10-Q · May 13, 2026
Alto Neuroscience's Q1 2026 filing reveals a continued net loss of $26.2 million, with a diluted EPS at -$0.80, which signifies a widening loss compared to $15.2 million in the same quarter last year. The company…
Earnings analysis · 10-Q
Filed August 12, 2026 · Our reading of the company's report
The latest report
Alto remains a development-stage biotechnology company with no product revenue and expanding losses, as second-quarter net loss rose 56% year over year to $27.638 million and operating expenses increased to $29.129…
Alto remains a development-stage biotechnology company with no product revenue and expanding losses, as second-quarter net loss rose 56% year over year to $27.638 million and operating expenses increased to $29.129 million from $18.682 million. The principal positive is a substantially improved funding position following the July offering, with $244.2 million of cash, cash equivalents and restricted cash at June 30 plus approximately $94.6 million of offering proceeds. Clinical execution remains the key value driver, particularly the expanded ALTO-207 program, but rising R&D spending, continued negative cash flow and the need for future financing temper the outlook.
Our analysis across the last few reports.
Our model's reading of each filing, not the share price or the market's reaction. Annual and quarterly reports each occupy one position.
Cash, cash equivalents and restricted cash increased to $244.2 million at June 30, 2026 from $177.0 million at December 31, 2025. The July 2026 Offering added approximately $94.6 million of net proceeds and management believes funding is sufficient for at least the next 12 months.
ALTO-207 Phase 2b enrollment was initiated in April 2026, with approximately 178 adults planned for the trial. Management expects topline data in the second half of 2027 and plans an adjunctive Phase 3 trial by early 2027.
ALTO-101 showed directional or statistically significant effects on several EEG measures in follow-up analyses, including individual alpha peak frequency with d=0.59 and p=0.001, and sustained attention with d=0.41 and p=0.02.
Operating cash use was $46.9 million in the six months ended June 30, 2026, versus $30.3 million in the prior-year period, while financing provided $114.7 million, primarily from the 2026 private placement.
The company continues to advance seven clinical-stage assets across major depressive disorder, bipolar depression, treatment-resistant depression, schizophrenia and Parkinson’s disease.
Second-quarter net loss increased to $27.638 million from $17.706 million year over year, while six-month net loss rose to $53.875 million from $32.875 million. Management expects operating losses and negative operating cash flows to continue for the foreseeable future.
Research and development expense increased to $22.108 million from $13.124 million year over year, led by approximately $6.4 million of incremental ALTO-207 spending. Management expects R&D expenses to increase substantially as programs move into later-stage trials.
The company has not generated revenue from product sales and does not expect product-sales revenue for several years, if at all. Management states that substantial additional funding will be needed, and inadequate funding could force delays, reductions or elimination of development programs.
The ALTO-101 Phase 2 proof-of-concept trial did not achieve statistical significance on its primary EEG or cognitive endpoints; the overall study included 83 patients and the theta-ITC result was near-significant at p=0.052.
The company had $15.0 million of outstanding principal under its Amended Loan Agreement at June 30, 2026. The interest-only period ends January 1, 2027, after which the term loan is repaid in equal monthly payments through January 1, 2029.
The filing states there were no material changes to the risk factors disclosed in the Annual Report. Nonetheless, the company estimates a remaining headquarters lease commitment of $5.6 million through March 2030, creating an additional fixed cash obligation.
No quantitative revenue or EPS guidance was provided. Management expects ALTO-207 Phase 2b topline data in the second half of 2027, an adjunctive TRD Phase 3 trial by early 2027, and a monotherapy TRD Phase 3 trial in the second half of 2027; ALTO-300 topline data are expected in the first half of 2027 and ALTO-100 topline data in mid-2027.
Alto Neuroscience's Q1 2026 filing reveals a continued net loss of $26.2 million, with a diluted EPS at -$0.80, which signifies a widening loss compared to $15.2 million in the same quarter last year. The company…
Alto is a clinical‑stage precision psychiatry company advancing a seven‑asset pipeline using a proprietary biomarker Platform. Clinical programs ALTO‑300 and ALTO‑207 show replicated biomarker signal and encouraging…
Alto reported no product revenue and a lower quarterly operating loss as operating expenses fell to $14,951 for the three months ended September 30, 2025 (down from $18,886). Net loss improved to $14,181 (GAAP EPS…
Alto reported Q2 2025 net loss of $17.706M (three months) and GAAP diluted EPS of -$0.65, wider than Q2 2024 loss of $16.030M and EPS -$0.60 and missing the consensus estimate of -$0.57 (−14.04%). There was no product…
This is our reading of a public filing, not the filing itself. Analysis can contain errors; check the source document for full context.