Companies
Cybin, now Helus Pharma
Summary
Cybin, now Helus Pharma, is a biopharmaceutical company developing deuterated serotonergic compounds, with HLP003/CYB003 in Phase 3 and a sudden April 2026 CEO reversal now part of the company’s live record.
Why it matters
Cybin’s shift into Helus Pharma is a continuity problem and a governance problem at the same time: the name changed, the lead program kept moving, and the board still removed a freshly installed CEO after only 69 days without giving investors a substantive public explanation.
Research notes
Context, reporting, and structured background for this dossier.
Cybin said in January 2025 that it would rebrand as Helus Pharma and shift its U.S. listing to Nasdaq. That means the company’s official public identity changed, but the older Cybin name still matters for continuity across reporting, stock-market references, and trial-program history.
That continuity problem got sharper in April 2026. Helus had only just installed Michael Cola as chief executive in February, then said on April 20 that Cola was stepping down effective immediately at the request of the board and that co-founder and executive chairman Eric So would again serve as interim CEO. The company kept investor attention on Phase 3 continuity, but the public explanation for the reversal stayed notably thin.
Continuity and naming
The rebrand is not just cosmetic. It changes the official site, investor-relations surface, and how newer program materials are titled. This page keeps the legacy cybin route while making the current Helus identity explicit, so readers can connect the older company record to the current one without breaking continuity.
Clinical program
Helus’s own program materials now describe HLP003, formerly referred to as CYB003, as a deuterated novel serotonergic agonist with FDA Breakthrough Therapy Designation for adjunctive treatment of major depressive disorder. The company’s clinical-trials page explicitly notes that HLP003 was formerly CYB003, which helps close the naming gap between older Cybin-era reporting and newer Helus-era program language.
The Phase 3 PARADIGM program, outlined in Helus investor materials, organizes the depression effort into APPROACH, EMBRACE, and EXTEND. Public registry coverage through NCT06564818 helps anchor the program in a checkable trial record rather than only investor copy.
Leadership whiplash in April 2026
The more structurally important update is the leadership break. Helus introduced Michael Cola on February 10 as the operator who would lead the company’s next phase of scale, execution, and commercialization planning. Sixty-nine days later, the company said Cola was leaving at the board’s request and that Eric So would resume the interim chief executive role while the search restarted.
That does not automatically change the Phase 3 program. It does change how the company should be read. A board-requested CEO removal that fast, with no substantive public explanation, becomes part of the company record whether or not the trial calendar stays intact.
Why this page matters
Cybin/Helus remains one of the more advanced psychedelic-compound developers and one of the clearest examples of how naming continuity, investor communications, clinical-trial status, and governance can drift apart if the dossier is not maintained carefully. The route stays cybin, but the live company, program language, and management story now belong to Helus.
Citations and source links
Source material used to ground or extend this dossier.
- [10] NCT06564818
Related reporting
Recent SCM reporting that overlaps this dossier’s company, program, or governance record.
- Helus Pharma Replaced Michael Cola After Just 69 Days as CEO
Helus says Michael Cola stepped down at the board's request and Eric So is back as interim CEO. The sharper fact is timing: the company hired Cola on Feb. 10 and removed him 69 days later without a public explanation.
- Trial Tracker: What's Moving in Early 2026
Cybin's CYB003 program is recruiting in phase 3, Mount Sinai is running an MDMA therapist-training study, Brigham has a severe alcohol use disorder protocol queued up, and smaller psilocybin studies in OCD and antidepressant interaction remain active.
- FDA Offers Faster Review Pathway for Three Psychedelic Drug Programs
FDA says three psychedelic drug programs are getting access to the CNPV accelerated-review pathway. COMPASS has directly confirmed one award; Usona and Transcend/Otsuka have not.
Related entities
Other dossiers that help connect this page to the wider reporting record.
- Psilocybin
- Treatment-Resistant Depression (TRD)
- FDA
The U.S. Food and Drug Administration is the gatekeeper for psychedelic drug development in the United States, from IND clearance through advisory committee review and any eventual approval or rejection.