Alto Neuroscience (ANRO) TD Cowen 6th Annual Novel Mechanisms in Neuropsychiatry Summit summary
Event summary combining transcript, slides, and related documents.
TD Cowen 6th Annual Novel Mechanisms in Neuropsychiatry Summit summary
23 Sep, 2026ALTO-207 program overview
ALTO-207 combines pramipexole and ondansetron to address tolerability issues, enabling higher and faster dosing for treatment-resistant depression (TRD).
Real-world use of pramipexole is limited by slow titration due to nausea, but efficacy is strong, especially for anhedonia.
The phase II-B trial uses a custom titration pack to reach a 3.2 mg pramipexole target, with most patients expected to tolerate this dose.
The trial is powered conservatively, aiming for a Cohen's d of 0.45, with dropout rates expected to align with industry standards.
Safety monitoring focuses on nausea, impulse control disorders, and QTc prolongation, with measures in place to minimize risks.
Clinical development and timelines
Enrollment for the phase II-B ALTO-207 trial is on track, with top-line data expected in the second half of next year.
Plans are in place to initiate phase III trials for both adjunctive and monotherapy use before phase II-B readout, pending FDA alignment.
Flexibility exists to adjust phase III design based on phase II-B results, particularly regarding sample size.
The program aims to provide a differentiated, take-home treatment option for a broad range of TRD patients.
Efforts are underway to validate anhedonia scales for potential inclusion in labeling and publications.
Broader pipeline updates
ALTO-300 (agomelatine) is in phase II-B for adjunctive MDD treatment, with a biomarker-enriched design and top-line data expected in the first half of next year.
ALTO-100 targets bipolar depression with a pro-neuroplasticity mechanism, focusing on patients with learning and memory impairments; readout is anticipated mid-2027.
Both programs have implemented rigorous patient eligibility and compliance checks to ensure high-quality data.
Advancement to phase III for these programs depends on achieving statistical significance on MADRS change and demonstrating good tolerability.
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