Luye Pharma USA in partnership with
APA 2026 · Partner Brief

Ansofaxine

Luye Pharma USA is showcasing Ansofaxine at APA 2026. Here's the context, what to ask at the booth, and where Videra fits in the conversation.

CompanyLuye Pharma USA
StatusPhase 3 (completed primary endpoints)
IndicationMajor Depressive Disorder
MechanismSerotonin-norepinephrine-dopamine reuptake inhibit…
Context

Why Luye Pharma USA is promoting this at APA

Ansofaxine is Luye's pipeline highlight — the first triple reuptake inhibitor with positive Phase 3 data (74-80% response rate, 52% remission). At APA, they'll be building KOL awareness ahead of an expected NDA filing. The clean tolerability profile (no sexual dysfunction, no weight gain reported) is a major differentiator vs. SSRIs/SNRIs for psychiatrists tired of managing those side effects.

Booth Conversation

Talking points for the conversation

Ask about: NDA filing timeline; tolerability profile data in detail (sexual dysfunction rates, weight changes); how they position vs. SNRIs (what does dopamine reuptake inhibition add clinically?); target patient profile; Phase 3 response/remission rate details. The tolerability story is incredibly compelling for psychiatrists.

Videra · Med Affairs Angle

Where Videra fits

First SNDRI needs differentiated evidence — VoiceVitals can objectively capture the anhedonia, motivation, and energy improvements that dopamine reuptake inhibition should uniquely deliver (beyond what SNRIs provide). ePRO+ enriches the NDA-stage evidence. The tolerability advantage (no sexual dysfunction, no weight gain) can be captured through multimodal patient-reported outcomes — real-world evidence that matters enormously to prescribers.

Let's pick this up at the booth.

Set up a follow-up with Luye Pharma USA's team and Videra Health.

Email Ryan Roberts →