Sign in

You're signed outSign in or to get full access.

AB

ARTELO BIOSCIENCES, INC. (ARTL)·Q2 2019 Earnings Summary

Executive Summary

  • No revenue and a net loss of $344,883 in the quarter ended May 31, 2019, a YoY improvement driven by a $563,966 non-cash gain from revaluing derivative liabilities; operating expenses rose to $941,288, reflecting higher G&A and professional fees .
  • The company strengthened liquidity post-quarter via an $8.0M gross public offering and uplisted to Nasdaq; management cites $7.3M net proceeds as a key catalyst enabling the ART27.13 license exercise and near-term trial initiation plans .
  • Pipeline progressed: ART27.13 expected to enter a Phase 1b/2a study for cancer-related anorexia toward end-2019; ART12.11 CBD cocrystal process chemistry expected to be finalized “over the next few months”; ART26.12 investigational application studies planned for Q4 2019 .
  • No Wall Street consensus estimates were available via S&P Global for this micro-cap, pre-revenue biotech; comparisons vs estimates are not applicable.

What Went Well and What Went Wrong

  • What Went Well

    • Liquidity improvement and market visibility: Completed $8.0M gross public offering and uplisted to Nasdaq; management highlighted $7.3M net proceeds and stronger financial position to execute programs .
    • Pipeline momentum: “We have focused on placing Artelo in a stronger financial position… This financing enabled us to exercise our option to in-license ART27.13, our lead development candidate that is expected to enter a Phase 1b/2a study… toward the end of 2019.” — Gregory D. Gorgas, CEO .
    • Non-cash gain reduced quarterly loss: Change in fair value of derivative liabilities produced a $563,966 gain, lowering net loss to $344,883 versus $577,857 in the prior-year quarter .
  • What Went Wrong

    • No revenue: Company reiterated it has not generated revenues since inception; operating cash burn persisted (nine-month operating cash outflow of $1,731,580) .
    • Higher operating costs: Operating expenses increased to $941,288 from $577,857 YoY on G&A and professional fees; research and development was $184,204 vs $236,845 in the prior year quarter .
    • Going concern and controls: Substantial doubt about ability to continue as a going concern; disclosure controls and procedures were not effective as of the quarter end .

Financial Results

MetricQ2 2018 (3 mo ended May 31, 2018)Q1 2019 (3 mo ended Feb 28, 2019)Q2 2019 (3 mo ended May 31, 2019)
Revenue ($USD)$0 $0 $0
Operating Expenses ($USD)$577,857 $757,919 $941,288
Net Loss ($USD)$(577,857) $(424,789) $(344,883)
Basic EPS ($USD)$(0.36) $(0.03) $(0.17)
Diluted EPS ($USD)$(0.36) $(0.05) $(0.40)
Change in Fair Value of Derivative Liabilities ($USD)$0 $(333,130) (expense) $563,966 (gain)

Note: The company effected a 1-for-8 reverse split on June 20, 2019; Q2 2019 per-share amounts are retroactively adjusted in that filing, while Q1 2019 reflects pre-split reporting, limiting direct EPS comparability .

KPIs and Operating Detail

KPIQ2 2018Q1 2019Q2 2019
Research & Development ($USD)$236,845 $489,981 $184,204
General & Administrative ($USD)$104,564 $57,922 $402,803
Professional Fees ($USD)$236,375 $209,946 $354,038
Cash & Cash Equivalents (period end, $USD)N/A$457,328 $286,439

Segment breakdown: Not applicable (no revenue) .

