OI
OmniAb, Inc. (OABI)·Q2 2024 Earnings Summary
Executive Summary
- Q2 revenue was $7.61M (+9.6% y/y; +100% q/q), driven by a one-time $1.3M acceleration of deferred service revenue from GSK’s ion channel program discontinuation; net loss improved to $13.63M and EPS to -$0.13 from -$0.19 in Q1. Management reiterated 2H weighting of milestones.
- Guidance tightened: total operating expenses now expected to be slightly less than 2023 (previously “approximately the same”), cash use similar to 2023 (ex-TECVAYLI milestone), and substantially lower in 2025 on milestone cadence leverage.
- Business momentum: 83 active partners (+3 q/q), 333 active programs (+6 q/q), 32 clinical/commercial programs; new licenses with DAAN Bio, Topaz Therapeutics, 92Bio, and MSKCC; continued expansion of OmnidAb and xPloration AI-enabled screening platform.
- Stock reaction catalysts: near-term partner readouts and starts (e.g., acasunlimab Phase 3 initiation in 2024; sugemalimab EU approval progressing to commercialization partnerships; Teva’s TEV-56278 entered clinic), plus expected 2H milestone weighting and 2025 cash burn inflection.
What Went Well and What Went Wrong
What Went Well
- Added multiple new partners (DAAN Bio, Topaz Therapeutics; recently 92Bio and MSKCC) and grew partners/programs net of attrition; “this year has the potential to be our best year ever in new partners and licenses.”
- Technology leadership reinforced: OmnidAb peer-reviewed publication and xPloration platform progress with AI/deep learning integration; new patents on microcapillary array screening.
- Financial discipline: G&A down y/y on lower SBC and non-recurring ERP costs; operating expenses now expected slightly below 2023; cash of $57.2M at quarter-end supports runway.
What Went Wrong
- Revenue mix lifted by non-recurring service revenue acceleration ($1.3M) due to GSK discontinuation; underlying milestone revenue remained 2H-weighted.
- Asset attrition: GSK discontinued small molecule Nav1.1; Roche returned Kv7.2 rights post-quarter—OmniAb will seek repartnering but near-term revenue impact limited.
- YTD revenue down sharply versus 2023 due to prior-year milestone timing (TECVAYLI EU $10M in 2023), highlighting dependence on partner milestones for growth.
Financial Results
P&L vs Prior Periods and y/y
Notes:
- Q2 revenue increase due to $1.3M accelerated service revenue from GSK program termination; milestone revenue remains 2H-weighted per management.
- Net margin improvement q/q reflects higher revenue and other operating income from CVR liability reduction ($2.6M) and non-cash impairment effects (amortization up due to $1.2M).
Revenue Mix
KPIs
Balance Sheet Snapshot: Cash, cash equivalents & ST investments were $57.2M at 6/30/24; $69.0M at 3/31/24; $87.0M at 12/31/23.
Guidance Changes
Drivers: Lower opex reflects SBC and ERP non-recurring costs abating, and tighter expense control; 2025 cash use drop expected from increased milestone inflows as programs advance stages.
Earnings Call Themes & Trends
Management Commentary
- “Given the velocity of new deals and a growing book of business, this year has the potential to be our best year ever in new partners and licenses.” — CEO Matt Foehr
- “This revenue was consistent with our expectations with the exception of higher service revenue… [GSK program] triggered an acceleration of $1.3 million in service revenue.” — CFO Kurt Gustafson
- “Operating expenses… now expect total operating expenses in 2024 to be slightly less than total operating expenses in 2023.” — CFO
- “xPloration… can be paired with deep learning and AI… to really increase throughput.” — CEO
Q&A Highlights
- Exploration platform strategy: optionality to provide instruments to partners in future; IP characterized as microcapillary-based, unique, and AI-integrated.
- Milestone visibility: forecasts based on mix of public and partner information; more program visibility as assets enter the clinic.
- Asset returns & repartnering: CNS small molecule assets from GSK/Roche at discovery/preclinical stages; co-ownership enables repartnering opportunities.
- 2025 revenue/cash dynamics: primary driver expected to be milestone revenue; royalties currently modest, potential incremental EU royalties from sugemalimab.
Estimates Context
- S&P Global consensus estimates for Q2 2024 revenue and EPS were unavailable for OABI due to missing CIQ mapping in the SPGI dataset; therefore, beat/miss assessment versus Street cannot be determined this quarter. [SpgiEstimatesError: Missing CIQ mapping for ticker 'OABI']
Where estimates may need to adjust:
- 2H milestone weighting reiterated and new clinical starts increase the probability of milestone timing into late 2024/2025; revenue phasing expectations should reflect the one-time $1.3M service revenue uplift in Q2 and potential incremental sugemalimab royalties in EU subject to commercial partner execution.
Key Takeaways for Investors
- Revenue quality: headline Q2 growth benefited from a non-recurring $1.3M service revenue acceleration; focus on 2H milestone cadence for sustainable growth.
- Expense discipline: opex guide tightened lower vs 2023; expect operating leverage as partner/program count grows without material opex increases.
- Pipeline catalysts: watch acasunlimab Phase 3 initiation in 2024, Immunovant batoclimab/IMVT-1402 data timeline, and additional OmniAb-derived entries into the clinic (target 4–6 in 2024).
- Royalties optionality: sugemalimab EU approval with a 3% royalty rate could add royalties as commercialization partners are secured; timing remains uncertain.
- Repartnering potential: returned CNS ion channel assets present optional licensing opportunities; near-term revenue impact likely limited but supports optionality.
- Cash trajectory: expect substantially lower cash use in 2025 driven by milestone inflows; current cash of $57.2M supports runway.
- Trading setup: narrative hinges on execution of partner catalysts and visibility into milestones in 2H; technology differentiation (OmnidAb, xPloration+AI) and partner growth support medium-term multiple expansion if milestones convert.
Appendix: Additional Data and Disclosures
- Other operating income in Q2 includes a $2.6M reduction in contingent liabilities (CVRs) primarily due to GSK/Roche program changes; amortization increased due to a $1.2M impairment tied to legacy Ab Initio programs.
- Royalty detail: sugemalimab carries a 3% royalty on worldwide sales; EU commercialization partner pending.
Note: Consensus estimates (S&P Global) were unavailable for OABI this quarter; beat/miss vs Street cannot be assessed.