Anebulo Pharmaceuticals Initiates Phase 1 Clinical Trial of IV Selonabant for Acute Cannabis-Induced Toxicity in Children

Reuters
09/25
Anebulo Pharmaceuticals Initiates Phase 1 Clinical Trial of IV Selonabant for Acute Cannabis-Induced Toxicity in Children

Anebulo Pharmaceuticals Inc. has announced the dosing of the first subjects in its Phase 1 single ascending dose (SAD) study of intravenous (IV) selonabant, a drug under development for the treatment of acute cannabis-induced toxicity. The study is being conducted in healthy young adults and is supported by a collaborative grant from the National Institute on Drug Abuse (NIDA). Selonabant was previously evaluated as an oral treatment in a Phase 2 clinical trial, with the company now prioritizing the IV formulation for potential use in pediatric patients. According to Anebulo, interactions with the U.S. Food and Drug Administration (FDA) are ongoing, with a focus on developing selonabant for children exposed to cannabis toxicity. No efficacy or safety results from the current Phase 1 study have been presented yet; further updates are expected as the study progresses.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Anebulo Pharmaceuticals Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20250925857310) on September 25, 2025, and is solely responsible for the information contained therein.

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