Axcella long COVID treatment helps some patients in small trial
		
		 
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		 [August 02, 2022] 
		By Julie Steenhuysen 
		 
		CHICAGO (Reuters) - One of the first trials 
		aimed at tackling long COVID helped some patients recover from lingering 
		physical and mental fatigue, although the drug developed by Axcella 
		Health Inc failed on the small study's main goal of restoring the normal 
		function of mitochondria - the energy factories of cells. 
		 
		In the 41-patient pilot study released on Tuesday, for three of 21 
		patients who received the drug, AXA1125, their physical fatigue scores 
		returned to normal levels after 28 days of treatment, Axcella Chief 
		Medical Officer Margaret Koziel said in a phone interview. 
		 
		Others who received the drug also reported physical and mental 
		improvements that were deemed to be statistically significant as shown 
		on a scale developed to measure chronic fatigue, according to the 
		preliminary results, and the drug was shown to be safe and well 
		tolerated. 
		
		
		  
		
		"This trial is suggesting that a drug that's very safe to take and has 
		minimal side effects is causing substantial improvement in people's 
		physical and cognitive experience of fatigue," said Dr. Jason Maley, a 
		consultant for Axcella who runs a long COVID clinic at Beth Israel 
		Deaconess Medical Center in Boston. 
		 
		The drug, originally developed for fatty liver disease, aims to treat 
		the crushing chronic fatigue reported by more than half of long COVID 
		sufferers by restoring normal function of mitochondria, the minuscule 
		power plants that help cells perform properly. 
		
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			A patient suffering from Long COVID is examined by medical staff in 
			the post-coronavirus disease (COVID-19) clinic of Ichilov Hospital 
			in Tel Aviv, Israel, February 21, 2022. REUTERS/Amir Cohen 
            
			
			
			   
			People in the trial conducted at the University of Oxford received 
			either the Axcella drug or a placebo over a period of 28 days. All 
			were more than 12 weeks post COVID infection and had an abnormal 
			phosphocreatine recovery time, a measure of mitochondrial function. 
			For the study's primary goal, there was no 
			statistically significant difference between the groups on 
			phosphocreatine recovery time. 
			 
			The trial also looked at blood tests measuring lactate, a sign of 
			muscle health, as well as patient-reported measures of mental and 
			physical fatigue. 
			 
			There are currently no approved treatments for chronic fatigue in 
			patients with long COVID, a condition estimated to affect more than 
			one hundred million people worldwide. 
			 
			Axcella Chief Executive Bill Hinshaw said the company is designing 
			new trials and plans to meet with U.S. and UK regulators with hopes 
			of seeking an accelerated approval pathway for this enormous unmet 
			need. 
			 
			(Reporting by Julie Steenhuysen; Editing by Bill Berkrot) 
			
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