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Ruxotemitide - Lytix Biopharma/Verrica Pharmaceuticals

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Drug Profile

Ruxotemitide - Lytix Biopharma/Verrica Pharmaceuticals

Alternative Names: Cancer-vaccine-Lytix-Biopharma; LTX-315; Oncopore; VP-315; VP-LTX-315

Latest Information Update: 23 May 2025

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At a glance

  • Originator Lytix Biopharma
  • Developer Lytix Biopharma; Verrica Pharmaceuticals
  • Class Adjuvants; Amides; Amines; Antineoplastics; Benzyl compounds; Butylamines; Immunotherapies; Indoles; Peptides
  • Mechanism of Action Cell membrane structure modulators; Immunostimulants
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    No
  • New Molecular Entity Yes

Highest Development Phases

  • Phase II Basal cell cancer; Malignant melanoma; Soft tissue sarcoma
  • Phase I/II Solid tumours
  • No development reported Carcinoma; Triple negative breast cancer

Most Recent Events

  • 14 May 2025 Verrica Pharmaceuticals completes an End-of-Phase II meeting with US FDA for the development of Ruxotemitide for Basal cell cancer
  • 14 Feb 2025 Lytix Biopharma plans a phase III trial for Basal cell cancer
  • 13 Feb 2025 Verrica is preparing for FDA discussions in first half of 2025 to outline the path toward a Phase III trial

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