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Ruxotemitide - Lytix Biopharma

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Drug Profile

Ruxotemitide - Lytix Biopharma

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

Latest Information Update: 04 Sep 2024

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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

  • 29 Aug 2024 Lytix Biopharma plans the phase II NeoLIPA (ATLAS-IT-06) trial for Malignant melanoma (Neoadjuvant therapy, Combination therapy) in Norway (Intratumoural, Injection), in third quater of 2024 (Lytix Biopharma pipeline, October 2023)
  • 14 Aug 2024 Verrica Pharmaceuticals plans an End-of-Phase 2 meeting with US FDA to determine next steps for the development of Ruxotemitide for Basal cell cancer in the first half of 2025
  • 14 Aug 2024 Updated efficacy and adverse events data from a phase II trial in Basal cell cancer released by Verrica Pharmaceuticals

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