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Galectin Therapeutics has received written feedback from the FDA on its Belapectin program for MASH cirrhosis and portal hypertension. The FDA has aligned with Galectin on the patient population for a registration trial and plans to extend a follow-up Type C meeting to finalize trial design elements and present new biomarker data. Galectin has also secured a $10 million credit line to fund expenditures through at least March 2027.

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