The purpose of this trial is to evaluate the safety and efficacy of TransCon TLR7/8
Agonist, TransCon IL-2 β/γ, and pembrolizumab given prior to curative intent surgery in
treatment of participants with newly diagnosed Stage III/IVA resectable locoregionally
advanced head and neck squamous cell carcinoma (LA-HNSCC). After surgery, participants
will receive local standard-of-care treatment and will be followed for safety, efficacy,
and survival for up to 2 years.
This trial contains a safety run-in to evaluate the safety and tolerability of the two
treatment arms: Arm A (TransCon TLR7/8 Agonist plus pembrolizumab) and Arm B (TransCon
TLR7/8 Agonist plus TransCon IL-2 β/γ). The safety run-in will be followed by the
randomized Phase 2, open-label part of the trial comparing the safety, efficacy and
survival of treatment Arm A or Arm B compared to treatment Arm C (pembrolizumab
monotherapy).
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05980598.
This is a randomized, Phase 2, open-label, multicenter trial of TransCon TLR7/8 Agonist
in combination with pembrolizumab, TransCon TLR7/8 Agonist in combination with TransCon
IL-2 β/γ, or pembrolizumab monotherapy as neoadjuvant therapy in participants with Stage
III-IVA resectable LA-HNSCC.
This trial starts with a safety run-in of 12 participants, 6 participants each in Arms A
(TransCon TLR7/8 Agonist plus pembrolizumab) and B (TransCon TLR7/8 Agonist plus TransCon
IL-2 β/γ) randomized 1:1.
After completing the safety run-in, 80 participants will be randomized in a 2:2:1 ratio
in 3 treatment Arms A, B or C (pembrolizumab monotherapy).
Once randomized, participants should begin treatment within 5 calendar days. Participants
enrolled after the safety run-in, into the 2:2:1 randomization part of the trial, will be
stratified as follows: oropharyngeal HPV p16 positive versus oropharyngeal HPV p16
negative or larynx/hypopharyngeal/oral cavity regardless of HPV p16 status. All
participants should receive study drug(s) every 21 days (Q21D) for 2 cycles followed by
curative-intent surgery. After surgery, participants may receive standard-of-care
treatment in the adjuvant setting, as per investigator's decision and local guidelines.
Lead OrganizationAscendis Pharma A/S
Principal InvestigatorJoan Diane (Chopik) Morris