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Safety and Efficacy of VB10.16 and Pembrolizumab in Patients With Head-Neck Squamous Cell Carcinoma

StatusRecruiting
PhasePhase 1/2
Started2023-12-19
View on ClinicalTrials.gov ↗
This is a multi-center study in patients with un-resectable Recurrent or Metastatic HPV16-positive oropharyngeal Head and Neck Squamous Cell Carcinoma (HNSCC). The trial is designed to investigate VB10.16, an investigational therapeutic DNA vaccine in combination with another medicine, pembrolizumab, which is the standard of care for patients with previously untreated metastatic or resectable recurrent PD-L1 positive HNSCC. The study is divided in 2 parts: * Phase 1: Dose escalation to evaluate safety and determine the recommended phase 2 dose (RP2D) of VB10.16 * Phase 2: Randomized comparison of VB10.16 in combination with pembrolizumab versus pembrolizumab monotherapy The goal of Phase 1 is to evaluate the safety and tolerability of the combined treatment and to decide on the dose of VB10.16 to be used in the second part of the trial. The randomized Phase 2 will consist of 2 parallel arms exploring VB10.16 at the selected RP2D from the escalation phase in combination with pembrolizumab SoC (experimental arm, Arm A), versus pembrolizumab alone (control arm, Arm B).

Amendment history 5 changes detected by DataLookout

2026-08-27
critical
Primary endpoint(s) modified
WasPhase 1+2: Full trial: Objective Response Rate (ORR), Phase 1+2: Full trial: Objective Response Rate (ORR), Phase 1: Dose Escalation: Dose Limiting Toxicities (DLT), Phase 2: Dose Expansion: AEs, Phase 2: Dose Expansion: Discontinuation due to adverse reaction, Phase 2: Dose Expansion: Immune response, Phase 2: Dose Expansion: Objective Response Rate (ORR)
NowPhase 1: Dose Escalation: Dose Limiting Toxicities (DLT), Phase 2: Dose Expansion: Progression-Free Survival (PFS), Phase 2: Dose expansion: Objective Response Rate (ORR)
2026-08-27
notable
Enrollment increased: 51 → 110 participants
2026-08-27
minor
Trial sites reduced: 17 → 12 locations
2026-08-27
critical
Primary completion pushed: 2027-09 → 2029-01
2026-08-27
minor
Completion pushed: 2028-01 → 2030-12
Trial Details
NCT Number NCT06016920
Lead Sponsor Nykode Therapeutics ASA
Collaborators: Merck Sharp & Dohme LLC
Conditions HPV Positive Oropharyngeal Squamous Cell Carcinoma, HNSCC
Enrollment 110 participants
Start Date 2023-12-19
Primary Completion 2029-01 (estimated)
Study Completion 2030-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-26