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Clinical trial to investigate safety and tolerability of TransCon IL-2 in adult participants with malignant solid tumors

THE OBJECTIVE OF THIS RESEARCH IS TO LEARN ABOUT THE EFFECTS OF AN EXPERIMENTAL DRUG CALLED TRANSCON IL-2 SS/? WHEN ADMINISTERED ALONE OR IN COMBINATION WITH PEMBROLIZUMAB, CHEMOTHERAPY ET OR TRANSCON TLR7/8 AGONIST, OR IN COMBINATION WITH PEMBROLIZUMAB AND CHEMOTHERAPY ET.

Cancer Center
Status
In recruitment
headquarters
Pamplona/Madrid

Technical Summary

  • PHASE I/II, OPEN-LABEL, DOSE-ESCALATION AND DOSE-EXPANSION STUDY TO INVESTIGATE THE SAFETY AND TOLERABILITY OF TRANSCON IL-2 SS/? ALONE OR IN COMBINATION WITH PEMBROLIZUMAB, STANDARD CHEMOTHERAPY OR TRANSCON TLR7/8 AGONIST, OR IN COMBINATION WITH PEMBROLIZUMAB AND STANDARD CHEMOTHERAPY, IN ADULT PARTICIPANTS WITH LOCALLY ADVANCED OR METASTATIC MALIGNANT SOLID TUMORS
  • Code EudraCT: 2022-001191-34
  • Protocol number: ASND0029
  • Promoter: Ascendis Pharma Oncology Division S/A
  • Molecule/Drug: TransCon IL-2

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

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