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Completed Phase 3 Interventional

Safety and Efficacy Study of Alfimeprase in Subjects With Occluded Catheters

ClinicalTrials.gov ID: NCT00322270

Public ClinicalTrials.gov record NCT00322270. 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 Oct 22, 2026, 8:51 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 3, Multicenter, Multinational, Open-Label Study to Evaluate the Safety and Efficacy of Alfimeprase in Subjects With Occluded Central Venous Access Devices (SONOMA-3)

Brief summary

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

To evaluate the safety profile of alfimeprase as assessed by monitoring of adverse events, serious adverse events and major bleeding events for up to 120 minutes following the instillation of study drug to an occluded central venous access device.

Study identification

NCT ID
NCT00322270
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ARCA Biopharma, Inc.
Industry
Enrollment
Not listed

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
Jan 2006 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Aug 15, 2008

Started 2006

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Desert Oasis Cancer Center Casa Grande Arizona 85222 —
Cancer Research & Prevention Center Soquel California 95073 —
Bethesda Research Center Boynton Beach Florida 33435 —
Pasco Hernando Oncology Associates Brooksville Florida 34613 —
Mercy Hospital Miami Florida 33133 —
Pasco Hernando Oncology Associate New Port Richey Florida 34652 —
Medical and Surgical Specialists Galesburg Illinois 61401 —
Cancer Center at Blessing Hospital Quincy Illinois 62301 —
Kalamazoo Hematology and Oncology Kalamazoo Michigan 49048 —
Sparrow Cancer Center Lansing Michigan 48912 —
Comprehensive Cancer Care Clinic Jefferson City Missouri 65109 —
The Center for Cancer Care and Research St Louis Missouri 63141 —
UMDNJ-Robert Wood Johnson Medical School New Brunswick New Jersey 08903 —
Dakota Cancer Institute Fargo North Dakota 58103 —
Gabrail Cancer Center Canton Ohio 44718 —
Hematology/Oncology Consultants, Inc. Columbus Ohio 43235 —
Texas Oncology, P.A. Dallas Texas 75230 —
Carilion Gynecology/Oncology Roanoke Virginia 24074 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00322270, 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 Aug 15, 2008 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00322270 live on ClinicalTrials.gov.

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