NCT07088991Recruiting
Clinical and Demographic Characteristics of Adult p Atients With NEurofibromatosis in RUSsia
Clinical and Demographic Characteristics of Adult Patients With NEurofibromatosis in RUSsia
Source: ClinicalTrials.gov · Last updated 25 Sept 2026
Brief summary (registry, in English)
Clinical and Demographic Characteristics of Adult Patients with NEurofibromatosis in RUSsia (NEREUS)
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 200 (estimated)
- First submitted
- 3 Jul 2025
- Start date
- 6 Jun 2025
- Primary completion date
- 31 Mar 2028
- Lead sponsor
- AstraZeneca
- NCT number
- NCT07088991
What you commit to
- Study type: Observational
- Planned participants: 200
- From 6 Jun 2025 to the primary completion date, 31 Mar 2028
- 16 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients with the evidence of a malignant glioma, malignant peripheral nerve sheath tumor, or other cancer, requiring treatment with chemotherapy or radiation therapy.
- Prior receipt of any MEK-inhibitor for PN therapy within 4 months before screening or initiation of therapy prior to age 18 verified by medical records/histories (e.g., prior prescriptions, hospitalization data).
- Patients who modify their index pathogenetic therapy regimen during the study (for example, pathogenetic antitumor therapy of PN; switching to a different therapy), as determined by the investigator at any protocol-specified visit during the a study, will be excluded from the primary efficacy analysis population from the point of modification onward and will not continue study participation.
Other
- The participation in any clinical study currently (patients participating in other non-interventional studies may be included);
- In the opinion of the investigator the patient is not able to return for follow-up visits or obtain required follow-up studies.
- Individuals who are pregnant or breast feeding or who become pregnant while enrolled on this trial, if they are unable to undergo radiographic evaluations or MRI scans requested for research purposes, or other studies which might negatively impact on the pregnancy.
Who the study is looking for
- Age ≥ 18 years at the time of inclusion.
- Signed and dated written informed consent in accordance with ICH-GCP and local law prior to inclusion in the study.
- NF1 diagnosed (according to the international consensus criteria for evaluating NF1 \[18\]), see Appendix A.
- Confirmed PN by clinical assessment, USI, MRI, biopsy; one method is sufficient (histologic confirmation of PN is not necessary in the presence of radiographic findings).
- Existing of PN-associated symptoms.
- Adult patients (≥18 years) with newly diagnosed PN or established PN naïve to MEK-inhibitor therapy verified by medical records/histories (e.g., prior prescriptions, hospitalization data).
Sex: All · Does not accept healthy volunteers
Sites (16)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.