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VBI Vaccines Inc/BC (VBIV)·Q2 2023 Earnings Summary
Executive Summary
- Q2 2023 was a transition quarter with tightened cost structure, a redefined U.S. field force, and added liquidity from a July public offering and expanded Brii partnership; reported net revenue rose to $0.72M, +108% YoY, driven by U.S. PreHevbrio and initial EU sales via Valneva .
- Non-GAAP net loss (ex-FX and impairment) improved to $18.7M from $23.8M YoY; GAAP net loss was $44.6M, reflecting a $20.0M impairment and $5.9M FX loss .
- Commercial momentum: average order size among switching accounts increased 46% QoQ; PreHevbrio global net product sales grew 48% QoQ to $0.7M; CDC adult vaccine contract award up to $25.4M supports public health channel push .
- Estimates context: S&P Global consensus was unavailable; a third-party source indicates Q2 EPS was -$2.17 vs a -$2.16 estimate (minor miss), revenue consensus not available .
- Near-term catalysts: APAC licensing with Brii (July) including $15M upfront and potential milestones and double-digit royalties, continued EU launches in H2 2023, and expected Canada availability in H1 2024 .
What Went Well and What Went Wrong
What Went Well
- PreHevbrio global net product sales increased 48% QoQ to $0.7M; momentum supported by targeted U.S. commercial redeployment completed in June .
- “Q2 was a period of transition…we believe we are well-positioned going into the second half of 2023 to execute on our corporate strategy and drive growth and value” – Jeff Baxter, CEO .
- Strategic deals: expanded APAC licensing with Brii ($15M upfront, $3M equity, up to $422M milestones, double-digit royalties); CDC adult vaccine contract award up to $25.4M .
What Went Wrong
- GAAP net loss remained elevated at $44.6M due to a $20.0M impairment and $5.9M FX loss, despite lower SG&A; FX volatility linked to intercompany loans and currency translation .
- Cost of revenues increased with scaling production, keeping gross profit constrained relative to net sales growth .
- Cash declined to $20.8M at quarter-end (pre-July financing/partnership proceeds), underscoring liquidity needs amid pipeline execution .
Financial Results
Segment/KPI detail:
Margins (Gross Profit Margin %, EBITDA Margin %, EBIT Margin %) were not disclosed in the press releases, and S&P Global fundamentals were unavailable for VBIV mapping during retrieval.
Guidance Changes
Earnings Call Themes & Trends
No Q2 2023 earnings call transcript was found; VBIV did not provide an earnings call transcript in our document catalog or investor site for Q2 2023. Special call transcript exists for Feb 28, 2023 but is not Q2 earnings-related ; Q2 2023 press release used for themes.
Management Commentary
- “Q2 was a period of transition…we believe we are well-positioned going into the second half of 2023 to execute on our corporate strategy and drive growth and value” – Jeff Baxter, President & CEO .
- “We continue to focus on three core priorities: (1) making a difference in the fight against hepatitis B, (2) advancing key development programs, and (3) managing our operational expenses and capital to fuel sustainable growth” – Jeff Baxter (Q1 remarks) .
- On HBV therapeutic strategy: initial Phase 2 data “underscore the belief that a functional cure…is within reach, and that our immunotherapeutic candidate, VBI-2601, has the potential to be a meaningful part of that combination regimen” .
Q&A Highlights
No Q2 2023 earnings call transcript was available; thus no Q&A highlights or clarifications can be provided from a call. Themes and specific quotes are drawn from press releases and SEC 8-K filings .
Estimates Context
- S&P Global consensus estimates for Q2 2023 were unavailable due to missing mapping for VBIV in the retrieval system.
- A third-party source indicates Q2 2023 EPS actual -$2.17 vs estimate -$2.16 (minor miss). Revenue consensus not available from that source .
- Given the GAAP impairment charge ($20.0M) and FX loss ($5.9M), non-GAAP results better reflect core operations; non-GAAP net loss improved to $18.7M YoY, which may inform future estimate revisions focused on operating loss trajectory .
Key Takeaways for Investors
- Commercial execution is improving: targeted U.S. redeployment and EU launches drove higher PreHevbrio utilization and average order size; expect continued uptake in H2 2023 and into Canada in H1 2024 .
- Cash at quarter-end was $20.8M, but July financing ($20.5M gross) and Brii upfront ($15M incl. $3M equity) materially strengthened liquidity; watch cash runway versus pipeline timelines .
- Non-GAAP losses narrowed YoY even as GAAP was impacted by non-recurring impairment and FX; track OpEx discipline (30-35% reduction targeted for H2 vs H2 2022) and FX exposure from intercompany loans .
- CDC contract award up to $25.4M is a notable public health channel catalyst; monitor execution and purchase pacing across immunization programs .
- Strategic alignment around HBV (PreHevbrio prevention, VBI-2601 therapeutic) plus APAC licensing leverages partner commercialization and potential milestones/royalties; focuses capital on highest-return opportunities .
- Near-term pipeline readouts (VBI-1901 GBM Phase 2b initiation/dosing; VBI-2901 Phase 1 interim) could add optionality; investor focus remains on commercial HBV traction and operating efficiency .
- With S&P consensus unavailable and limited external estimates, price-driving narrative hinges on visible revenue growth, OpEx execution, and partnership milestones rather than quarterly EPS optics .
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