{"id":17546,"date":"2023-04-07T02:00:00","date_gmt":"2023-04-07T02:00:00","guid":{"rendered":"https:\/\/www.prnasia.com\/story\/archive\/4063728_CN63728_0"},"modified":"2023-04-07T02:00:00","modified_gmt":"2023-04-07T02:00:00","slug":"nuance-pharma-announces-dosing-of-first-patient-in-enhance-china-phase-iii-trial-for-chronic-obstructive-pulmonary-disease-copd","status":"publish","type":"post","link":"https:\/\/transmediavictoria.net.au\/?p=17546","title":{"rendered":"Nuance Pharma Announces Dosing of First Patient in ENHANCE – China Phase III Trial for Chronic Obstructive Pulmonary Disease (“COPD”)"},"content":{"rendered":"

SHANGHAI<\/span>, April 7, 2023 \/PRNewswire\/ — Nuance Pharma (“the Company”) announces dosing of first patient in the ENHANCE – China Phase III Trial for the maintenance treatment of chronic obstructive pulmonary disease (“COPD”) of its novel solution Ensifentrine in mainland China<\/span>.<\/span><\/p>\n

Ensifentrine is a first-in-class, selective, dual inhibitor of the enzymes phosphodiesterase 3 and 4 (“PDE3” and “PDE4”) combining bronchodilator and non-steroidal anti-inflammatory activities in one compound. This activity has the potential to alleviate respiratory symptoms such as breathlessness and cough, as well as providing anti-inflammatory benefits for those with COPD.<\/p>\n

Ensifentrine Study in China<\/span><\/i><\/b><\/p>\n

On August 17<\/span>th<\/sup>, 2022, Nuance Pharma announced the IND approval from the Center for Drug Evaluation (CDE) for supporting its pivotal Phase I and Phase III clinical trials of Ensifentrine in the maintenance treatment of COPD.<\/p>\n

March 9<\/span>th<\/sup>, 2023, Nuance Pharma completed first dosing of the first healthy subject in the Phase I trial (RPL554 – AHC001; NCT05758428), a PK, safety and tolerability study of nebulized Ensifentrine on healthy Chinese volunteers.<\/p>\n

April 6<\/span>th<\/sup>, 2023, Nuance Pharma announces the first COPD patient dosed in the ENHANCE – CHINA<\/span> Phase III trial (RPL554 – CPC001; NCT05743075), a randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and safety of Ensifentrine over 24 weeks in patients with moderate to severe COPD.<\/p>\n

“It gives me great pleasure to announce the first dosing of ENHANCE-China Phase III trial. This represents a crucial milestone for our collaboration with Verona Pharma and is indicative of a strong opening to the China<\/span> clinical development program. Ensifentrine combines bronchodilator and non-steroidal anti-inflammatory properties in one compound, differentiating it from existing drug classes used to treat COPD” commented Mark G. Lotter<\/span>, CEO and Co-Founder of Nuance Pharma. “We are looking forward to introducing this novel drug in Greater China<\/span> to address unmet needs in the COPD market.”<\/p>\n

“We are pleased our development partner, Nuance Pharma, has begun pivotal studies in COPD with ensifentrine in mainland China<\/span>,” said David Zaccardelli<\/span>, Pharm. D., President and Chief Executive Officer of Verona Pharma. “This is a significant milestone and, based on our recent highly positive Phase III results in COPD, we are excited about the potential of ensifentrine to address the urgent global need for a novel treatment for COPD.”<\/p>\n

December 20<\/span>th<\/sup>, 2022, Nuance’s global partner Verona Pharma announced Ensifentrine met primary and key secondary endpoints in Phase III ENHANCE-1 trial for COPD, after positive readout for Phase III ENHANCE-2 trial for COPD in August 2022<\/span>, another step closer to providing a much-needed novel therapy for COPD patients. Verona Pharma plans to submit a New Drug Application to the US Food and Drug Administration in the second quarter of 2023.<\/p>\n

