NeuroBo Pharmaceuticals Receives First Site IRB Approval For Its Phase 1 Clinical Trial Evaluating DA-1726 For Treatment Of Obesity
Portfolio Pulse from Benzinga Newsdesk
NeuroBo Pharmaceuticals has received the first site Institutional Review Board (IRB) approval for its Phase 1 clinical trial of DA-1726, a drug aimed at treating obesity. This marks a significant step forward in the development of DA-1726 and highlights NeuroBo's commitment to addressing obesity through innovative treatments.
February 29, 2024 | 1:06 pm
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NeuroBo Pharmaceuticals has received IRB approval for the Phase 1 trial of its obesity treatment, DA-1726, indicating progress in its development pipeline.
The IRB approval for the Phase 1 trial of DA-1726 is a critical regulatory milestone that typically leads to positive investor sentiment, as it demonstrates progress in the drug's development. This approval is likely to be viewed positively by the market, potentially leading to an increase in NRBO's stock price in the short term.
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