Sponsor Overview
Explore verified public information about Lokon Pharma AB's expanded access programs, compassionate use policies, and patient eligibility pathways. This report aggregates official statements, independent research, and regulatory data to help patients, providers, and sponsors collaborate efficiently.
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ClinicalTrials.gov data sources power this status.
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Expanded Access Intelligence
Official Statements
Score contribution: 100 — 1 supporting sources.
“Lokon does not provide investigational drugs to patients outside the clinical trial context. However, for patients who previously responded to a Lokon investigational drug within a clinical trial (as defined in the study protocol), and who may benefit from treatment continuation, the treating physician may request expanded access to the Lokon investigational drug. “Expanded Access” refers to the use of an investigational product outside of a clinical trial, for the potential treatment of a serious or life-threatening condition, and different regulations apply in different countries. Hence, a case-by-case evaluation must be completed prior to an expanded access decision for individual patient use by Lokon Pharma. In the US, an Individual Patient Expanded Access (also referred to as single patient) application can be filed by the treating physician.”
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