FDA
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SELLAS Life Sciences Reports Second Quarter 2025 Financial Results and Provides Corporate Update
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SELLAS Announces Positive Overall Survival in Cohort 3 from the Ongoing Phase 2 Trial of SLS009 in r/r AML
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SELLAS Life Sciences Reports Second Quarter 2024 Financial Results and Provides Corporate Update
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SELLAS Life Sciences (SLS) Granted FDA Rare Pediatric Disease Designation for SLS009
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GenFleet and BeiGene Enter into Trial Collaboration for a Potentially First-in-class Combination Therapy to Initiate Phase Ib/II Study of GFH009 (CDK9 inhibitor) and BRUKINSA® (zanubrutinib) Treating
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SELLAS Receives FDA Orphan Drug Designation for SLS009 for Treatment of Peripheral T-cell Lymphomas
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SELLAS Life Sciences (SLS) Receives Fast Track Designation from FDA for SLS009 for Treatment of Relapsed/Refractory Peripheral T-cell Lymphomas
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