Condition: Advanced Solid Tumors · Metastatic Solid Tumors · Sponsor: Chong Kun Dang Pharmaceutical
The purpose of this first-in-human (FiH) study is to assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of CKD-512 given alone and in combination with pembrolizumab in subjects with advanced or metastatic solid tumors who have failed all standard available therapy.
This description comes directly from the study's public registry record.
Contact details are listed per location below or on the registry record.
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| Severance Hospital, Yonsei University Health System | Seoul, South Korea | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07215637