BLASUBCUTANEOUSSOLUTION
Approved
Feb 2022
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
2/8 — Basic
Drug data last refreshed 1h ago · AI intelligence enriched 1mo ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
RELEUKO (filgrastim) is a leukocyte growth factor approved in February 2022 by Kashiv BioSciences as a biologic solution for subcutaneous injection. Filgrastim stimulates the production and release of neutrophils from bone marrow, addressing chemotherapy-induced neutropenia and other neutropenic conditions. The drug is a recombinant human granulocyte colony-stimulating factor (G-CSF) analog.
Peak
RELEUKO operates in a mature, competitive G-CSF market with moderate competitive pressure (30%), suggesting a focused manufacturing and operational team rather than rapid commercial expansion.
Mechanism of Action
Pharmacologic Class:
Leukocyte Growth Factor
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Topefilgrastim Injection in the Treatment of High-Risk Pregnant Patients With Preeclampsia
Started Jan 2026
100 enrolled
Preeclampsia
Safety, Tolerability, and PK/PD of Telpegfilgrastim Injection in Non-pregnant Females of Childbearing
Started Apr 2025
18 enrolled
Preeclampsia
Pharmacokinetic, Immunogenicity, and Safety Evaluation of Pegfilgrastim TPI-120 in Healthy Adults
Started Apr 2025
180 enrolled
Healthy Volunteer
Safety, Tolerability, and PK/PD of Telpegfilgrastim in Premenopausal Non-pregnant Females
Started Mar 2025
18 enrolled
Preeclampsia
Reducing Neutropenia Incidence With Pegfilgrastim Administration on Day 3 After Chemotherapy
Started Nov 2023
100 enrolled
Breast Neoplasms
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.