The US Food and Drug Administration (FDA) has  approval for Azurity ÎÛÎÛÂþ®‹s’ Konvomep (omeprazole and sodium bicarbonate for oral suspension) to treat active benign gastric .
Konvomep is also indicated for lowering the upper gastrointestinal bleeding risk in critically ill patients.
It is a combination of a proton pump inhibitor (PPI), omeprazole, and sodium bicarbonate.
The company plans to make Konvomep available commercially in pharmacies across the country in the first quarter of next year.
Azurity ÎÛÎÛÂþ®‹s CEO Richard Blackburn said: “We are very pleased that patients will soon have access to this FDA-approved oral liquid formulation option of a commonly prescribed proton pump inhibitor.
“Patients are our priority, and our purpose is to bring them new formulations that help them benefit from established medicines.
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By GlobalData“Konvomep may give patients, particularly patients with difficulty swallowing pills or capsules, an option for treatment tailored to their needs.â€
A pharmaceutical firm, Azurity focuses on developing new products for the special requirements of overlooked patients.
Currently, the company has products across the cardiovascular, endocrinology, neurology, gastro-intestinal, institutional and orphan markets.
In July, the FDA granted approval for Azurity’s Zonisade (zonisamide oral suspension) 100mg/5mL as an adjunctive treatment for partial seizures in adults as well as paediatric epilepsy patients aged 16 years and above.
Given once or twice a day, Zonisade is said to be the first zonisamide formulation for oral liquid dosing to receive FDA approval in this indication.
Zonisamide’s efficacy and tolerability were validated in three placebo-controlled, double-blind, multicentre trials.
To date, the safety of efficacy of the therapy is not validated in people aged below 16 years.