A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of ABBV-368 Plus Tilsotolimod and Other Therapy Combinations in Participants With Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma

  • STATUS
    Not Recruiting
  • End date
    Nov 25, 2022
  • participants needed
    69
  • sponsor
    AbbVie
Updated on 5 March 2022

Summary

The main objective of this study is to assess safety, tolerability, and pharmacokinetics (PK) of ABBV-368 plus tilsotolimod; ABBV-368 plus tilsotolimod and nab-paclitaxel; and ABBV-368 plus tilsotolimod, nab-paclitaxel, and ABBV-181 in participants with recurrent/metastatic (R/M) head and neck squamous cell carcinoma (HNSCC).

Details
Condition Advanced Solid Tumors Cancer
Treatment Nab-paclitaxel, ABBV-181, ABBV-368, Tilsotolimod
Clinical Study IdentifierNCT04196283
SponsorAbbVie
Last Modified on5 March 2022

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