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TransCon (TC) TLR7/8 Agonist, TC IL-2 β/γ, Pembrolizumab Prior to Surgery for Advanced Head and Neck Squamous Cell Carcinoma

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NCT05980598

Sponsored by Ascendis Pharma A/S (industry) · ASND — their whole pipeline →.

Phase
Phase 2
Status
Terminated
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
27actual
Sites
65
Countries
Georgia, Germany, Hungary +5

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

The Sponsor made the decision to close enrollment as part of a strategic portfolio review.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-09-29actualWhen the study began enrolling
Primary completion2025-03-28actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-28actualThe whole study's end, after follow-up
First posted2023-08-08actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-08-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Head and Neck Neoplasms

Interventions

  • Drug: TransCon TLR7/8 Agonist
  • Drug: Pembrolizumab — also filed as Keytruda™
  • Drug: TransCon IL-2 β/γ

Primary outcome

what the primary-completion date above is the date OF
Major Pathological Response
measured Up to 6 weeks after Cycle 2 (each cycle is 21 days)

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