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Canadian psychedelic biotech developing conjugated psilocin formulations for treatment-resistant conditions. Spun out its proprietary Conjugated Psilocin™ technology to Cynaptec Pharmaceuticals in April 2025 via an $8.46 million financing round. Lead programme L-130 targets cluster headache disorder.

Development Programmes

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L-130 (Psilocin Mucate / Conjugated Psilocin™)

Psilocybin
Phase I

Chronic cluster headache / opioid use disorder

Programme Tracker

Headache Disorders (Cluster & Migraine)

Primary: US (FDA)
Phase IActive

Phase 1a complete (10 HVs, Jordan, NCT06035900); Pre-IND discussions with FDA underway; development via Cynaptec Pharmaceuticals subsidiary ($8.46M financing at $22.56M valuation)

Milestones

regulatory-designation

In progress

Pre-IND work advancing per FDA guidance; preparing for US clinical trial authorization

Why it matters: FDA Pre-IND marks the transition from international (Jordan Phase 1a) to US regulatory pathway. Success would enable Phase 1b/2 in the US for cluster headache.

Watch next: Pre-IND FDA feedback; US Phase 1b/2 trial design for cluster headache; OUD programme initiation

Trial start

Completed

Actual: Jun 27, 2023

Phase 1 clinical trial initiated in Jordan (NCT06035900): 10 healthy volunteers, open-label, single oral dose PK study of L-130 (Psilocin Mucate)

Why it matters: L-130 is a proprietary stabilized psilocin conjugate with superior bioavailability vs psilocybin (which requires hepatic conversion to psilocin). Direct psilocin delivery provides more predictable pharmacokinetics and potentially faster onset.

phase-1-results

Completed

Actual: Dec 7, 2023

Phase 1 completed: all subjects dosed with no significant adverse events; Cmax significantly higher than expected

Why it matters: Higher-than-expected peak plasma concentration validates L-130's superior bioavailability hypothesis. No safety signals. Data supports progression to efficacy studies.

Efficacy data

Completed

Actual: Jun 1, 2024

Phase 1 PK results published in Journal of Clinical Pharmacology and Therapeutics (peer-reviewed)

Why it matters: Peer-reviewed publication provides the definitive Phase 1a data record and supports the Pre-IND submission to FDA.

preclinical-data

Completed

Actual: Jan 1, 2025

Preclinical paper published in Journal of Psychoactive Drugs: daily administration of L-130 produces favorable safety profile and anxiolytic effects in rodents exposed to chronic stress

Why it matters: Demonstrates daily dosing safety and anxiolytic efficacy in a chronic stress model — relevant for cluster headache patients who experience chronic/episodic pain cycles. L-130 may work both acutely and prophylactically.

Funding milestone

Completed

Actual: Jun 1, 2025

Cynaptec Pharmaceuticals (64% owned by Lobe Sciences) completed $8.46M financing at $22.56M post-money valuation

Why it matters: Substantial capitalization for the subsidiary running L-130 development. Lobe retains majority control while de-risking via subsidiary structure. R&D spending increased 130x year-over-year, signaling real clinical advancement.

Company milestone

Completed

Actual: Sep 9, 2025

Presentation at Clusterbusters 20th Annual U.S. Patient Conference (Grapevine, TX)

Why it matters: Cluster headache patient community engagement. Clusterbusters is the leading cluster headache advocacy organization and the primary patient recruitment channel for cluster headache trials.

Recorded Events

Sep 9, 2025: Company milestone

Jun 1, 2025: Funding milestone

Jan 1, 2025: preclinical-data

Jun 1, 2024: Efficacy data

Dec 7, 2023: phase-1-results

Quick Facts

Type
Public Biotech
Ticker
CSE: LOBE
Lead Stage
Phase I
Website
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