The purpose of this study is to evaluate the effectiveness, safety of selumetinib and patient's parameters of symptomatic inoperable PN NF1 in real clinical practice in Russia
Age range
3 Years – 18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
ORR in patients receiving selumetinib according to REiNS criteria
Timeframe: from the FSI date (21 Mar 2023) till 36 months from FSI
Best objective response on selumetinib treatment
Timeframe: from the FSI date (21 Mar 2023) till 36 months from FSI
Time to discontinuation of selumetinib
Timeframe: from the FSI date (21 Mar 2023) till 36 months from FSI
Description of diagnostic algorithms for PN NF1 in Russia
Timeframe: from the FSI date (21 Mar 2023) till 36 months from FSI
Reasons for discontinuation of selumetinib
Timeframe: from the FSI date (21 Mar 2023) till 36 months from FSI