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NeuroBo Pharmaceuticals Receives Safety Review Committee Approval to Continue With Its Phase 2a Clinical Trial Evaluating DA-1241 for the Treatment of MASH

Blinded Safety Review Completed for the First 6 Months of the Phase 2a Clinical Trial Conduct; Recommending Trial Continue Without Modification Full Data Readout Expected in the Second Half of.

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Cambridgeshire
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Neurobo-pharmaceuticals-inc
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Neurobo-pharmaceuticals

NeuroBo Pharma Gets Approval To Proceed With Phase 2a Trial For DA-1241 To Treat MASH; Stock Up 8%

Biotechnology company NeuroBo Pharmaceuticals, Inc. (NRBO) announced Wednesday the receipt of Safety Review Committee (SRC) approval, recommending that the two-part Phase 2a trial of DA-1241 can continue without modification following a blinded safety review of the first six months of study conduct.

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NeuroBo Receives First Site IRB Approval For DA-1726 Obesity Trial; Stock Gains

Biotechnology company NeuroBo Pharmaceuticals, Inc. (NRBO), Thursday announced that it has received first site Institutional Review Board or IRB approval for Alexander Prezioso, Investigator, Clinical Pharmacology of Miami, to proceed with the Phase 1 clinical trial of DA-1726 for the treatment of obesity.

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Neurobo-pharmaceuticals-inc
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NeuroBo Pharmaceuticals (NRBO) Receives First Site IRB Approval for Its Phase 1 Trial of DA-1726

NeuroBo Pharmaceuticals (NRBO) Receives First Site IRB Approval for Its Phase 1 Trial of DA-1726
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Florida
United-states
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Institutional-review-board
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Icheon-kim
Chief-executive-officer
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