Laurent Pharma Gets US FDA Approval To Begin Phase 2 RESOLUTION Study To Treat COVID-19

Laurent Pharma Gets US FDA Approval To Begin Phase 2 RESOLUTION Study To Treat COVID-19

Laurent Pharmaceuticals, a Montreal-based biopharmaceutical company, announced that it has received approval from the Food and Drug Administration (FDA) to start enrolling US patients in RESOLUTION; a multicentric phase 2 randomized placebo-controlled trial testing once-a-day oral LAU-7b as a potential treatment against COVID-19 disease. RESOLUTION, which is currently ongoing in Canada, will enroll approximately 200 hospitalized COVID-19 patients who will receive either LAU-7B or a placebo for treatment duration of 14 days. The company is in advanced discussions with a number of US hospitals interested to participate in the trial and is looking to activate them very soon.“The main objective of the RESOLUTION study is to demonstrate that LAU-7b is a safe and effective treatment option for COVID-19 patients that are at risk of lung complications because of their age, underlying condition or both,” said Dr. Radu Pislariu MD, president and CEO of Laurent Pharmaceuticals. “We hope that treatment with LAU-7b will slow down the disease progression, prevent the respiratory failure requiring mechanical ventilation, and ultimately reduce the number of fatalities due to the COVID-19,” added Dr. Pislariu.LAU-7b, which showed potent antiviral effects in-vitro against both SARS-CoV-2 and MERS-CoV coronaviruses, is also being developed for its unique inflammation-controlling properties by acting on the resolution phase of the inflammation process, a natural mechanism that keeps the body's inflammatory response under control without inducing immune-suppression (a pro-resolving effect). The pro-resolving proprieties of LAU-7b are currently under evaluation in a phase 2 study in Cystic Fibrosis (CF), aiming to treat the exaggerated inflammatory response that leads to irreversible lung damage in these patients.“New clinical research approaches for COVID-19 aim to combine antiviral with inflammation-controlling treatments,” said Dr. Dana G. Kissner, MD, pulmonologist at DMC Harper University Hospital and Professor of Medicine, Wayne State University, in Detroit, Michigan. “During the less critical stages of the disease, we want therapies that fight the virus while keeping the inflammation in check and preventing lung complications. LAU-7b appears to possess both properties in the same molecule, thus bearing the promise of a treatment candidate that addresses multiple key contributors to the severity of COVID-19,” added Dr. Kissner.

Optimize Your trial insights with Clival Database.

Are you exhausted from the uncertainty of trial insights pricing? Clival Database ensures the clarity in the midst of the global scenario for clinical trials to you.

Clival Database is one of the best databases that offers an outstanding number of clinical trial data in terms of 50,000+ molecules and from primary regulatory markets as well as new entrants like Indian and Chinese markets.

With Clival, you get accurate positioning of historical sales data, patent database, company profiling, safety & efficacy, and prediction of launch of new innovative molecules helping you to align your research and driving down the cost.

To add value, we further break down our analytics for you so that improving your operational effectiveness; optimizing your clinical trials; and offering you accurate and high-quality data at lowest possible prices becomes possible.

Elevate your trial success rate with the cutting-edge insights from Clival database.

Check it out today and make more informed sourcing decisions! Learn More!