STIMUFEND
Stimufend is a leukocyte growth factor indicated to decrease the incidence of infection, as manifested by febrile neutropenia, in patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs. It is also approved to increase survival in patients acutely exposed to myelosuppressive doses of radiation, a condition known as Hematopoietic Subsyndrome of Acute Radiation Syndrome. The drug is not indicated for the mobilization of peripheral blood progenitor cells for hematopoietic stem cell transplantation.
How STIMUFEND Works
Stimufend is a colony-stimulating factor that acts on hematopoietic cells by binding to specific cell surface receptors. This binding process stimulates the proliferation, differentiation, and commitment of these cells. Furthermore, the mechanism facilitates the functional activation of end cells to support the immune system.
Details
- Status
- Prescription
- First Approved
- 2022-09-01
- Routes
- INJECTION
- Dosage Forms
- SOLUTION
STIMUFEND Approval History
What STIMUFEND Treats
2 indicationsSTIMUFEND is approved for 2 conditions since its original approval in 2022. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Febrile Neutropenia
- Acute Radiation Syndrome
STIMUFEND is a lower-cost alternative to Neulasta with no clinically meaningful differences. Requires prescriber approval to substitute.
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Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
STIMUFEND FDA Label Details
ProIndications & Usage
FDA Label (PDF)Stimufend is a leukocyte growth factor indicated to decrease the incidence of infection, as manifested by febrile neutropenia, in patients with non-myeloid malignancies receiving myelosuppressive anti-cancer drugs associated with a clinically significant incidence of febrile neutropenia. Increase survival in patients acutely exposed to myelosuppressive doses of radiation (Hematopoietic Subsyndrome of Acute Radiation Syndrome). Limitations of Use Stimufend is not indicated for the mobilization of peripheral blood progenitor cells for hematopoietic stem cell transplantation. 1.1 Patients with Ca...
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.