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Mecapegfilgrastim

Alternative Names: mecapegfilgrastim
Latest Update: 2024-11-12
Latest Update Note: Clinical Trial Update

Product Description

A long-acting, pegylated, recombinant analog of the endogenous human granulocyte colony-stimulating factor (G-CSF), with hematopoietic activity. Upon administration, mecapegfilgrastim binds to and activates specific cell surface receptors and stimulates neutrophil progenitor proliferation and differentiation, as well as selected neutrophil functions. This may decrease the duration and incidence of chemotherapy-induced neutropenia (CIN). Pegylation significantly increases the therapeutic half-life. (Sourced from: https://www.cancer.gov/publications/dictionaries/cancer-drug/def/mecapegfilgrastim?redirect=true)

Mechanisms of Action: G-CSF Cleaver

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Subcutaneous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Hengrui Pharmaceutical
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Mecapegfilgrastim

Countries in Clinic: China

Active Clinical Trial Count: 1

Highest Development Phases

Phase 2: Breast Cancer|Neutropenia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

SYSKY-2022-105-01

P2

Recruiting

Neutropenia|Breast Cancer

2023-12-01

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