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Individual Patient Compassionate Use of Mirdametinib

Status
AVAILABLE
Phases
Unknown
Study type
Expanded Access
Source
ClinicalTrials.gov
Registry ID
NCT05028166
Enrollment
Unknown
Registered
2021-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Histiocytic Neoplasm, Neurofibromatosis Type 1-Associated Plexiform Neurofibromas, Other MAP-K Pathway Driven Diseases

Keywords

RASopathies, NF1, Neurofibromatosis, Plexiform Neurofibromas, Langerhans

Brief summary

This program is being offered on a patient by patient basis and will require company, Institutional Review Board/Independent Ethics Committee, and applicable competent authority approval.

Interventions

Patients will receive oral mirdametinib.

Sponsors

SpringWorks Therapeutics, Inc., a healthcare company of Merck KGaA, Darmstadt, Germany
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
2 Years to No maximum

Inclusion criteria

* Patient has a serious, debilitating or life-threatening medical condition that cannot be treated satisfactorily with an authorized medicinal product or other available standard treatment options, or all other treatment options have been exhausted. * Patient does not qualify to participate in an ongoing clinical trial.

Contacts

CONTACTUS Medical Information
eMediUSA@emdserono.com888-275-7376

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026