According to Ethris, ETH47 reduced viral load 40-fold at day 2, the time of peak replication.1 Peak LRSS was 14% lower and LRSS area under the curve (AUC) was 58% lower with ETH47 vs placebo.1
Episodes meeting a mild exacerbation definition, an LRSS rise of at least 2 points, were 30% lower when sustained over 2 consecutive days and 56% lower over 3 days.1 Jackson Cold Score AUC was 53% lower, and the proportion of participants developing a cold was 37% lower.1
ETH47 safety and exploratory IFNλ exposure-response findings
Ethris reported no severe or serious adverse events (AEs), no systemic exposure, and no anti-DMG-PEG antibodies after the single nasal dose.1 Local IFNλ expression was detected in nearly all dosed participants at 6 hours.1
Key Facts
What is ETH47?
ETH47 is an investigational nasally administered mRNA therapy from Ethris designed to induce local IFNλ expression in the airway to strengthen innate antiviral defense in patients with asthma.
Did ETH47 meet its primary endpoint?
Ethris reported a consistent numerical trend toward improvement in lower respiratory symptom score, the primary endpoint, but did not report statistical significance for this or any other outcome.
What did the ETH47 phase 2a trial show?
In 50 adults with asthma challenged with rhinovirus A16, a single ETH47 dose reduced peak viral load 40-fold and lowered LRSS AUC by 58% vs placebo, with no serious adverse events.
Challenge-related respiratory treatment-emergent AEs were 73% lower and rescue medication use was 65% lower with ETH47.1 Spirometry showed numerical improvements, according to the company.1
In an exploratory exposure-response analysis, effects were greater in participants with higher IFNλ exposure, including a more than 100-fold viral load reduction on days 2 and 3, a 19-fold lower peak viral load, and a 46% lower peak LRSS.1 The release did not state how many participants were in this subgroup or how higher exposure was defined.
"The clear relationship between exposure and effect will inform dose and regimen optimization in the next study," said Carsten Rudolph, PhD, cofounder and chief executive officer, Ethris.1
Ethris plans a multiple-ascending-dose phase 1 study in patients with asthma and chronic obstructive pulmonary disease (COPD), a phase 2a rhinovirus challenge study in COPD, and phase 2b field studies in both populations.1 The company is also developing a spray-dried dry powder formulation designed for room-temperature stability.1
References
Ethris. Ethris reports positive topline phase 2a data for nasal mRNA candidate ETH47 in asthma patients challenged with rhinovirus. Published November 5, 2026. Accessed November 5, 2026. https://www.globenewswire.com/news-release/2026/11/05/3396091/0/en/ethris-reports-positive-topline-phase-2a-data-for-nasal-mrna-candidate-eth47-in-asthma-patients-challenged-with-rhinovirus.html
Ethris. Ethris presents positive topline phase 1 data with mRNA lead candidate ETH47 for uncontrolled asthma. Published January 30, 2025. Accessed November 5, 2026. https://www.businesswire.com/news/home/20250130943965/en/Ethris-Presents-Positive-Topline-Phase-1-Data-with-mRNA-Lead-Candidate-ETH47-for-Uncontrolled-Asthma