About Ensifentrine<\/b><\/p>\n

Ensifentrine (RPL554) is an investigational, first-in-class, selective dual inhibitor of the enzymes phosphodiesterase 3 and 4 that combines bronchodilator and anti-inflammatory activities in one compound. In Phase II clinical studies in COPD, ensifentrine has shown significant and clinically meaningful improvements in lung function, symptoms and quality of life as a monotherapy or added onto a maintenance bronchodilator. In the Phase III ENHANCE-1 and ENHANCE-2 clinical trials, ensifentrine showed significant and clinically meaningful improvements in lung function measures and reduced the rate of COPD exacerbations. Ensifentrine has been well tolerated in clinical trials involving approximately 3,000 subjects to date.<\/p>\n

About Nuance Pharma<\/b><\/p>\n

Nuance Pharma is an innovation focused biopharmaceutical company, with both late-stage clinical pipeline and commercial stage asset portfolio. Focusing on specialty care, Nuance has established a differentiated combination of commercialized assets and innovative pipeline across respiratory, pain management, emergency care and iron deficiency anemia.<\/p>\n

With the mission to address critical unmet medical needs in Asia Pacific, Nuance deploys the Dual Wheel model that develops a global leading innovative pipeline, while maintaining a self-sustainable commercial operation in both China and Asia as a region. For more information, please visit www.nuancepharma.com<\/a>.<\/p>\n

About Verona Pharma<\/b><\/p>\n

Verona Pharma is a clinical-stage biopharmaceutical company focused on developing and commercializing innovative therapies for the treatment of respiratory diseases with significant unmet medical needs. If successfully developed and approved, Verona Pharma’s product candidate, ensifentrine, has the potential to be the first therapy for the treatment of respiratory diseases that combines bronchodilator and anti-inflammatory activities in one compound. The Company has evaluated nebulized ensifentrine in its Phase III clinical program ENHANCE (“Ensifentrine as a Novel inHAled Nebulized COPD thErapy”) for COPD maintenance treatment. Ensifentrine met the primary endpoint in both ENHANCE-1 and ENHANCE-2 trials demonstrating statistically significant and clinically meaningful improvements in lung function. In addition, ensifentrine significantly reduced the rate and risk of COPD exacerbations in ENHANCE-1 and ENHANCE-2. Two additional formulations of ensifentrine are in Phase II development for the treatment of COPD: dry powder inhaler and pressurized metered-dose inhaler. Ensifentrine also has potential applications in cystic fibrosis, asthma and other respiratory diseases. For more information, please visit www.veronapharma.com<\/a>.<\/p>\n

Forward-Looking Statement:<\/b><\/p>\n

This announcement includes forward-looking statements that involve risks, uncertainties and other factors, many of which are outside of our control, that could cause actual results to differ materially from the results discussed in the forward-looking statements. Forward-looking statements include statements concerning our plans, objectives, goals, future events, performance and\/or other information that is not historical information. All such forward-looking statements are expressly qualified by these cautionary statements and any other cautionary statements which may accompany the forward-looking statements. We undertake no obligation to publicly update or revise forward-looking statements to reflect subsequent events or circumstances after the date made, except as required by law. <\/p>\n

Company contacts:<\/b><\/p>\n

Nuance Pharma<\/b><\/p>\n

Vicky Lin<\/span>, IR & PR Senior Manager, Email: vicky.lin@nuancepharma.cn<\/a><\/p>\n

Verona Pharma<\/b><\/p>\n

Victoria Stewart<\/span>, Senior Director of Investor Relations and Communications, Email: Victoria.Stewart@veronapharma.com<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

SHANGHAI, April 7, 2023 \/PRNewswire\/ — Nuance Pharma (“the Company”) announces dosing of first patient in the ENHANCE – China Phase III Trial for the maintenance treatment of chronic obstructive pulmonary disease (“COPD”) of its novel solution Ensifentrine in mainland China. 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