ZL
Zai Lab Ltd (ZLAB)·Q2 2025 Earnings Summary
Executive Summary
- Total revenues grew 9% year-over-year to $110.0M; product revenue rose 9% to $109.1M. Guidance was reaffirmed at $560–$590M for FY25, and management reiterated a path to adjusted profitability in Q4 2025 .
- Against S&P Global consensus, revenue missed ($125.0M estimate vs $110.0M actual), while EPS was better than expected (consensus -$0.415 vs actual -$0.37). Bolded below as significant miss/beat. Values retrieved from S&P Global.
- Commercial momentum was led by VYVGART, with record utilization and 46% q/q sales growth (to $26.5M), aided by updated national MG guidelines elevating use in both acute and maintenance settings .
- Key catalysts: positive Phase 3 bemarituzumab OS benefit (FORTITUDE-101) with China submission targeted 2H25; DLL3 ADC (ZL-1310) advancing to a registrational 2L ES-SCLC study; NMPA reviews/submissions for KarXT, TTFields, and efgartigimod PFS supporting 2H25–2026 launches .
What Went Well and What Went Wrong
What Went Well
- VYVGART delivered record patient utilization and 46% q/q sales growth to $26.5M, driven by longer treatment duration and growing maintenance adoption; July national MG guidelines further strengthen positioning for early and sustained treatment .
- Operating discipline: loss from operations improved 28% y/y to $(54.9)M; adjusted operating loss improved 37% y/y to $(34.2)M, keeping Q4 adjusted profitability on track .
- Pipeline execution: bemarituzumab plus chemo met OS at interim in FORTITUDE-101; ZL-1310 (DLL3 ADC) showed strong efficacy signals (67% ORR overall; 79% at 1.6 mg/kg) and FDA Fast Track, with pivotal 2L ES-SCLC initiation planned 2H25 .
- “We are making meaningful progress…With multiple launches ahead, a robust pipeline, and profitability within reach, Zai Lab is executing on its vision…” — Dr. Samantha Du .
- “With a 28% year-over-year reduction in operating loss…we are on track to achieve profitability in the fourth quarter.” — Josh Smiley .
What Went Wrong
- Revenue missed consensus in Q2; ZEJULA softened to $41.0M (vs $45.0M in Q2 2024) amid evolving PARPi competitive dynamics .
- XACDURO growth constrained by supply localization work; management flagged near-term 2025 growth limits despite strong underlying demand .
- Revenue growth was primarily product-driven but collaboration revenue remained modest ($0.9M), limiting diversification of topline .
Financial Results
Product gross metrics (calculated from cited figures):
Segment/product breakdown:
KPIs:
Guidance Changes
Earnings Call Themes & Trends
Management Commentary
- “Updated ASCO data for ZL-1310…reaffirm its best-in-class potential…With multiple launches ahead…profitability within reach, Zai Lab is executing on its vision to become a leading global biopharma company.” — Dr. Samantha Du .
- “The July update to national MG guidelines further strengthens VYVGART’s role…we expect momentum to accelerate in the second half…With a 28% y/y reduction in operating loss…we are on track to achieve profitability in the fourth quarter.” — Josh Smiley .
- “Bemarituzumab plus chemotherapy demonstrated a statistically significant and clinically meaningful improvement in OS…we plan to move rapidly toward regulatory submission in China.” — Dr. Rafael Amado on FORTITUDE-101 .
Q&A Highlights
- Revenue trajectory and profitability: Management reaffirmed FY25 revenue guidance ($560–$590M) and Q4 adjusted profitability; expects accelerating 2H growth driven by VYVGART and ZEJULA stabilization .
- Bemarituzumab opportunity: ~450k gastric cancer patients in China with ~30% FGFR2b overexpression; management framed a $1B+ potential over time and discussed ocular AEs manageable with monitoring .
- VYVGART inventory and formulation: Q4 2024 channel stocking for Hytrulo; normal inventory build expected 2H25; Hytrulo expected to become a meaningful formulation post NRDL, with PFS submission planned .
- ZL-1310 pivotal plan and partnering: Pursuing accelerated approval path; randomized pivotal to initiate 2H25; Zai Lab plans to self-sponsor while remaining open to partnerships .
- Broader commercial franchise: NUZYRA and XACDURO expected to contribute to 2H growth; XACDURO constrained near-term by supply .
Estimates Context
- Q2: revenue was a significant miss vs consensus; EPS was a beat. Expect models to adjust for lower near-term top-line but stronger operating leverage as SG&A and R&D fall y/y .
- Values retrieved from S&P Global.*
Key Takeaways for Investors
- Mix shift toward VYVGART maintenance use and guideline support should drive 2H acceleration; watch for NRDL progress on subcutaneous Hytrulo and PFS submissions to deepen penetration .
- Despite a revenue miss vs consensus, operating and adjusted losses improved materially y/y; the Q4 adjusted profitability target remains credible given cost discipline and launch readiness .
- ZEJULA softness appears transient amid PARPi dynamics; management expects stabilization and renewed growth in first-line ovarian, supporting base business resilience .
- Pipeline catalysts are stock-moving: bemarituzumab China submission (2H25) and detailed OS data; ZL-1310 pivotal initiation with compelling intracranial activity and favorable safety profile .
- Near-term execution risks: XACDURO supply localization and competitive pressure in PARPi; monitor quarterly trajectory vs guidance and inventory normalization for VYVGART .
- Medium-term thesis: scalable, resource-efficient commercial model for multiple launches (KarXT, bemarituzumab, TTFields) plus global innovation assets (DLL3 ADC, IL-13/IL-31 bispecific) can sustain revenue growth and margin expansion .
- Trading implications: Expect sentiment to hinge on pipeline data flow (bema OS details, DLL3 updates) and confirmation of sequential revenue acceleration; EPS leverage may support downside protection despite top-line volatility .