Corporate presentation
Logotype for Helus Pharma

Helus Pharma (HELP) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Helus Pharma

Corporate presentation summary

29 Jun, 2026

Strategic focus and pipeline highlights

  • Advancing two proprietary clinical programs, HLP003 and HLP004, targeting major depressive disorder (MDD) and generalized anxiety disorder (GAD), both with positive Phase 2 safety and efficacy results.

  • HLP003 has received FDA Breakthrough Therapy Designation and is in Phase 3 for adjunctive MDD treatment; HLP004 is in Phase 2 for GAD.

  • Pipeline includes potential expansion into additional mental health indications with high unmet need, affecting over 200 million people in the U.S.

  • Over 350 patents filed, with more than 100 granted, providing protection until at least 2041.

  • Cash position of $157.3 million as of March 31, 2026, with a $50 million offering completed in June 2026.

HLP003 (MDD) clinical and pharmacological profile

  • Demonstrated rapid, robust, and durable antidepressant effects in Phase 2, with 100% response and 71% remission at 12 months after two 16 mg doses.

  • Favorable safety profile: all adverse events mild to moderate, no suicidality or serious adverse events at 12 months.

  • Deuterated psilocin design offers improved delivery, higher plasma and brain levels, rapid onset (15 min), and consistent effects compared to psilocybin.

  • Phase 3 pivotal program (PARADIGM) underway, with topline data expected Q4 2026.

  • Strong IP and regulatory exclusivity, with patent protection and NCE exclusivity extending to at least 2041.

HLP004 (GAD) clinical and pharmacological profile

  • Positive Phase 2 results in moderate-to-severe GAD: rapid, robust, and durable symptom relief, with -10 point HAM-A reduction at 6 weeks and effects sustained for at least 6 months.

  • Up to 70% responders and 40% remitters at 6 months after a single treatment cycle.

  • Favorable safety profile: all adverse events mild or moderate, no drug-related serious adverse events or suicidality.

  • Intramuscular administration allows rapid discharge (within 3 hours), supporting scalability in clinical practice.

  • Over 90 issued patents, including composition of matter IP through 2041.

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