Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

Safety and Efficacy of (PN-152,243)/PN-196,444 in the Prevention of Thrombocytopenia

ClinicalTrials.gov ID: NCT00039910

Public ClinicalTrials.gov record NCT00039910. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 10, 2026, 8:28 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Safety and Efficacy of (PN-152,243)/PN-196,444 in the Prevention of Thrombocytopenia in Recurrent or Refractory Non-Burkitt's, Non-Hodgkin's Lymphoma (NHL) or Hodgkin's Disease Receiving DHAP (Dexamethasone, High-Dose Cytarabine and Cisplatin) Chemotherapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Intensive chemotherapy is associated with significant thrombocytopenia, often requiring platelet transfusion to maintain platelet counts. This investigational drug has been demonstrated to increase platelet counts. This study will test the safety and efficacy of the investigational drug in the prevention of thrombocytopenia in patients with recurrent or refractory intermediate-grade or high-grade non-Burkitt's, non-Hodgkin's lymphoma (NHL), or Hodgkin's disease receiving DHAP (Dexamethasone, high-dose Cytarabine, and Cisplatin) chemotherapy.

Study identification

NCT ID
NCT00039910
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
240 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2000 (Type not available)
Primary completion
Not listed
Completion
Mar 2003 (Actual)
Last update posted
May 4, 2007

2000 – 2003

United States locations

U.S. sites
27
U.S. states
14
U.S. cities
21
Facility City State ZIP Site status
Pfizer Investigational Site Phoenix Arizona 85023 —
Pfizer Investigational Site La Jolla California 92037 —
Pfizer Investigational Site Loma Linda California 92354 —
Pfizer Investigational Site Los Angeles California 90033-0804 —
Pfizer Investigational Site Los Angeles California 90036 —
Pfizer Investigational Site Los Angeles California 90048 —
Pfizer Investigational Site Los Angeles California 90089 —
Pfizer Investigational Site Orange California 92868 —
Pfizer Investigational Site Tamarac Florida 33321 —
Pfizer Investigational Site Chicago Illinois 60637 —
Pfizer Investigational Site Chicago Illinois 60640 —
Pfizer Investigational Site Lake Charles Louisiana 70601 —
Pfizer Investigational Site Detroit Michigan 48202 —
Pfizer Investigational Site Saint Joseph Michigan 49085 —
Pfizer Investigational Site Southfield Michigan 48076 —
Pfizer Investigational Site Jefferson City Missouri 65109 —
Pfizer Investigational Site Jefferson City Missouri 90048 —
Pfizer Investigational Site Omaha Nebraska 68198 —
Pfizer Investigational Site Brooklyn New York 11235 —
Pfizer Investigational Site Durham North Carolina 27705 —
Pfizer Investigational Site Coos Bay Oregon 97420 —
Pfizer Investigational Site Hershey Pennsylvania 17033 —
Pfizer Investigational Site Bristol Tennessee 37620 —
Pfizer Investigational Site Abingdon Virginia 24210 —
Pfizer Investigational Site Abingdon Virginia 24211 —
Pfizer Investigational Site Lebanon Virginia 24266 —
Pfizer Investigational Site Marion Virginia 24354 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00039910, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 4, 2007 · Synced Nov 10, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00039910 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →