cohort.
  • Similar patterns of lower symptom and medication scores were seen in placebo-injection cohorts for daily symptom scores (0.78/0.70 vs 1.22) and daily medication scores (0.39/0.36 vs 0.93).
  • The study compared data from three separate prospective clinical trials, assembling placebo-injection cohorts from two and an injection-free cohort from one.

AI-generated from the title and abstract; the full text is not read.

Abstract

Background/Objectives: Placebo responses can complicate the interpretation of allergen immunotherapy (AIT) trials because symptom- and medication-based outcomes may be influenced by the trial context in addition to treatment-specific effects. Injection-free comparison cohorts are rarely available in conventional double-blind, placebo-controlled AIT trials. We therefore conducted an exploratory post hoc cross-study comparison of clinical outcomes in two placebo-injection cohorts and an injection-free cohort of birch pollen-allergic participants. Methods: Data from three prospective clinical studies evaluating the mannan-conjugated birch pollen allergoid EP-088-T502—T502-SIT-020, T502-SIT-045, and T502-SIT-068—were assembled for this cross-study comparison. Placebo-injection cohorts from studies T502-SIT-020 and T502-SIT-045 were compared with the injection-free cohort from study T502-SIT-068. Clinical outcomes included the Combined Symptom and Medication Score (CSMS), daily Symptom Score (dSS), and daily Medication Score (dMS). Results: The primary peak-period analysis included 60, 93, and 160 participants from T502-SIT-020, T502-SIT-045, and T502-SIT-068, respectively. During the site-specific 14-day peak birch pollen periods, median CSMS was 2.14 in the injection-free cohort compared with 1.34 and 1.07 in the T502-SIT-020 and T502-SIT-045 placebo-injection cohorts, respectively. These values corresponded descriptively to approximately 37% and 50% lower cohort medians, respectively, relative to the injection-free cohort. Median dSS, which was defined consistently across the three source studies, was 1.22 in the injection-free cohort compared with 0.78 and 0.70 in the two placebo-injection cohorts. Median dMS was 0.93 compared with 0.39 and 0.36, respectively. The same between-cohort pattern was observed in the secondary fixed 1–30 April analysis. Conclusions: Both placebo-injection cohorts showed lower CSMS and dSS values than the injection-free cohort. Because the cohorts were non-concurrent and derived from separate studies, the observed differences do not establish a causal effect of placebo injections.

The authors' abstract, as published at the source. Journal of Clinical Medicine, 2026 · DOI ↗

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Field: Immunology and Allergy

Immunology and AllergyMedicine