Enanta’s Path Forward Uncertain After RSV Failure

Despite High-Risk Studies To Come

The US biotech’s RSV treatment candidate has failed a Phase II study in low-risk patients leaving some experts skeptical of its hopes for potential improved performance in a high-risk setting.  

RSV Is A Major Cause Of Respiratory Illness Among Young Children • Source: Shutterstock

Enanta Pharmaceuticals, Inc.’s EDP-938 has failed a mid-stage trial in respiratory syncytial virus (RSV) and while the firm was upbeat about a path forward in high-risk patients, some experts remain unconvinced.

EDP-938 missed several endpoints in the Phase IIb RSVP study but Enanta plans to continue development of the drug in a different subset of RSV patients. The placebo-controlled trial studied 66 people aged 18 to 75 years with confirmed RSV infection within 48 hours of symptom onset

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