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Cybin Acquires Dmt Clinical Study From Entheon Biomedical

PUBLIC · HELPJun 07, 2022

Acquiring Company

Helus Pharma

Acquired Company

the CYB004-E Study

TorontoOtherManufacturingBiotechnologyHealth CarePharmaceuticalOtherConsumer GoodsScience And EngineeringGovernment And Military

Description

Cybin Inc. (NEO:CYBN) (NYSE American:CYBN) (Cybin or the Company), a biopharmaceutical company focused on progressing “Psychedelics to TherapeuticsTM”, today announced that, through its wholly-owned subsidiary Cybin IRL Limited, it has entered into an agreement to acquire a Phase 1 N,N-dimethyltryptamine (“DMT”) study (the “Acquisition”) from Entheon Biomedical Corp. (CSE: ENBI) (OTCQB: ENTBF) (FSE: 1XU1) (“Entheon”) to accelerate the clinical development path for CYB004, Cybin’s proprietary deuterated DMT molecule for the potential treatment of anxiety disorders.

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Company Information

Company

Helus Pharma

Location

Toronto, Ontario, Canada

About

Helus Pharma is a mental health-focused biopharmaceutical company developing small-molecule Novel Serotonergic Agonists (NSAs) to improve treatment options. The company is advancing patient-centered innovation through clinical excellence to deliver meaningful and durable outcomes that support long-term healing.

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Frequently asked

Who acquired the CYB004-E Study?

the CYB004-E Study was acquired by Helus Pharma, based in Toronto. The deal was reported on June 7, 2022. Helus Pharma is a mental health-focused biopharmaceutical company developing small-molecule Novel Serotonergic Agonists (NSAs) to improve treatment options. Helus Pharma is publicly traded (HELP) and operates in Other.

When did Helus Pharma acquire the CYB004-E Study?

Helus Pharma's acquisition of the CYB004-E Study was reported on June 7, 2022. Cybin Inc. Fundz records the date the transaction was first publicly reported, sourced from filings and company announcements.

What does the CYB004-E Study do?

The CYB004-E study is an adaptive, randomized, double-blind, placebo-controlled, single ascending dose study to evaluate the safety, pharmacokinetics (“PK”) and pharmacodynamics (“PD”) of a target-controlled intravenous infusion of DMT in healthy smokers. It is privately held, operating in Other.

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