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Phase I/II, open-label study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of CLN 081 in patients with non-small cell lung carcinoma

THE AIM OF THIS STUDY IS TO EVALUATE A NEW EXPERIMENTAL DRUG, CALLED CLN-081, IN PARTICIPANTS WITH NON-SMALL CELL LUNG CARCINOMA.

Status
In recruitment
headquarters
Pamplona/Madrid

Technical Summary

  • PHASE I/II, OPEN-LABEL, MULTICENTER STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS, PHARMACODYNAMICS AND EFFICACY OF CLN 081 IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC NON-SMALL CELL LUNG CARCINOMA WITH EGFR EXON 20 INSERTIONAL MUTATIONS WHO HAVE RECEIVED PRIOR SYSTEMIC CHEMOTHERAPY WITH A PLATINUM DERIVATIVE
  • Code EudraCT: 2019-002409-23
  • Protocol number: CLN-081-001
  • Promoter: Cullinan MICA Corp.
  • Molecule/Drug: CLN 081

* 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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