TheraRadar
Data updated: May 26, 2026

NIVESTYM (filgrastim-aafi)

Oncology Approved 2018-07-20

Nivestym (filgrastim-aafi) is a leukocyte growth factor used to manage neutropenia and reduce the risk of infection in patients with various cancers and blood disorders. It is primarily indicated for patients receiving myelosuppressive or myeloablative chemotherapy, including those undergoing bone marrow transplantation or treatment for acute myeloid leukemia. The drug also serves to mobilize progenitor cells for collection and to treat symptomatic patients with chronic forms of neutropenia, such as congenital, cyclic, or idiopathic types.

Source: FDA Label • Pfizer • Leukocyte Growth Factor

How NIVESTYM Works

Nivestym acts as a colony-stimulating factor by binding to specific receptors on the surface of hematopoietic cells. This binding stimulates the proliferation and differentiation of neutrophil progenitors within the bone marrow, regulating the production of mature neutrophils. Additionally, the drug enhances the functional activation of these cells, increasing their phagocytic ability and antibody-dependent killing to better combat infections.

1
Indication
--
Phase 3 Trials
7
Years on Market

Details

Status
Prescription
First Approved
2018-07-20
Routes
INJECTION, SINGLE-DOSE
Dosage Forms
INJECTABLE, VIAL

Companies

Active Ingredient: FILGRASTIM-AAFI

NIVESTYM Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
16 FDA actions from 2018 to 2024
Feb 2024 SUPPL
Label · Labeling
Aug 2023 SUPPL
Label · Labeling
May 2021 SUPPL
Label · Labeling

What NIVESTYM Treats

6 indications

NIVESTYM is approved for 6 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Febrile Neutropenia
  • Acute Myeloid Leukemia
  • Neutropenia
  • Congenital Neutropenia
  • Cyclic Neutropenia
  • Idiopathic Neutropenia
Source: FDA Label
Biosimilar for Neupogen

NIVESTYM is a lower-cost alternative to Neupogen with no clinically meaningful differences. Requires prescriber approval to substitute.

NIVESTYM Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

What's emerging in NIVESTYM's indications

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Phase 3 candidates targeting molecules with no FDA-approved drug, in indications NIVESTYM treats. First-in-class if their pivotal trials read out positive.

Drugs Similar to NIVESTYM

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Active Pipeline

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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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.

NIVESTYM FDA Label Details

Indications & Usage

FDA Label (PDF)

NIVESTYM is indicated for the treatment of Febrile Neutropenia; Acute Myeloid Leukemia; Neutropenia; Congenital Neutropenia; Cyclic Neutropenia; Idiopathic Neutropenia.

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.