TrialSignal
Clinical trial intelligence report
Randomized, Double-Blind Study of Peripheral Blood Progenitor Cell (PBPC) Mobilization by Pegfilgrastim or Filgrastim for Autologous Transplantation in Subjects With Hodgkin's or Non-Hodgkin's Lymphoma.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 13, 2026
NCT ID
NCT00066092
Status
COMPLETED
Phase
Phase 2
Sponsor
Amgen
Executive brief
Investment-Ready Snapshot
This clinical trial, sponsored by Amgen, evaluates the efficacy and safety of pegfilgrastim compared to filgrastim for PBPC mobilization in patients with Hodgkin's and non-Hodgkin's lymphoma. Given the established market for G-CSF products, including filgrastim, pegfilgrastim's longer-acting formulation may provide a competitive advantage in terms of patient compliance and treatment convenience. The trial's completion in 2004 positions Amgen to leverage potential market exclusivity and enhance its portfolio in hematology and oncology, particularly in the context of autologous stem cell transplantation. The results could influence treatment guidelines and establish pegfilgrastim as a preferred option, impacting market dynamics and competitive positioning.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00066092
Indication
Lymphoma
Modality
small molecule
Target
Granulocyte Colony-Stimulating Factor (G-CSF) receptor, involved in the mobilization of peripheral blood progenitor cells (PBPC).
Intervention
pegfilgrastim 12 mg, filgrastim, pegfilgrastim 6 mg
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.