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Data updated: May 26, 2026

FULPHILA (pegfilgrastim-jmdb)

Oncology Approved 2018-06-04

Fulphila is a leukocyte growth factor indicated to reduce the risk of infection in patients with non-myeloid malignancies. It is specifically used to decrease the incidence of febrile neutropenia in individuals undergoing myelosuppressive chemotherapy associated with a significant risk of this condition. The drug is not intended for the mobilization of peripheral blood progenitor cells for hematopoietic stem cell transplantation.

Source: FDA Label • Viatris • Leukocyte Growth Factor

How FULPHILA Works

Fulphila belongs to a class of drugs known as colony-stimulating factors that target hematopoietic cells. The medication functions by binding to specific receptors located on the surface of these cells. This binding action stimulates the proliferation, differentiation, commitment, and functional activation of the cells to support the immune system.

1
Indication
--
Phase 3 Trials
7
Years on Market

Details

Status
Prescription
First Approved
2018-06-04
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: PEGFILGRASTIM-JMDB

FULPHILA Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
5 FDA actions from 2018 to 2023
Oct 2023 SUPPL
Label · Labeling
Mar 2021 SUPPL
Label · Labeling
May 2019 SUPPL
Label · Labeling

What FULPHILA Treats

2 indications

FULPHILA is approved for 2 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Febrile Neutropenia
  • Non-Myeloid Malignancies
Source: FDA Label
Biosimilar for Neulasta

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

FULPHILA 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 FULPHILA's indications

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

Drugs Similar to FULPHILA

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FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

GRANIX
TBO-FILGRASTIM
2 shared
SICOR BIOTECH
Shared indications:
Febrile NeutropeniaNon-Myeloid Malignancies
RYZNEUTA
EFBEMALENOGRASTIM ALFA-VUXW
2 shared
EVIVE BIOTECHNOLOGY
Shared indications:
Febrile NeutropeniaNon-Myeloid Malignancies
ARMLUPEG
PEGFILGRASTIM-UNNE
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Lupin
Shared indications:
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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.

FULPHILA FDA Label Details

Indications & Usage

FDA Label (PDF)

FULPHILA is indicated for the treatment of Febrile Neutropenia; Non-Myeloid Malignancies.

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Data Sources

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