AstraZeneca reports positive Phase III trial results for COPD drug
Get Alerts AZN Hot Sheet
Join SI Premium – FREE
AstraZeneca PLC (NASDAQ: AZN) reported that its experimental drug tozorakimab met the primary endpoint in a Phase III trial for chronic obstructive pulmonary disease patients.
The MIRANDA trial showed tozorakimab demonstrated a statistically significant reduction in the annualized rate of moderate-to-severe COPD exacerbations compared to placebo. The results applied to both the primary population of former smokers and the overall population that included current and former smokers.
Patients in the trial received tozorakimab 300mg or placebo every two weeks in addition to standard care. The study enrolled COPD patients who continued experiencing moderate-to-severe exacerbations while on inhaled standard treatments.
"These results add to the growing body of evidence that indicates tozorakimab delivered meaningful clinical benefits for COPD patients who urgently need new treatment options," said Frank Sciurba, a professor at the University of Pittsburgh and chief investigator of the LUNA program.
The company previously announced positive results from two other Phase III trials, OBERON and TITANIA, testing tozorakimab at a four-week dosing interval in March.
Tozorakimab is described as a potential first-in-class monoclonal antibody targeting interleukin-33. The drug was generally well tolerated with a safety profile consistent with previous trials, according to the company.
AstraZeneca plans to submit the data to regulatory authorities and present findings at an upcoming medical meeting. The company also is studying tozorakimab in Phase III trials for severe viral lower respiratory tract disease and Phase II trials for asthma.
COPD affects nearly 400 million people globally and ranks as the third leading cause of death worldwide. More than 50% of patients experience exacerbations despite standard inhaled treatments.
Serious News for Serious Traders! Try StreetInsider.com Premium Free!
You May Also Be Interested In
- TRUQAP® (capivasertib) combination approved in the US as first and only targeted treatment for PTEN-deficient metastatic hormone-sensitive prostate cancer
- TechCreate Group faces NYSE American delisting proceedings
- Circle board member resigns after nearly 13 years of service
Create E-mail Alert Related Categories
Corporate News, FDA, Hot Corp. NewsRelated Entities
Maynard Um, Mark Zuckerberg, ARKSign up for StreetInsider Free!
Receive full access to all new and archived articles, unlimited portfolio tracking, e-mail alerts, custom newswires and RSS feeds - and more!



Tweet
Share