
Nuance Biotech is a biopharma company spanning respiratory, emergency care, iron deficiency anemia, and pain management.
nuancepharma.comCrawled Nov 8, 2026
Emergency Care
The page describes iron deficiency anemia.
Nuance Pharma are an innovation focused biopharmaceutical company, with both late-stage clinical pipeline and commercial stage asset portfolio across respiratory, emergency care, iron deficiency anemia and pain management.
Nuance Pharma begins dosing the first patient in its **REACH Phase III trial** of **STG320 (Actair®)**, a treatment for **house dust mite-induced allergic rhinitis**, in China. The trial marks a key milestone for the biopharmaceutical company’s development of the therapy. STG320 targets allergic rhinitis, a condition affecting millions globally. Nuance Pharma’s Phase III study aims to further validate the drug’s safety and efficacy in a broader patient population.
Oct 2026PR NewswireNews article
Nuance Pharma secures **IND clearance** from China’s NMPA for its **Actair®** pivotal clinical trial, advancing house dust mite allergy immunotherapy for Chinese patients. The approval marks a critical milestone in the drug’s regulatory pathway, enabling patient enrollment in China. Actair® targets a common respiratory allergy affecting millions globally.
May 2026PR NewswireNews article
Nuance Pharma publishes Phase 3 trial results showing Ohtuvayre® (ensifentrine) improves lung function in Chinese adult patients. The data appears in the peer-reviewed *CHEST* journal, validating the drug’s efficacy in a clinical setting. The study, named ENHANCE-CHINA, contributes to the growing body of evidence for ensifentrine’s respiratory benefits.
Apr 2026PR NewswireNews article
Nuance Pharma secures regulatory approval for **Ohtuvayre® (ensifentrine)**, a COPD treatment, in **Hong Kong SAR, China**. This marks its second approval outside the U.S., expanding patient access in select **Special Administrative Regions (SARs)** of Greater China. The drug targets chronic obstructive pulmonary disease (COPD) and follows prior U.S. FDA clearance.
Mar 2026PR NewswireNews article