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
ART27.13 Phase 1b/2a start (cancer-related anorexia)CY2019 (late)“Planning to initiate… late 2019” “Expected to enter… toward the end of 2019” Maintained
ART12.11 CBD cocrystal process chemistryNext few months (CY2019)Not specified previously“Expect to… finalize the process chemistry over the next few months” New specific timing
ART26.12 investigational application studiesQ4 2019“Initiate IND enabling… anticipate clinical studies in cancer can begin in 2020” “Plan to initiate investigational application studies in the fourth quarter of 2019” Accelerated near-term step
Financial guidance (Revenue, margins, OpEx)FY2019None providedNone providedMaintained (no financial guidance)

Earnings Call Themes & Trends

TopicPrevious Mentions (Q1 2019)Current Period (Q2 2019)Trend
Capital markets & listingPre-Nasdaq; highlighted need to raise capital; working capital deficiency $8.0M gross offering; uplisted to Nasdaq; $7.3M net proceeds Improving liquidity & visibility
ART27.13 programPlanning Phase 1b/2a in late 2019 License exercised; trial “toward the end of 2019” Execution progress
ART12.11 CBD cocrystalIP filed in late 2018; program rationale described “Finalize process chemistry over the next few months” Near-term manufacturing readiness
ART26.12 FABP5 inhibitorLate pre-clinical; IND-enabling forthcoming; clinical in 2020 “Initiate investigational application studies in Q4 2019” Advancing toward regulatory step
Controls & going concernSubstantial doubt; controls not effective Substantial doubt; controls not effective Unchanged risk posture

Note: No earnings call transcript was furnished; the company provided an Item 2.02 press release as the primary earnings communication .

Management Commentary

  • “The first half of 2019 has been a period of transformation for Artelo… raised a total of $8.9 million to date in 2019, including our recently completed financing of $7.3 million in net proceeds with a concurrent up listing to the Nasdaq. This financing enabled us to exercise our option to in-license ART27.13… expected to enter a Phase 1b/2a study… toward the end of 2019.” — Gregory D. Gorgas, President & CEO .
  • “With ART12.11… we expect to be able finalize the process chemistry over the next few months, which is an important step leading to GMP manufacturing.” — Gregory D. Gorgas .
  • “We believe our FABP5 program… holds significant potential… we plan to initiate investigational application studies in the fourth quarter of 2019.” — Gregory D. Gorgas .

Q&A Highlights

  • Not applicable; no earnings call transcript was located in the company’s filings for the period, with the earnings communication furnished via press release under Item 2.02 .

Estimates Context

  • S&P Global/Capital IQ consensus estimates for revenue and EPS for the quarter ended May 31, 2019 were unavailable; as a pre-revenue micro-cap biotech, the company’s results are not compared to Wall Street consensus in this recap.

Key Takeaways for Investors

  • Liquidity and listing upgrade materially de-risk near-term execution: $8.0M gross offering and Nasdaq uplisting improve access to capital and investor visibility; management cited $7.3M net proceeds enabling pipeline milestones .
  • Near-term clinical catalyst: ART27.13 Phase 1b/2a initiation for cancer-related anorexia by end-2019 is a potential stock-moving event as dosing/weight gain endpoints are evaluated .
  • Manufacturing readiness for CBD cocrystal: ART12.11 process chemistry finalization in coming months supports GMP ramp and future IND/clinical steps .
  • FABP5 program advancing: Initiation of investigational application studies in Q4 2019 could clarify regulatory path ahead of anticipated 2020 oncology clinical work .
  • Operating discipline vs burn: Nine-month operating cash outflow of $1.73M underscores the importance of recent financing; cash was $286,439 at quarter-end before the offering .
  • Accounting/controls and going concern remain watchpoints: Substantial doubt and ineffective disclosure controls persist; monitor remediation steps post-uplisting .
  • Derivative liability dynamics can swing reported net loss: The $563,966 gain this quarter reduced loss; future revaluations may introduce non-cash volatility .

Supporting documents:

  • Q2 2019 10-Q for the period ended May 31, 2019 .
  • Item 2.02 8-K with earnings press release (Third Quarter 2019 financial results and corporate update) .
  • 8-Ks on offering, reverse split, and uplisting with related press releases .