Tonix Receives FDA Clearance for Phase 2 Trial of TNX-102 SL for Major Depressive Disorder.
ByAinvest
Wednesday, Dec 3, 2025 10:16 am ET1min read
TNXP--
Tonix Pharmaceuticals Holdings has received FDA clearance to launch a Phase 2 trial for its drug TNX-102 SL to treat major depressive disorder (MDD) in adults. The trial, called HORIZON, will enroll 360 adults across 30 US clinical sites and compare TNX-102 SL against placebo. Tonix aims to advance TNX-102 SL as a novel therapeutic option for the substantial unmet medical need in MDD, which affects over 21 million adults in the US annually.

Stay ahead of the market.
Get curated U.S. market news, insights and key dates delivered to your inbox.
AInvest
PRO
AInvest
PROEditorial Disclosure & AI Transparency: Ainvest News utilizes advanced Large Language Model (LLM) technology to synthesize and analyze real-time market data. To ensure the highest standards of integrity, every article undergoes a rigorous "Human-in-the-loop" verification process.
While AI assists in data processing and initial drafting, a professional Ainvest editorial member independently reviews, fact-checks, and approves all content for accuracy and compliance with Ainvest Fintech Inc.’s editorial standards. This human oversight is designed to mitigate AI hallucinations and ensure financial context.
Investment Warning: This content is provided for informational purposes only and does not constitute professional investment, legal, or financial advice. Markets involve inherent risks. Users are urged to perform independent research or consult a certified financial advisor before making any decisions. Ainvest Fintech Inc. disclaims all liability for actions taken based on this information. Found an error?Report an Issue

Comments
No comments yet