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Clinical Trial Summary

The purpose of this Medical Access Program (also referred to as an Expanded Access Program in the USA) is to provide access to Dato-DXd for eligible patients with previously treated advanced or metastatic nonsquamous non-small cell lung cancer (NSCLC) who, in their treating physician's opinion, have an unmet clinical need, are unlikely to obtain optimal benefit from currently approved and commercially available drugs, and who cannot enter a suitable clinical trial.


Clinical Trial Description

This is a Medical Access Program that will be available to adult patients in the USA with previously treated advanced or metastatic nonsquamous NSCLC who have no suitable treatment options and are not able to enter a clinical trial. Patients enrolled in the Medical Access Program can continue treatment until any of the following occurs: - Disease progression - Unacceptable toxicity - The benefit-risk no longer favors the individual - Dato-DXd becomes commercially available and reimbursement is approved - The patient chooses to discontinue treatment - Withdrawal of consent - Pregnancy - Physician discretion - Death Patients enrolled in the Medical Access Program have an option to participate in collection of safety-focused clinical practice data. This will contribute towards better understanding of the clinical experience of treatment with Dato-DXd. Participation in this optional data collection will have no bearing on receipt of treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06279728
Study type Expanded Access
Source Daiichi Sankyo
Contact Contact for Program Information
Phone 908-992-6400
Email patient.access@bionicalemas.com
Status Available
Phase

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