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Athira Pharma, Inc. (ATHA)·Q2 2025 Earnings Summary
Executive Summary
- Q2 2025 was operationally tight with no revenue and materially lower operating expenses; net loss improved to $7.0M (−$0.18 EPS) vs $9.1M in Q1 and $26.9M YoY, driven by the wind-down of fosgonimeton and a leaner cost base .
- Reported EPS of −$0.18 beat the split-adjusted S&P Global consensus of −$1.40 on a post–10-for-1 basis (reported −$0.18 → −$1.80 split-adjusted) due to lower-than-expected OpEx; revenue remained $0 .
- Cash, cash equivalents and investments were $29.8M at quarter-end, down from $36.7M in Q1 and $51.3M at YE 2024, reflecting ongoing R&D and corporate spending while the company explores strategic alternatives .
- Near-term catalysts: clarity on strategic alternatives/partnering and initiation plans for an ALS patient trial of ATH-1105; the September reverse split was intended to support Nasdaq compliance and broaden investor appeal .
What Went Well and What Went Wrong
What Went Well
- Significant OpEx reduction: total operating expenses fell 24% sequentially ($9.54M → $7.29M) and 74% YoY ($28.03M → $7.29M), reflecting disciplined cost control post-fosgonimeton .
- Pipeline progress: Phase 1 ATH-1105 safety/PK data showed favorable tolerability, dose proportional PK, and CNS penetration, supporting continued development; management reiterated readiness to initiate an ALS patient trial subject to strategic options .
- CEO tone on ALS focus and partnering: “We have substantially completed preparation activities to enable initiation of a future clinical trial in people living with ALS… by us or in conjunction with a partner” .
What Went Wrong
- No revenue: as a clinical-stage company, Athira reported no product revenue; losses continue albeit reduced .
- Cash burn remains material: net cash used in operations was $21.7M for 6M’25 (vs $48.1M 6M’24), still significant given the $29.8M cash+investments balance .
- Strategic uncertainty: formal exploration of strategic alternatives continues, and development of fosgonimeton remains paused, limiting portfolio breadth and visibility .
Financial Results
Core P&L and Balance Metrics
Notes:
- No revenue reported; statements of operations present only operating expenses and other income, consistent with clinical-stage status .
Actual vs Consensus (Q2 2025)
Values marked with * were retrieved from S&P Global.
KPIs
Segment breakdown: Not applicable; Athira has no commercial segments .
Guidance Changes
Earnings Call Themes & Trends
No Q2 2025 earnings call transcript was available via our document search [List: earnings-call-transcript none]. The themes below reflect prepared remarks and press releases.
Management Commentary
- CEO (Q2 PR): “We have substantially completed preparation activities to enable initiation of a future clinical trial in people living with ALS by us or in conjunction with a partner… We look forward to providing an update regarding our plans in the near future.”
- CEO (Q1 PR): “We continue to focus our efforts on advancing ATH-1105… keeping us on-track to enable dosing ALS patients in late 2025.”
- CMO (Aug 14 PR): “Our Phase 1 safety, tolerability, and pharmacokinetic data are encouraging and support continued development of ATH-1105.”
Q&A Highlights
- No Q2 2025 earnings call transcript was identified, so no Q&A highlights or clarifications are available [List: earnings-call-transcript none].
Estimates Context
- S&P Global consensus for Q2 2025 EPS was −$1.40 (two estimates); revenue $0.0 (two estimates). Reported EPS of −$0.18 equates to −$1.80 on a split-adjusted basis (10-for-1), implying a modest beat versus consensus due to lower OpEx; revenue in line at $0.0* .
- Target price consensus mean was $4.00 (one estimate); formal consensus recommendation text unavailable*.
Values marked with * were retrieved from S&P Global.
Key Takeaways for Investors
- Cost discipline is the story: OpEx down 24% q/q and 74% y/y, narrowing quarterly losses and enabling an extended runway for ATH-1105 execution .
- ATH-1105 continues to de-risk: Phase 1 HV data support safety/PK and CNS penetration; company-ready logistics for ALS patient trial initiation await strategic path/partner clarity .
- Strategic alternatives remain the swing factor: expect updates that could impact capital needs, trial design, and timeline; partnering could reduce burn and accelerate development .
- Capital structure adjustment: the September reverse split supports Nasdaq compliance and potential investor reach; model EPS on a split-adjusted basis for estimate comparisons .
- Near-term watch items: ALS trial initiation timing, partnering announcements, OpEx trajectory into 2H25, and cash burn vs $29.8M cash+investments at Q2-end .
- Estimate revisions: modest EPS improvements vs consensus on a split-adjusted basis may prompt slight upward adjustments to near-term loss forecasts; revenue remains at $0 absent partnering revenue*.
Values marked with * were retrieved from S&P Global.