Recent 8-K filings for TTRX
Highest-materiality recent filing
Turn Therapeutics Announces Final Stage 2 Design and Expansion of GX-03 Phase 2 Trial
- Interim analysis of GX-03 Phase 2 trial in atopic dermatitis showed Week 4 vIGA-AD Success 71.4% vs 33.3% vehicle in EASI 1.1-7.0 subgroup.
- Final Stage 2 design will enroll 120-135 patients across full EASI spectrum (≥1.1) using Hochberg multiple testing procedure for four endpoints.
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Turn Therapeutics Announces Final Stage 2 Design and Expansion of GX-03 Phase 2 Trial
Interim analysis of GX-03 Phase 2 trial in atopic dermatitis showed Week 4 vIGA-AD Success 71.4% vs 33.3% vehicle in EASI 1.1-7.0 subgroup.
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Turn Therapeutics GX-03 Phase 2 interim: 92.6% EASI-50 at 4 weeks; no SAEs
92.6% of GX-03 subjects achieved EASI-50 at 4 weeks vs 65.2% vehicle; 70.4% achieved EASI-75.
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Turn Therapeutics appoints former FDA Commissioner Dr. Stephen Hahn as clinical and regulatory lead
Dr. Stephen M. Hahn, former FDA Commissioner, appointed to oversee clinical and regulatory strategy for GX-03.
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Turn Therapeutics reports FY2025 net loss of $3.2M; secures up to $25M venture debt
Cash and equivalents $5.08M as of Dec 31, 2025, excludes $7M initial tranche from Avenue Capital facility.
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Turn Therapeutics secures up to $25M growth capital loan from Avenue Capital Group
Initial $7M tranche funded at closing; up to $18M additional available upon clinical and corporate milestones.
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Phase 2 trial of GX-03 for moderate-severe atopic dermatitis on track; interim and topline data expected first half of 2026.
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Turn Therapeutics Q3 net loss $1.9M; enters global Medline PermaFusion deal
Net loss of $1.9M ($0.07/share) vs $0.67M loss in Q3 2024; G&A surged to $1.75M on listing costs.
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Turn Therapeutics enters global supply, development, and license agreement with Medline
Agreement covers development, manufacture, and commercialization of products using Turn's PermaFusion delivery platform.
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Turn Therapeutics enters global supply and development pact with Medline for PermaFusion platform
Turn grants Medline exclusive worldwide license to use Turn's 510(k) clearance for wound-care field-of-use.
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Phase 2 trial of GX-03 (topical IL-36/IL-31 inhibitor) for moderate-severe eczema: ~25% of targeted sample completed, no safety concerns; topline results expected in 2026.
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Turn Therapeutics effects direct listing on Nasdaq; appoints two independent directors
SEC declared effective S-1 for direct listing of up to 17,868,760 shares of common stock on Nasdaq Global Market.
Earnings & guidance
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