Benzinga | Dec 22, 2021 07:10AM EST

UAB And Mereo Announce Top-Line Results From COSTA Phase 1b/2 Trial Of Alvelestat (MPH966) In Hospitalized Patients With COVID-19 Respiratory Disease; Says 'Alvelestat reported safe and well-tolerated in patients with COVID-19'

Alvelestat reported safe and well-tolerated in patients with COVID-19

Alvelestat, on top of standard of care resulted in a more rapid time to improvement in WHO Disease Severity score of >=2 in the first 5-7 days compared to placebo plus standard of care



LONDON and REDWOOD CITY, Calif., Dec. 22, 2021 (GLOBE NEWSWIRE) -- The University of Alabama at Birmingham (UAB) and Mereo BioPharma Group plc (NASDAQ:MREO), today announced top-line data from a Phase 1b/2 clinical trial evaluating alvelestat, a novel, orally active Neutrophil Elastase (NE) inhibitor in hospitalized COVID-19 Respiratory Disease patients.

The COSTA Phase 1b/2 trial (NCT04539795) is an investigator-led, single-centre study (Principal Investigator Dr. James M Wells, Associate Professor in Pulmonary, Allergy and Critical Care Medicine, UAB). The trial is a double-blind, randomized, placebo-controlled study in adult patients (>18 years) with COVID-19 Respiratory Disease, evaluating the safety and tolerability of alvelestat on top of Standard of Care in patients hospitalised with proven COVID-19 lung disease. Patients requiring mechanical ventilation were excluded. Enrolled subjects received alvelestat or matched placebo, twice daily, for 5 days, with optional extension to 10 days per investigator judgement. Initial subjects underwent dose escalation to evaluate safety and tolerability for the population. The Primary Endpoint was Safety and Tolerability to Day 60, with mortality assessment at Day 90. Secondary Endpoints were clinical outcomes to Day 60. Biomarkers of inflammation, coagulopathy, were measured; biomarkers of neutrophil extracellular traps (NETs) were explored and desmosine was measured to the end of study drug treatment. The study was signal seeking and not powered for the secondary measures.

Fifteen patients were randomized (10 male, 5 female), and all completed the Primary Endpoint Safety assessment to Day 60 and the Day 90 final study assessment. The original design involved a 2:1 active to placebo ratio, however patients were enrolled 1:1 resulting in 8 patients on alvelestat and 7 patients on placebo. The mean age was 47.8 years; the most common co-morbidities were hypertension, sleep apnea, hypercholesterolemia, and Type 2 diabetes. At entry to the study, all patients were requiring supplemental oxygen, all had initiated dexamethasone and 14 were on antiviral treatment with remdesivir at baseline or initiated after randomization (7/7 on placebo and 7/8 on alvelestat). The majority of patients were WHO COVID-19 Ordinal Severity Scale Score 4 (hospitalized mild disease requiring supplemental oxygen) or 5 (hospitalized severe disease, requiring non-invasive ventilation or high flow oxygen) at entry to the study.

TRIAL RESULTS HIGHLIGHTS

Primary Endpoint: Safety and Tolerability to Day 60

* Consistent with the known safety profile of alvelestat, no safety signals were observed in lab safety monitoring, including none in liver, renal and vital sign parameters.

* Treatment emergent headaches were more frequent in the alvelestat arm (4/8 - all of moderate severity) compared to placebo (1/8 of mild severity). Three patients in the alvelestat arm were noted to also have headache in the screening period. None were considered study-drug related by the investigator. There was no difference in frequency of other adverse events between alvelestat and placebo arms to Day 60.

* A single SAE of hospital readmission for acute hypoxemic respiratory failure COVID-19 was reported in the alvelestat arm and was not considered drug related by the investigator.

* There were no deaths on study (to end of study assessment at Day 90).

Secondary Efficacy Endpoints:

Clinical Outcome Measures

* In the alvelestat arm 62.5% (5/8) patients had a 2-point decrease in the WHO Disease Severity score by Day 5, compared to 28.5% (2/7) patients in the placebo arm. At Day 7 this improvement in WHO Severity score increased to 87.5% (7/8) in the alvelestat arm and 57% (4/7) in the placebo arm.

Inflammatory Biomarkers

* The pro-inflammatory blood biomarker, Interleukin-6 was elevated in this population and decreased in the alvelestat arm from baseline at end of treatment compared to an increase from baseline for placebo (p=0.193). Consistent with this response, a greater reduction in C-reactive Protein was observed in alvelestat compared to placebo (p=0.143) In addition, there was a reduction in D-Dimer in the alvelestat arm in comparison to the placebo arm which increased over the treatment period (p=0.199). These biomarkers support an early-onset of effect of alvelestat on the inflammatory and pro-coagulopathy pathways. The majority of the other inflammatory biomarkers were not elevated at baseline, as expected for patients treated with dexamethasone and consequently no clear changes with treatment could be observed. TNF-alpha which was elevated at baseline, showed a reduction in both alvelestat and placebo arms (p value NS).

Other Biomarkers

* Desmosine was not elevated in the majority of patients at baseline in the alvelestat arm and consequently no treatment effect could be detected.

* Detailed analysis of blood biomarkers of NETosis, generally within the normal range at baseline, is ongoing.

"There remains a significant unmet need to improve the outcomes of hospitalized patients with COVID-19. The early results with alvelestat suggest a potential for clinical benefit over and above standard of care including dexamethasone and remdesivir. This is exciting given the ease of administration of a well-tolerated oral therapy in this acutely ill population," said Dr. Mike Wells, Associate Professor in Pulmonary, Allergy and Critical Care Medicine, UAB. "These findings provide strong data and set the stage for future studies with relevant clinical end-points."

"These data whilst early and in a small study, are highly encouraging as the first evidence that alvelestat could offer clinical outcome benefit over and above standard of care in patients hospitalized with COVID-19," said Dr. Denise Scots-Knight, Chief Executive Officer at Mereo. "This clearly warrants further evaluation in a larger study. We are grateful to the patients who participated in this study and to Dr. Mike Wells and his team at UAB for leading this important work."