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NCT00066092COMPLETEDanonymous

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.

Sponsor

Source record

Amgen

Phase

Source record

Phase 2

Modality

AI-normalized

small molecule

Target

AI-normalized

Granulocyte Colony-Stimulating Factor (G-CSF) receptor, involved in the mobilization of peripheral blood progenitor cells (PBPC).

Indication / condition

AI-normalized

Lymphoma

Intervention

Source record

pegfilgrastim 12 mg, filgrastim, pegfilgrastim 6 mg

Source & freshness

Source record

NCT ID

NCT00066092

Original source

ClinicalTrials.gov

Source last updated

Feb 28, 2008

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT00066092

Title

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.

Sponsor

Amgen

Status

COMPLETED

Phase

Phase 2

Condition raw

Lymphoma, Hodgkin's Lymphoma, Non-Hodgkin's Lymphoma, Hematology, Oncology

Condition normalized

Lymphoma, Hodgkin's Lymphoma, Non-Hodgkin's Lymphoma, Hematology, Oncology

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Granulocyte Colony-Stimulating Factor (G-CSF) receptor, involved in the mobilization of peripheral blood progenitor cells (PBPC).

Target normalized

Granulocyte Colony-Stimulating Factor (G-CSF) receptor, involved in the mobilization of peripheral blood progenitor cells (PBPC).

Interventions

pegfilgrastim 12 mg, filgrastim, pegfilgrastim 6 mg

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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