drugset / Trial / NCT05329532

Modi-1 Moditope in Breast, Head and Neck, Ovarian, or Renal Cancer

NCT05329532 ↗

Phase 1/2 Recruiting 168 enrolled Scancell Ltd
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main objectives of this study are to assess the safety, tolerability, immunological activity, and preliminary efficacy of the Modi-1 Moditope vaccine, both as monotherapy and in combination with a checkpoint inhibitor (CPI) such as pembrolizumab or nivolumab with or without Ipilimumab (where these are standard of care in a non-neoadjuvant setting), in patients with advanced triple negative breast cancer (TNBC), advanced/unresectable human papillomavirus-negative squamous cell carcinoma of the head and neck (SCCHN), high grade serous ovarian carcinoma (HGSOC), or renal cell carcinoma (RCC). Modi-1 Moditope will also be investigated in the neoadjuvant setting for patients with SCCHN undergoing curative intent surgical resection in combination with pembrolizumab versus the Modi-1 alone.

Timeline

Start
2022-04-07
Primary completion
2026-07-01
Completion
2027-07-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Modi-1 Moditope Vaccine — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous