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Enanta Pharmaceuticals to Present Data for Zelicapavir, an Oral, Once-Daily, N-Protein Inhibitor, in Development for the Treatment of Respiratory Syncytial Virus, at IDWeek™ 2026

Key Takeaway: Enanta Pharmaceuticals announced that it will present data on zelicapavir, an oral N-protein inhibitor for respiratory syncytial virus (RSV), at IDWeek 2026. The presentation will detail results from a Phase 2 trial demonstrating the drug's effectiveness in reducing symptom resolution time and hospitalization in high-risk adults. The event will take place from October 21-24, 2026, in Washington, DC.

Market Sentiment Analysis

POSITIVE FACTORS

  • Enanta Pharmaceuticals is advancing its innovative treatment for RSV.
  • Zelicapavir shows promise in reducing hospitalization and viral load.
  • Presentation at IDWeek 2026 highlights significant clinical trial results.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+19%
120-day peak, hindsight
Typical move
19.8%
average across 3 past catalysts
Cash runway
~62 mo
Minimal dilution risk
Lead asset
EDP-235
Phase 2 · COVID-19

Full Press Release Details

Enanta Pharmaceuticals to Present Data for Zelicapavir, an Oral, Once-Daily, N-Protein Inhibitor, in Development for the Treatment of Respiratory Syncytial Virus, at IDWeek™ 2026

WATERTOWN, Mass.--(BUSINESS WIRE)--Oct. 13, 2026-- Enanta Pharmaceuticals, Inc. (NASDAQ:ENTA), a clinical stage biotechnology company dedicated to creating novel, small molecule drugs for viral infections and immunological diseases, today announced that data for zelicapavir, its oral, once-daily, N-protein inhibitor in development for the treatment of respiratory syncytial virus (RSV), will be presented at IDWeek™ 2026 being held October 21-24, 2026 virtually and at the Walter E. Washington Convention Center in Washington, DC.
Details of the presentation are as follows:
Poster Title: Zelicapavir Decreases Time to Complete RSV Symptom Resolution, Hospitalization and Viral Load in a Global, Randomized, Double-Blinded, Placebo (PBO)-Controlled Phase 2 Trial of High-Risk Adults Poster Session: Novel Agents Poster Number: 3 Date: Thursday October 22, 2026 Time: 12:15 PM - 1:30 PM ET Location: Poster Hall B-C Presenter: Christopher E. Harris, M.D.
The poster will be available to view on the conference platform during the conference and on the Company’s website here. Further information about IDWeek™ 2026 can be found here.
About Enanta Pharmaceuticals, Inc. Enanta is using its robust, chemistry-driven approach and drug discovery capabilities to become a leader in the discovery and development of small molecule drugs for viral infections and immunological diseases. In virology, Enanta’s clinical programs are focused on the development of first-in-disease and best-in-disease treatments for respiratory syncytial virus (RSV). The Company’s immunology pipeline aims to develop treatments for inflammatory diseases by targeting key drivers of the type 2 immune response, with KIT, STAT6 and MRGPRX2 inhibition.
Glecaprevir, a protease inhibitor discovered by Enanta, is part of the only treatment approved for curing both acute and chronic hepatitis C virus (HCV) infection and is sold by AbbVie in numerous countries under the tradenames MAVYRET® (U.S.) and MAVIRET® (ex-U.S.) (glecaprevir/pibrentasvir). A portion of Enanta’s royalties from HCV products developed under its collaboration with AbbVie contribute ongoing funding to Enanta’s operations. Please visit www.enanta.com for more information.
View source version on businesswire.com: https://www.businesswire.com/news/home/20261013575271/en/

Media and Investors Contact Jennifer Viera 617-744-3848 jviera@enanta.com

Source: Enanta Pharmaceuticals, Inc.
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Frequently Asked Questions

What is Zelicapavir?

Zelicapavir is an oral, once-daily N-protein inhibitor developed for treating respiratory syncytial virus (RSV).

When will the data for Zelicapavir be presented?

The data will be presented at IDWeek 2026, from October 21-24, 2026.

What are the results of the Phase 2 trial for Zelicapavir?

The trial showed that Zelicapavir decreases time to symptom resolution, hospitalization, and viral load in high-risk adults.

Who is presenting the data on Zelicapavir?

Dr. Christopher E. Harris will present the data at IDWeek 2026.

Where can I find more information about the presentation?

Further details will be available on the conference platform and Enanta's website.

Last updated: Oct 13, 2026