About this trial
This is a single arm, multicenter and prospective study to evaluate the efficacy and safety of T-DXd for the treatment in locally advanced, unresectable, or metastatic participants with selected HER2 positive (IHC 3+) NSCLC which are not eligible for curative therapy
Eligibility criteria
Qualifiers
Male and female participants must be at least 18 years of age at the time of signing the ICF.
Histologically documented Stage III locally advanced and unresectable non-squamous NSCLC not amenable to curative surgery or radiation and/or Stage IV NSCLC.
Participants must have HER2 overexpression (IHC 3+).
progressed following at least one or two prior systemic treatment.
Disqualifiers
Has spinal cord compression or clinically active central nervous system metastases.
Corrected QT interval (QTcF) prolongation to > 470 msec (females) or >450 msec (males) based on average of the screening triplicate12-lead ECG.
History of (non-infectious) ILD / pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening.
Uncontrolled infection requiring systemic antibiotics, antivirals, or antifungals
Trial design
Treatments tested in this trial
- Experimental Group
Treatment groups
Locations
Sponsors and collaborators
Hunan Province Tumor Hospital
Lead sponsor