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BioWorld - Thursday, February 12, 2026
Home » Topics » Disease categories and therapies » Respiratory

Respiratory
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Phase IIb study of nebulized ensifentrine meets primary endpoints

Jan. 16, 2020

Novel TMEM16A potentiator shows promise in models of CF

Jan. 16, 2020
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In with the new

Boehringer inks $1B+ antifibrosis deal with Singapore's Enleofen Bio

Jan. 14, 2020
By Michael Fitzhugh
Fresh off ending one antifibrosis program in December, Boehringer Ingelheim GmbH (BI) is spinning up an expansive new effort in the area this month, promising Singapore-based Enleofen Bio Pte. Ltd. potential payouts of more than $1 billion per product from a preclinical interleukin-11 platform.
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Verona climbs on solid phase IIb data for COPD therapy; phase III to start this year

Jan. 13, 2020
By Nuala Moran
LONDON – Verona Pharma plc reported positive phase IIb results for the nebulized formulation of its dual phosphodiesterase (PDE) 3 and 4 inhibitor, ensifentrine (RPL-554), as an add-on to standard bronchodilation therapy in chronic obstructive pulmonary disorder (COPD).
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Inhalation specialist CF Pharmtech closes $90M series E

Jan. 10, 2020
By Elise Mak
BEIJING – CF Pharmtech Inc., of Suzhou, China, closed a ¥630 million (US$90 million) series E financing round to bring its inhaled respiratory drugs to global markets and replace imports with homegrown products faster.
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Redx Pharma nominates ROCK2 inhibitor RXC-007 as drug development candidate in fibrosis

Jan. 10, 2020
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In with the new

Boehringer inks $1B+ antifibrosis deal with Singapore's Enleofen Bio

Jan. 9, 2020
By Michael Fitzhugh
Fresh off ending one antifibrosis program in December, Boehringer Ingelheim GmbH (BI) is spinning up an expansive new effort in the area this month, promising Singapore-based Enleofen Bio Pte. Ltd. potential payouts of more than $1 billion per product from a preclinical interleukin-11 platform.
Read More

Atyr’s potential $175M deal with Kyorin bILD-ing the case for lead sarcoidosis candidate

Jan. 7, 2020
By Randy Osborne
San Diego-based Atyr Pharma Inc. CEO Sanjay Shukla told BioWorld that the company plans to move into a registrational trial with lead candidate ATYR-1923 in pulmonary sarcoidosis (PS) if data from the ongoing phase Ib/IIa trial, due later this year, turn out positive. Releasing patients from steroid burdens “would be a real game-changer,” he said, noting that people with PS take as much as 25 mg of prednisone per day to control their coughs and shortness of breath. 
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Atyr’s potential $175M deal with Kyorin bILD-ing the case for lead sarcoidosis candidate

Jan. 6, 2020
By Randy Osborne
San Diego-based Atyr Pharma Inc. CEO Sanjay Shukla told BioWorld that the company plans to move into a registrational trial with lead candidate ATYR-1923 in pulmonary sarcoidosis (PS) if data from the ongoing phase Ib/IIa trial, due later this year, turn out positive. Releasing patients from steroid burdens “would be a real game-changer,” he said, noting that people with PS take as much as 25 mg of prednisone per day to control their coughs and shortness of breath. 
Read More

Chiesi Farmaceutici identifies ROCK1 and ROCK2 inhibitors

Jan. 3, 2020
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