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NASDAQ:NEUP

Neuphoria Therapeutics Q4 2026 Earnings Report

Neuphoria Therapeutics logo
$3.70 -0.01 (-0.27%)
Closing price 09/18/2026 04:00 PM Eastern
Extended Trading
$3.74 +0.04 (+1.08%)
As of 09/18/2026 07:30 PM Eastern
Extended trading is trading that happens on electronic markets outside of regular trading hours. This is a fair market value extended hours price provided by Massive. Learn more.

Neuphoria Therapeutics EPS Results

Actual EPS
N/A
Consensus EPS
-$1.58
Beat/Miss
N/A
One Year Ago EPS
N/A

Neuphoria Therapeutics Revenue Results

Actual Revenue
N/A
Expected Revenue
N/A
Beat/Miss
N/A
YoY Revenue Growth
N/A

Neuphoria Therapeutics Announcement Details

Quarter
Q4 2026
Time
After Market Closes
Conference Call Date
Friday, September 18, 2026
Conference Call Time
7:00AM ET

Earnings Documents

Neuphoria Therapeutics Earnings Headlines

Reviewing Moderna (NASDAQ:MRNA) and Neuphoria Therapeutics (NASDAQ:NEUP)
Neuphoria Therapeutics Inc Ordinary Shares NEUP
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Neuphoria Therapeutics Inc (NEUP)
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About Neuphoria Therapeutics

Neuphoria Therapeutics (NASDAQ:NEUP), Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for obesity and other metabolic diseases. The company’s research programs are designed to address conditions involving weight management, diabetes and metabolic dysfunction.

Neuphoria’s pipeline includes DA-1726, an investigational dual GLP-1 and glucagon receptor agonist being developed for obesity and related metabolic conditions. The company is also developing DA-1241, an investigational GPR119 agonist intended for metabolic dysfunction-associated steatohepatitis, formerly known as nonalcoholic steatohepatitis, and other metabolic disorders. These programs originated through collaborations and licensing arrangements with Dong-A-related entities.

The company was formerly known as NeuroBo Pharmaceuticals, Inc. and adopted the Neuphoria Therapeutics name as its business focus evolved toward metabolic disease therapies. As a clinical-stage company, Neuphoria does not yet have an established portfolio of commercially marketed products. Its programs remain subject to clinical development, regulatory review and potential approval.

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