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Completed Phase 2 Interventional

Safety and Efficacy of TP10, a Complement Inhibitor, in Adult Women Undergoing Cardiopulmonary Bypass Surgery

ClinicalTrials.gov ID: NCT00082121

Public ClinicalTrials.gov record NCT00082121. 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, 6:47 AM EDT

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

Brief summary

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

The purpose of this study is to determine if the study drug (TP10), which blocks complement release, can reduce such side effects of complement inflammation as chest pain or heart attacks and be taken safely in women who undergo cardiopulmonary bypass surgery.

Study identification

NCT ID
NCT00082121
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Avant Immunotherapeutics
Industry
Enrollment
300 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Apr 2004 (Type not available)
Primary completion
Not listed
Completion
Dec 2005 (Type not available)
Last update posted
Jul 20, 2007

2004 – 2005

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Not listed San Francisco California 94115 —
Not listed Washington D.C. District of Columbia 20010 —
Not listed Gainesville Florida 32610 —
Not listed Orlando Florida 32803 —
Not listed Sarasota Florida 34239 —
Not listed Atlanta Georgia 30342 —
Not listed Chicago Illinois 60612 —
Not listed Towson Maryland 21204 —
Not listed Boston Massachusetts 02118 —
Not listed Springfield Massachusetts 01199 —
Not listed Detroit Michigan 48202 —
Not listed Lansing Michigan 48910 —
Not listed Cincinnati Ohio 45219 —
Not listed Memphis Tennessee 38120 —
Not listed Houston Texas 77030 —
Not listed Danville Virginia 24541 —
Not listed Madison Wisconsin 53792 —
Not listed Milwaukee Wisconsin 53215 —

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 NCT00082121, 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 Jul 20, 2007 · 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 NCT00082121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →